Page 65«..1020..64656667..7080..»

Aprea Therapeutics Receives FDA Breakthrough Therapy Designation for APR-246 in Combination with Azacitidine for the Treatment of Myelodysplastic…

By daniellenierenberg

BOSTON, Jan. 30, 2020 (GLOBE NEWSWIRE) -- Aprea Therapeutics, Inc. (NASDAQ: APRE), a biopharmaceutical company focused on developing and commercializing novel cancer therapeutics that reactivate mutant tumor suppressor protein p53, today announced that the U.S. Food and Drug Administration (FDA) has granted Breakthrough Therapy Designation for APR-246 in combination with azacitidine for the treatment of myelodysplastic syndromes (MDS) with a susceptible TP53 mutation.

MDS represents a spectrum of hematopoietic stem cell malignancies in which bone marrow fails to produce sufficient numbers of healthy blood cells. Approximately 30-40% of MDS patients progress to acute myeloid leukemia (AML) and mutation of the p53 tumor suppressor protein is thought to directly contribute to disease progression and a poor overall prognosis.

Breakthrough Therapy Designation further supports our development program for APR-246 in combination with azacitidine in MDS patients with a TP53 mutation, said Christian S. Schade, Chief Executive Officer of Aprea. Outcomes for MDS patients with a TP53 mutation are poor and there are no current therapeutic options specifically for these patients. We look forward to continued interaction with FDA regarding our ongoing Phase 3 clinical study and our clinical development program to advance APR-246.

The FDAs Breakthrough Therapy Designation is intended to expedite the development and review of a drug candidate that is planned to treat a serious or life-threatening disease or condition when preliminary clinical evidence indicates that the drug may demonstrate substantial improvement over available therapies on one or more clinically significant endpoints.

About p53 and APR-246

The p53 tumor suppressor gene is the most frequently mutated gene in human cancer, occurring in approximately 50% of all human tumors. These mutations are often associated with resistance to anti-cancer drugs and poor overall survival, representing a major unmet medical need in the treatment of cancer.

APR-246 is a small molecule that has demonstrated reactivation of mutant and inactivated p53 protein by restoring wild-type p53 conformation and function and thereby induce programmed cell death in human cancer cells. Pre-clinical anti-tumor activity has been observed with APR-246 in a wide variety of solid and hematological cancers, including MDS, AML, and ovarian cancer, among others. Additionally, strong synergy has been seen with both traditional anti-cancer agents, such as chemotherapy, as well as newer mechanism-based anti-cancer drugs and immuno-oncology checkpoint inhibitors. In addition to pre-clinical testing, a Phase 1/2 clinical program with APR-246 has been completed, demonstrating a favorable safety profile and both biological and confirmed clinical responses in hematological malignancies and solid tumors with mutations in the TP53 gene.

A pivotal Phase 3 clinical trial of APR-246 and azacitidine for frontline treatment of TP53 mutant MDS is ongoing. APR-246 has received Orphan Drug and Fast Track designations from the FDA for MDS, and Orphan Drug designation from the EMA for MDS, AML and ovarian cancer.

About Aprea Therapeutics

Aprea Therapeutics Inc., (NASDAQ: APRE) is a biopharmaceutical company headquartered in Boston, Massachusetts with research facilities in Stockholm, Sweden, focused on developing and commercializing novel cancer therapeutics that reactivate the mutant tumor suppressor protein p53. The Companys lead product candidate is APR-246, a small molecule in clinical development for hematologic malignancies, including myelodysplastic syndromes (MDS) and acute myeloid leukemia (AML). For more information, please visit the company website at http://www.aprea.com.

The Company may use, and intends to use, its investor relations website at http://www.ir.aprea.com as a means of disclosing material nonpublic information and for complying with its disclosure obligations under Regulation FD.

Forward-Looking Statements

Certain information contained in this press release includes forward-looking statements, within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended, related to our clinical trials and regulatory submissions. We may, in some cases use terms such as predicts, believes, potential, continue, anticipates, estimates, expects, plans, intends, may, could, might, likely, will, should or other words that convey uncertainty of the future events or outcomes to identify these forward-looking statements. Our forward-looking statements are based on current beliefs and expectations of our management team that involve risks, potential changes in circumstances, assumptions, and uncertainties. Any or all of the forward-looking statements may turn out to be wrong or be affected by inaccurate assumptions we might make or by known or unknown risks and uncertainties. These forward-looking statements are subject to risks and uncertainties including risks related to the success and timing of our clinical trials or other studies and the other risks set forth in our filings with the U.S. Securities and Exchange Commission, including our Quarterly Report on Form 10-Q. For all these reasons, actual results and developments could be materially different from those expressed in or implied by our forward-looking statements. You are cautioned not to place undue reliance on these forward-looking statements, which are made only as of the date of this press release. We undertake no obligation to publicly update such forward-looking statements to reflect subsequent events or circumstances.

Corporate Contacts:

Scott M. CoianteSr. Vice President and Chief Financial Officer617-463-9385

Gregory A. KorbelVice President of Business Development617-463-9385

Source: Aprea Therapeutics, Inc.

More here:
Aprea Therapeutics Receives FDA Breakthrough Therapy Designation for APR-246 in Combination with Azacitidine for the Treatment of Myelodysplastic...

To Read More: Aprea Therapeutics Receives FDA Breakthrough Therapy Designation for APR-246 in Combination with Azacitidine for the Treatment of Myelodysplastic…
categoriaBone Marrow Stem Cells commentoComments Off on Aprea Therapeutics Receives FDA Breakthrough Therapy Designation for APR-246 in Combination with Azacitidine for the Treatment of Myelodysplastic… | dataJanuary 30th, 2020
Read All

Cell Transplant Market 2020 In Depth Research, Size, Trends and Forecast by 2026 | Regen Biopharma, Global Cord Blood Corporation, CBR Systems -…

By daniellenierenberg

The report helps players and investors to stay in a competent position in the global Cell Transplant market as they gain insights into the market competition, leading segments, top regions, and other vital subjects.

The report on the global Cell Transplant market is just the resource that players need to strengthen their overall growth and establish a strong position in their business. It is a compilation of detailed, accurate research studies that provide in-depth analysis on critical subjects of the global Cell Transplant market such as consumption, revenue, sales, production, trends, opportunities, geographic expansion, competition, segmentation, growth drivers, and challenges.

Get the Sample of this [emailprotected]https://www.qyresearch.com/sample-form/form/1495010/global-cell-transplant-market

As part of geographic analysis of the global Cell Transplant market, the report digs deep into the growth of key regions and countries, including but not limited to North America, the US, Europe, the UK, Germany, France, Asia Pacific, China, and the MEA. All of the geographies are comprehensively studied on the basis of share, consumption, production, future growth potential, CAGR, and many other parameters.

Market Segments Covered:

The key players covered in this studyRegen BiopharmaGlobal Cord Blood CorporationCBR SystemsEscape TherapeuticsCryo-SaveLonza GroupPluristem TherapeuticsStemedica Cell Technology

Market segment by Type, the product can be split intoPeripheral Blood Stem Cells Transplant (PBSCT)Bone Marrow Transplant (BMT)Cord Blood Transplant (CBT)

Market segment by Application, split intoHospitalsClinicsOthers

Regions Covered in the Global Cell Transplant Market:

The Middle East and Africa (GCC Countries and Egypt) North America (the United States, Mexico, and Canada) South America (Brazil etc.) Europe (Turkey, Germany, Russia UK, Italy, France, etc.) Asia-Pacific (Vietnam, China, Malaysia, Japan, Philippines, Korea, Thailand, India, Indonesia, and Australia)

Highlights of the Report Accurate market size and CAGR forecasts for the period 2019-2025 Identification and in-depth assessment of growth opportunities in key segments and regions Detailed company profiling of top players of the global Cell Transplant market Exhaustive research on innovation and other trends of the global Cell Transplant market Reliable industry value chain and supply chain analysis Comprehensive analysis of important growth drivers, restraints, challenges, and growth prospects

The scope of the Report:

The report offers a complete company profiling of leading players competing in the global Cell Transplant market with high focus on share, gross margin, net profit, sales, product portfolio, new applications, recent developments, and several other factors. It also throws light on the vendor landscape to help players become aware of future competitive changes in the global Cell Transplant market.

Get Customized Report in your Inbox within 24 hours @https://www.qyresearch.com/customize-request/form/1495010/global-cell-transplant-market

Strategic Points Covered in TOC:

Chapter 1: Introduction, market driving force product scope, market risk, market overview, and market opportunities of the global Cell Transplant market

Chapter 2: Evaluating the leading manufacturers of the global Cell Transplant market which consists of its revenue, sales, and price of the products

Chapter 3: Displaying the competitive nature among key manufacturers, with market share, revenue, and sales

Chapter 4: Presenting global Cell Transplant market by regions, market share and with revenue and sales for the projected period

Chapter 5, 6, 7, 8 and 9 : To evaluate the market by segments, by countries and by manufacturers with revenue share and sales by key countries in these various regions

About Us:QYResearch always pursuits high product quality with the belief that quality is the soul of business. Through years of effort and supports from huge number of customer supports, QYResearch consulting group has accumulated creative design methods on many high-quality markets investigation and research team with rich experience. Today, QYResearch has become the brand of quality assurance in consulting industry.

Continue reading here:
Cell Transplant Market 2020 In Depth Research, Size, Trends and Forecast by 2026 | Regen Biopharma, Global Cord Blood Corporation, CBR Systems -...

To Read More: Cell Transplant Market 2020 In Depth Research, Size, Trends and Forecast by 2026 | Regen Biopharma, Global Cord Blood Corporation, CBR Systems -…
categoriaBone Marrow Stem Cells commentoComments Off on Cell Transplant Market 2020 In Depth Research, Size, Trends and Forecast by 2026 | Regen Biopharma, Global Cord Blood Corporation, CBR Systems -… | dataJanuary 30th, 2020
Read All

Cancer patient flies dad who saved his life 6600 miles away around the world – Birmingham Live

By daniellenierenberg

A dad who saved the life of a cancer patient 6,600 miles away was flown around the world on a trip of a lifetime by his grateful recipient - who tracked him down.

Milton Becker, 69, was close to death and in desperate need of a bone marrow donor when a two-and-a-half year global search linked him with an anonymous Welsh man.

Emyr Williams, 54, was a near-perfect match, and his bone marrow was flown to Canada and given to Milton, who was declared cancer free.

The pair were linked up by the donation database and grew close via phone calls and Facebook messages.

And last year he invited retired carpenter Emyr to Canada for a two week body">

A dad who saved the life of a cancer patient 6,600 miles away was flown around the world on a trip of a lifetime by his grateful recipient - who tracked him down.

Milton Becker, 69, was close to death and in desperate need of a bone marrow donor when a two-and-a-half year global search linked him with an anonymous Welsh man.

Emyr Williams, 54, was a near-perfect match, and his bone marrow was flown to Canada and given to Milton, who was declared cancer free.

The pair were linked up by the donation database and grew close via phone calls and Facebook messages.

And last year he invited retired carpenter Emyr to Canada for a two week $15,000 (8,835) trip around Alberta and the Rocky Mountains.

Meeting him for the first time at the airport, wearing a Welsh dragon T-shirt and a Wales flag, they formed an instant bond.

Milton said he's "indebted" to his hero - and is planning a UK trip.

Dad-of-three Emyr, from Lampeter, Wales, said: "It was surreal to be out there.

"There's this bond between us like no other.

"It was only when we went out there that we really understood how close to death Milton was.

"One of his friends said he had been finalising plans to be at his funeral.

"He was literally on death's door.

"For something that required no real effort at all saved that great man's life.

"And to have the pleasure of meeting him in the flesh and to be introduced to his family was just an honour."

Granddad-of-two Milton, from Alberta, Canada, added: "We got on so well and I just thought I've got to thank this guy.

"I didn't want him to spend a penny. It was my treat.

"It's not about the money. What he did was priceless.

"I'm forever indebted to the guy."

Milton was diagnosed with stage 4 leukaemia in 2010 but after unsuccessful chemotherapy he was told a bone marrow transplant was the only means of survival.

Doctors searched across Canada but were unsuccessful and begun their two-and-a-half year worldwide search for a donor.

In early 2013, Emyr - who had been registered on the blood transfusion register for several years - was found to be a near-perfect match.

Emyr said: "A lady called me one day to say 'would you be interested in donating your stem cells?

"She went on to say there was a guy in Canada with leukaemia and that I was a 99.9999 per cent match with him.

"I just thought why not.

"It doesn't cost me anything and it can really change somebody's life."

The bone marrow was flown from Wales - with Milton receiving his long-awaited transfusion on his 63rd birthday, on 1st February 2013.

Former oil company lorry driver Milton said: "What he did was completely priceless.

"There's no better gift than the gift of life.

"And to get that on my birthday, well, it was a great feeling!"

A year after the transfusion Milton was told he was on the road to recovery but was kept in remission and monitored by doctors for the next two years.

In 2016, three years after the blood transfusion, Milton was deemed cancer-free.

It led nurses to ask Milton if he would like to know who his donor was - which he accepted straight away.

They got in touch with Emyr - who'd been given bi-annual anonymous updates - who agreed his details could be passed on.

Emyr said: "A few days later I had this call from an international number.

"I remember it as clear as day.

"He phoned me up and said; 'Emyr, my name is Milton and I just want to say how thankful I am'.

"From then on we just hit it off.

"What makes me laugh is he always forgets his Facebook password so he's a complete technophobe.

"We speak through his children on Facebook.

"We mostly speak about our family."

Milton said: "I couldn't turn up the chance to thank the guy who gave me life!

"I started off by thanking him and we had a great chat.

"I told him I would be forever grateful and wanted to keep in touch."

The two then added each other on Facebook and soon became good friends with weekly messages and monthly phone calls.

Then two years later Milton phoned Emyr to ask if he and his family would be interested in flying out to Canada for a two-week holiday.

Emyr said: "He asked me during one of our phone calls.

"I had never been to Canada and thought it would just be great to meet each other face-to-face."

Emyr flew out with his wife and teenage daughter last September 2019 to start the two-week itinerary around Alberta and the Rocky Mountains.

Emyr said: "He was there at the airport with a Welsh dragon on his T-shirt and a Welsh flag.

"You couldn't miss them.

"We have beautiful mountains here in Wales but Canada was just something else.

"It was an absolutely incredible trip.

"He paid for it all.

"We stayed in cabins, had a party with his extended family, we drank, sat by the open fire, and toasted marshmallows."

Milton added: "One Sunday I took him to my church.

"People knew he was coming and the service and to my surprise Emyr got up and told the church about the successful operation.

"There were tears but it was just beautiful."

Now seven years on from the transfusion, the pair say they are thankful to have one another in each other's lives.

The pair still keep regular contact with one another, with Facebook messages, fortnightly phone calls and even FaceTimed each other on Christmas Day.

Emyr said: "They're planning on coming to Wales next year in June or July.

"We'll definitely go back out there again in a few years.

"Even though we're thousands of miles away, we're such great friends."

Milton said: "We still have our chit-chats and I'd love to go over to the UK.

5,000 (8,835) trip around Alberta and the Rocky Mountains.

Meeting him for the first time at the airport, wearing a Welsh dragon T-shirt and a Wales flag, they formed an instant bond.

Milton said he's "indebted" to his hero - and is planning a UK trip.

Dad-of-three Emyr, from Lampeter, Wales, said: "It was surreal to be out there.

"There's this bond between us like no other.

"It was only when we went out there that we really understood how close to death Milton was.

"One of his friends said he had been finalising plans to be at his funeral.

"He was literally on death's door.

"For something that required no real effort at all saved that great man's life.

"And to have the pleasure of meeting him in the flesh and to be introduced to his family was just an honour."

Granddad-of-two Milton, from Alberta, Canada, added: "We got on so well and I just thought I've got to thank this guy.

"I didn't want him to spend a penny. It was my treat.

"It's not about the money. What he did was priceless.

"I'm forever indebted to the guy."

Milton was diagnosed with stage 4 leukaemia in 2010 but after unsuccessful chemotherapy he was told a bone marrow transplant was the only means of survival.

Doctors searched across Canada but were unsuccessful and begun their two-and-a-half year worldwide search for a donor.

In early 2013, Emyr - who had been registered on the blood transfusion register for several years - was found to be a near-perfect match.

Emyr said: "A lady called me one day to say 'would you be interested in donating your stem cells?

"She went on to say there was a guy in Canada with leukaemia and that I was a 99.9999 per cent match with him.

"I just thought why not.

"It doesn't cost me anything and it can really change somebody's life."

The bone marrow was flown from Wales - with Milton receiving his long-awaited transfusion on his 63rd birthday, on 1st February 2013.

Former oil company lorry driver Milton said: "What he did was completely priceless.

"There's no better gift than the gift of life.

"And to get that on my birthday, well, it was a great feeling!"

A year after the transfusion Milton was told he was on the road to recovery but was kept in remission and monitored by doctors for the next two years.

In 2016, three years after the blood transfusion, Milton was deemed cancer-free.

It led nurses to ask Milton if he would like to know who his donor was - which he accepted straight away.

They got in touch with Emyr - who'd been given bi-annual anonymous updates - who agreed his details could be passed on.

Video Unavailable

Click to playTap to play

Play now

Read more from the original source:
Cancer patient flies dad who saved his life 6600 miles away around the world - Birmingham Live

To Read More: Cancer patient flies dad who saved his life 6600 miles away around the world – Birmingham Live
categoriaBone Marrow Stem Cells commentoComments Off on Cancer patient flies dad who saved his life 6600 miles away around the world – Birmingham Live | dataJanuary 30th, 2020
Read All

After a bone injury, shape-shifting cells rush to the rescue – University of Michigan News

By daniellenierenberg

ANN ARBORConventional thinking is that bone regeneration is left to a small number of mighty cells called skeletal stem cells, which reside within larger groups of bone marrow stromal cells.

But new findings from the University of Michigan recasts that thinking.

In a recent study, Noriaki Ono, assistant professor at the U-M School of Dentistry, and colleagues report that mature bone marrow stromal cells metamorphosed to perform in ways similar to their bone-healing stem cell cousinsbut only after an injury.

Bone fracture is an emergency for humans and all vertebrates, so the sooner cells start the business of healing damaged boneand the more cells there are to do itthe better.

Our study shows that other cells besides skeletal stem cells can do this job as well, Ono said.

In the mouse study, inert Cxcl12 cells in bone marrow responded to post-injury cellular cues by converting into regenerative cells, much like skeletal stem cells. Normally, the main job of these Cxcl12-expressing cells, widely known as CAR cells, is to secrete cytokines, which help regulate neighboring blood cells. They were recruited for healing only after an injury.

The surprise in our study is that these cells essentially did nothing in terms of making bones, when bones grow longer, Ono said. Its only when bones are injured that these cells start rushing to repair the defect.

This is important because the remarkable regenerative potential of bones is generally attributed to rare skeletal stem cells, Ono says. These new findings raise the possibility that these mighty skeletal stem cells could be generated through the transformation of the more available mature stromal cells.

These mature stromal cells are malleable and readily available throughout life, and could potentially provide an excellent cellular source for bone and tissue regeneration, Ono says.

The study appears in the journal Nature Communications.

More information:

View post:
After a bone injury, shape-shifting cells rush to the rescue - University of Michigan News

To Read More: After a bone injury, shape-shifting cells rush to the rescue – University of Michigan News
categoriaBone Marrow Stem Cells commentoComments Off on After a bone injury, shape-shifting cells rush to the rescue – University of Michigan News | dataJanuary 30th, 2020
Read All

What are Progenitor Cells? Exploring Neural, Myeloid and Hematopoietic Progenitor Cells – Technology Networks

By daniellenierenberg

What are progenitor cells?

Every cell in the human body, and that of other mammals, originates from stem cell precursors. Progenitor cells are descendants of stem cells that then further differentiate to create specialized cell types.There are many types of progenitor cells throughout the human body. Each progenitor cell is only capable of differentiating into cells that belong to the same tissue or organ. Some progenitor cells have one final target cell that they differentiate to, while others have the potential to terminate in more than one cell type.

Stem cells share two qualifying characteristics. Firstly, all stem cells have the potential to differentiate into multiple types of cells. Secondly, stem cells are capable of unlimited self-replication via asymmetric cell division, a process known as self-renewal.There are two broad categories of stem cells found in all mammals. The first are embryonic stem cells. These cells arise from the inner cell mass of the blastocyst in an early-stage embryo. Embryonic stem cells are the blueprint used to create every cell in the body. Because they can be used to create any type of cell, they are known as pluripotent.

The second type of stem cells found in mammals are adult stem cells (or somatic stem cells). Unlike pluripotent embryonic stem cells, adult stem cells are more limited in relation to the type of cells that they become. Unlike embryonic stem cells that could be used to create any cell, adult stem cells are limited to generating cell types within a specific lineage, such as blood cells or cells of the central nervous system. This level of differentiation potential is termed multipotent.

Stem cells create two types of progeny: more stem cells or progenitor cells. All progenitor cells are descendants of stem cells. When it comes to cell differentiation, they fall on the spectrum between stem cells and fully differentiated (mature) cells.

Whilst stem cells have indefinite replication (left) progenitor cells can at most differentiate into multiple types of specialized cell (right).

Function:

Cellular repair or maintenance

Cell Potency:

Multipotent, oligopotent, or unipotent

Self-renewal:

Limited

Origin:

Stem cells

Creates:

Further differentiated cells (either progenitor cells of mature/fully differentiated cells)

Progenitor cells are an intermediary step involved in the creation of mature cells in human tissues and organs, the blood, and the central nervous system.

The human central nervous system (CNS) contains three types of fully differentiated cells: neurons, astrocytes and oligodendrocytes. The latter two are collectively known as glial cells.Every neuron, oligodendrocyte and astrocyte in the CNS evolves from the differentiation of neural progenitor cells (NPCs). NPCs themselves are produced by multipotent neural stem cells (NSCs). Both NPCs and NSCs are termed neural precursor cells.Before the 1990s, it was believed that neurogenesis terminated early in life. More recent studies demonstrate that the brain contains stem cells that are capable of regenerating neurons and glial cells throughout the human lifecycle. These stem cells have only been found in certain brain regions, including the striatum and lateral ventricle.

Hematopoietic progenitor cells (HPCs) are an intermediate cell type in blood cell development. HPCs are immature cells that develop from hematopoietic stem cells, cells that can both self-renew and differentiate into hematopoietic progenitor cells. HPCs eventually differentiate into one of more than ten different types of mature blood cells.Hematopoietic progenitor cells are categorized based upon their cell potency, or their differentiation potential. As blood cells develop, their potency decreases.

First, hematopoietic stem cells differentiate into multipotent progenitor cells. Multipotent progenitor cells are those with the potential to differentiate into a subset of cell types. These cells then differentiate into either the common myeloid progenitor (CMP) or common lymphoid progenitor (CLP). Both CMPs and CLPs are types of oligopotent progenitor cells (progenitor cells that differentiate into only a few cell types).

CMPs and CLPs continue to differentiate along cell lines into lineage-restricted progenitor cells that become final, mature blood cells.Myeloid progenitor cells are precursors to the following types of blood cells:

Lymphoid progenitor cells (also known as lymphoblasts) are precursors to other mature blood cell types, including:

The primary role of progenitor cells is to replace dead or damaged cells. In this way, progenitor cells are necessary for repair after injury and as part of ongoing tissue maintenance. Progenitor cells also replenish blood cells and play a role in embryonic development.

Neural progenitor cells (NPCs) are being explored alongside neural stem cells for their potential to treat diseases of or injury to the central nervous system. A deeper understanding of how these cells function on a cellular and molecular basis is needed to progress from early experimental research to therapeutic use.NPCs are currently utilized in research conducted on CNS disorders, development, cell regeneration and degeneration, neuronal excitability, and therapy screening. When compared to induced pluripotent stem cells, which are cells reprogrammed into a pluripotent state, NPCs can cut down on time in some experiments.Hematopoietic progenitor cells and stem cells are being researched for their capacity to treat blood cell disorders. They are also currently used to help treat patients with a variety of malignant and non-malignant diseases via bone marrow transplants that deliver bone marrow and peripheral blood progenitor cells to patients. These procedures can assist patients in recovering from the damage caused by chemotherapy.Additionally, researchers are examining the potential of using progenitor cells to create a variety of tissues, such as blood vessels, heart valves, and electrically conductive tissue for the cardiovascular system.

View original post here:
What are Progenitor Cells? Exploring Neural, Myeloid and Hematopoietic Progenitor Cells - Technology Networks

To Read More: What are Progenitor Cells? Exploring Neural, Myeloid and Hematopoietic Progenitor Cells – Technology Networks
categoriaBone Marrow Stem Cells commentoComments Off on What are Progenitor Cells? Exploring Neural, Myeloid and Hematopoietic Progenitor Cells – Technology Networks | dataJanuary 28th, 2020
Read All

The Benefit of Adding Daratumumab to Multiple Myeloma Drug Combinations – SurvivorNet

By daniellenierenberg

Daratumumab: A Promising Option

Due to promising new data from several big clinical trials, its now believed that daratumumab can benefit patients with multiple myeloma regardless ofwhether theyre eligible to receive a stem cell transplant.

Daratumumab (also known by its brand name, Darzalex), is a type of drug called a targeted monoclonal antibody. It works by binding to a specific protein called CD38, which is found on the surface of multiple myeloma cells. Once the daratumumab attaches to these proteins on the surface of the cells, the bodys immune system identifies the need to attack and kill the multiple myeloma cells.

As Dr. Nina Shah,a hematologist at the University of California San Francisco, explains, patients receiving a stem cell transplant can benefit from the addition of daratumumab to a combination of the drugs Velcade, Revlimid and dexamethasone (a combination that doctors often abbreviate as Dara VRD).

If, on the other hand, a transplant isnt the right course of treatment for you, you may still be able to benefit from daratumumab when its used in whats called the upfront or first-line treatment setting (meaning as the first part of your treatment, before you receive other drugs) when combined withRevlimid and dexamethasone (a combination that doctors often abbreviate as DRD).

If youre not interested in a transplant, or maybe thats not in the works for you at the moment, you may consider daratumumab, Revlimid and dexamethasone, or DRD,' Dr. Shah explains.

One thing thats really gotten a lot of attention is not just three drugs, but four drugs, Dr. Shah says. She explains that a recent clinical trial called GRIFFIN showed that before a stem cell transplant, treatment with daratumumab in combination with Velcade, Revlimid and dexamethasone was more beneficial than treatment with Velcade, Revlimid and dexamethasone alone.

And when patients who received this combination before their transplant, then went on to receive additional daratumumab after their transplant, the benefit was even greater.

Preliminarily, at least, the data seems to indicate that the patients who got four drugs, then went on to a transplant and then got more daratumumab actually did better than the three drugs, Dr. Shah says.

Learn more about SurvivorNet's rigorous medical review process.

Dr. Nina Shah is a hematologist who specializes in the treatment of multiple myeloma, a type of cancer affecting the blood marrow. She treats patients at the Hematology and Blood and Marrow Transplant Clinic. Read More

Daratumumab (also known by its brand name, Darzalex), is a type of drug called a targeted monoclonal antibody. It works by binding to a specific protein called CD38, which is found on the surface of multiple myeloma cells. Once the daratumumab attaches to these proteins on the surface of the cells, the bodys immune system identifies the need to attack and kill the multiple myeloma cells.

If, on the other hand, a transplant isnt the right course of treatment for you, you may still be able to benefit from daratumumab when its used in whats called the upfront or first-line treatment setting (meaning as the first part of your treatment, before you receive other drugs) when combined withRevlimid and dexamethasone (a combination that doctors often abbreviate as DRD).

If youre not interested in a transplant, or maybe thats not in the works for you at the moment, you may consider daratumumab, Revlimid and dexamethasone, or DRD,' Dr. Shah explains.

One thing thats really gotten a lot of attention is not just three drugs, but four drugs, Dr. Shah says. She explains that a recent clinical trial called GRIFFIN showed that before a stem cell transplant, treatment with daratumumab in combination with Velcade, Revlimid and dexamethasone was more beneficial than treatment with Velcade, Revlimid and dexamethasone alone.

And when patients who received this combination before their transplant, then went on to receive additional daratumumab after their transplant, the benefit was even greater.

Preliminarily, at least, the data seems to indicate that the patients who got four drugs, then went on to a transplant and then got more daratumumab actually did better than the three drugs, Dr. Shah says.

Learn more about SurvivorNet's rigorous medical review process.

Dr. Nina Shah is a hematologist who specializes in the treatment of multiple myeloma, a type of cancer affecting the blood marrow. She treats patients at the Hematology and Blood and Marrow Transplant Clinic. Read More

Link:
The Benefit of Adding Daratumumab to Multiple Myeloma Drug Combinations - SurvivorNet

To Read More: The Benefit of Adding Daratumumab to Multiple Myeloma Drug Combinations – SurvivorNet
categoriaBone Marrow Stem Cells commentoComments Off on The Benefit of Adding Daratumumab to Multiple Myeloma Drug Combinations – SurvivorNet | dataJanuary 28th, 2020
Read All

Europe’s guardian of stem cells and hopes, real and unrealistic – INQUIRER.net

By daniellenierenberg

Submerged in liquid nitrogen vapor at a temperature of minus 175 degrees Celsius, hundreds of thousands of stem cells from all over Europe bide their time in large steel barrels on the outskirts of Warsaw.

Present in blood drawn from the umbilical cord of a newborn baby, stem cells can help cure serious blood-related illnesses like leukemias and lymphomas, as well as genetic conditions and immune system deficits.

Polish umbilical cord blood bank PBKM/FamiCord became the industrys leader in Europe after Swiss firm Cryo-Save went bankrupt early last year.

It is also the fifth largest in the world, according to its management, after two companies in the United States, a Chinese firm and one based in Singapore.

Since the first cord blood transplant was performed in France in 1988, the sector has significantly progressed, fuelling hopes.

Health insurance

Mum-of-two Teresa Przeborowska has firsthand experience.

At five years old, her son Michal was diagnosed with lymphoblastic leukemia and needed a bone marrow transplant, the entrepreneur from northern Poland said.

The most compatible donor was his younger sister, Magdalena.

When she was born, her parents had a bag of her cord blood stored at PBKM.

More than three years later, doctors injected his sisters stem cells into Michals bloodstream.

It was not quite enough for Michals needs but nicely supplemented harvested bone marrow.

As a result, Michal, who is nine, is now flourishing, both intellectually and physically, his mum told AFP.

A cord blood transplant has become an alternative to a bone marrow transplant when there is no donor available, with a lower risk of complications.

Stem cells taken from umbilical cord blood are like those taken from bone marrow, capable of producing all blood cells: red cells, platelets and immune system cells.

When used, stem cells are first concentrated, then injected into the patient. Once transfused, they produce new cells of every kind.

At the PBKM laboratory, each container holds up to 10,000 blood bags Safe and secure, they wait to be used in the future, its head, Krzysztof Machaj, said.

The bank holds around 440,000 samples, not including those from Cryo-Save, he said.

If the need arises, the blood will be ready to use without the whole process of looking for a compatible donor and running blood tests, the biologist told AFP.

For families who have paid an initial nearly 600 euros (around P34,000) and then an annual 120 euros (around P7,000) to have the blood taken from their newborns umbilical cords preserved for around 20 years, it is a kind of health insurance promising faster and more effective treatment if illness strikes.

But researchers also warn against unrealistic expectations.

Beauty products

Hematologist Wieslaw Jedrzejczak, a bone marrow pioneer in Poland, describes promoters of the treatment as sellers of hope, who make promises that are either impossible to realize in the near future or downright impossible to realize at all for biological reasons.

He compares them to makers of beauty products who swear their cream will rejuvenate the client by 20 years.

Various research is being done on the possibility of using the stem cells to treat other diseases, notably nervous disorders. But the EuroStemCell scientist network warns that the research is not yet conclusive.

There is a list of almost 80 diseases for which stem cells could prove beneficial, U.S. hematologist Roger Mrowiec, who heads the clinical laboratory of the cord blood program Vitalant in New Jersey, told AFP.

But given the present state of medicine, they are effective only for around a dozen of them, like leukemia or cerebral palsy, he said.

Its not true, as its written sometimes, that we can already use them to fight Parkinsons disease or Alzheimers disease or diabetes.

EuroStemCell also cautions against private blood banks that advertise services to parents suggesting they should pay to freeze their childs cord blood in case its needed later in life.

Studies show it is highly unlikely that the cord blood will ever be used for their child, the network said.

It also pointed out that there could be a risk of the childs cells not being useable anyway without reintroducing the same illness.

Some countries, such as Belgium and France, are cautious and ban the storage of cord blood for private purposes. Most E.U. countries however permit it while imposing strict controls.

Rapid growth

In the early 2000s, Swiss company Cryo-Save enjoyed rapid growth.

Greeks, Hungarians, Italians, Spaniards and Swiss stored blood from their newborns with the company for 20 years on payment of 2,500 euros (around P140,000) upfront.

When the firm was forced to close in early 2019, clients were left wondering where their stem cells would end up.

Under a kind of back-up agreement, the samples of some 250,000 European families were transferred for storage at PBKM.

The Polish firm, founded in 2002 with 2 million zlotys (around P26 million), has also grown quickly.

Present under the FamiCord brand in several countries, PBKM has some 35% of the European market, excluding Cryo-Save assets.

Over the last 15 months, outside investors have contributed 63 million euros to the firm, PBKMs chief executive Jakub Baran told AFP.

But the company has not escaped controversy: the Polityka weekly recently published a critical investigative report on several private clinics that offer what was described as expensive treatment involving stem cells held by PBKM.IB/JB

RELATED STORIES:

2019: The year gene therapy came of age

Landmark trial finds stem cell treatment reduces disability for those with multiple sclerosis

View original post here:
Europe's guardian of stem cells and hopes, real and unrealistic - INQUIRER.net

To Read More: Europe’s guardian of stem cells and hopes, real and unrealistic – INQUIRER.net
categoriaBone Marrow Stem Cells commentoComments Off on Europe’s guardian of stem cells and hopes, real and unrealistic – INQUIRER.net | dataJanuary 27th, 2020
Read All

Global Cell Therapy Technologies Market : Industry Analysis and Forecast (2018-2026) – Expedition 99

By daniellenierenberg

Global Cell Therapy Technologies Marketwas valued US$ 12 billion in 2018 and is expected to reach US$ 35 billion by 2026, at CAGR of 12.14 %during forecast period.

The objective of the report is to present comprehensive assessment projections with a suitable set of assumptions and methodology. The report helps in understanding Global Cell Therapy Technologies Market dynamics, structure by identifying and analyzing the market segments and projecting the global market size. Further, the report also focuses on the competitive analysis of key players by product, price, financial position, growth strategies, and regional presence. To understand the market dynamics and by region, the report has covered the PEST analysis by region and key economies across the globe, which are supposed to have an impact on market in forecast period. PORTERs analysis, and SVOR analysis of the market as well as detailed SWOT analysis of key players has been done to analyze their strategies. The report will to address all questions of shareholders to prioritize the efforts and investment in the near future to the emerging segment in the Global Cell Therapy Technologies Market.

REQUEST FOR FREE SAMPLE REPORT:https://www.maximizemarketresearch.com/request-sample/31531

Global Cell Therapy Technologies Market: OverviewCell therapy is a transplantation of live human cells to replace or repair damaged tissue and/or cells. With the help of new technologies, limitless imagination, and innovative products, many different types of cells may be used as part of a therapy or treatment for different types of diseases and conditions. Celltherapy technologies plays key role in the practice of medicine such as old fashioned bone marrow transplants is replaced by Hematopoietic stem cell transplantation, capacity of cells in drug discovery. Cell therapy overlap with different therapies like, gene therapy, tissue engineering, cancer vaccines, regenerative medicine, and drug delivery. Establishment of cell banking facilities and production, storage, and characterization of cells are increasing volumetric capabilities of the cell therapy market globally. Initiation of constructive guidelines for cell therapy manufacturing and proven effectiveness of products, these are primary growth stimulants of the market.

Global Cell Therapy Technologies Market: Drivers and RestraintsThe growth of cell therapy technologies market is highly driven by, increasing demand for clinical trials on oncology-oriented cell-based therapy, demand for advanced cell therapy instruments is increasing, owing to its affordability and sustainability, government and private organization , investing more funds in cell-based research therapy for life-style diseases such as diabetes, decrease in prices of stem cell therapies are leading to increased tendency of buyers towards cell therapy, existing companies are collaborating with research institute in order to best fit into regulatory model for cell therapies.Moreover, Healthcare practitioners uses stem cells obtained from bone marrow or blood for treatment of patients with cancer, blood disorders, and immune-related disorders and Development in cell banking facilities and resultant expansion of production, storage, and characterization of cells, these factors will drive the market of cell therapy technologies during forecast period.

On the other hand, the high cost of cell-based research and some ethical issue & legally controversial, are expected to hamper market growth of Cell Therapy Technologies during the forecast period

AJune 2016, there were around 351 companies across the U.S. that were engaged in advertising unauthorized stem cell treatments at their clinics. Such clinics boosted the revenue in this market.in August 2017, the U.S. FDA announced increased enforcement of regulations and oversight of clinics involved in practicing unapproved stem cell therapies. This might hamper the revenue generation during the forecast period; nevertheless, it will allow safe and effective use of stem cell therapies.

Global Cell Therapy Technologies Market: Segmentation AnalysisOn the basis of product, the consumables segment had largest market share in 2018 and is expected to drive the cell therapy instruments market during forecast period at XX % CAGR owing to the huge demand for consumables in cell-based experiments and cancer research and increasing number of new product launches and consumables are essential for every step of cell processing. This is further expected to drive their adoption in the market. These factors will boost the market of Cell Therapy Technologies Market in upcoming years.

On the basis of process, the cell processing had largest market share in 2018 and is expected to grow at the highest CAGR during the forecast period owing to in cell processing stage,a use of cell therapy instruments and media at highest rate, mainly in culture media processing. This is a major factor will drive the market share during forecast period.

Global Cell Therapy Technologies Market: Regional AnalysisNorth America to held largest market share of the cell therapy technologies in 2018 and expected to grow at highest CAGR during forecast period owing to increasing R&D programs in the pharmaceutical and biotechnology industries. North America followed by Europe, Asia Pacific and Rest of the world (Row).

DO INQUIRY BEFORE PURCHASING REPORT HERE:https://www.maximizemarketresearch.com/inquiry-before-buying/31531

Scope of Global Cell Therapy Technologies Market

Global Cell Therapy Technologies Market, by Product

Consumables Equipment Systems & SoftwareGlobal Cell Therapy Technologies Market, by Cell Type

Human Cells Animal CellsGlobal Cell Therapy Technologies Market, by Process Stages

Cell Processing Cell Preservation, Distribution, and Handling Process Monitoring and Quality ControlGlobal Cell Therapy Technologies Market, by End Users

Life Science Research Companies Research InstitutesGlobal Cell Therapy Technologies Market, by Region

North America Europe Asia Pacific Middle East & Africa South America

Key players operating in the Global Cell Therapy Technologies Market

Beckman Coulter, Inc. Becton Dickinson and Company GE Healthcare Lonza Merck KGaA MiltenyiBiotec STEMCELL Technologies, Inc. Terumo BCT, Inc. Thermo Fisher Scientific, Inc. Sartorius AG

Browse Full Report with Facts and Figures of Cell Therapy Technologies Market Report at:https://www.maximizemarketresearch.com/market-report/global-cell-therapy-technologies-market/31531/

MAJOR TOC OF THE REPORT

Chapter One: Cell Therapy Technologies Market Overview

Chapter Two: Manufacturers Profiles

Chapter Three: Global Cell Therapy Technologies Market Competition, by Players

Chapter Four: Global Cell Therapy Technologies Market Size by Regions

Chapter Five: North America Cell Therapy Technologies Revenue by Countries

Chapter Six: Europe Cell Therapy Technologies Revenue by Countries

Chapter Seven: Asia-Pacific Cell Therapy Technologies Revenue by Countries

Chapter Eight: South America Cell Therapy Technologies Revenue by Countries

Chapter Nine: Middle East and Africa Revenue Cell Therapy Technologies by Countries

Chapter Ten: Global Cell Therapy Technologies Market Segment by Type

Chapter Eleven: Global Cell Therapy Technologies Market Segment by Application

Chapter Twelve: Global Cell Therapy Technologies Market Size Forecast (2019-2026)

About Us:

Maximize Market Research provides B2B and B2C market research on 20,000 high growth emerging technologies & opportunities in Chemical, Healthcare, Pharmaceuticals, Electronics & Communications, Internet of Things, Food and Beverages, Aerospace and Defense and other manufacturing sectors.

Contact info:

Name: Vikas Godage

Organization: MAXIMIZE MARKET RESEARCH PVT. LTD.

Email: sales@maximizemarketresearch.com

Contact: +919607065656/ +919607195908

Website:www.maximizemarketresearch.com

See the original post:
Global Cell Therapy Technologies Market : Industry Analysis and Forecast (2018-2026) - Expedition 99

To Read More: Global Cell Therapy Technologies Market : Industry Analysis and Forecast (2018-2026) – Expedition 99
categoriaBone Marrow Stem Cells commentoComments Off on Global Cell Therapy Technologies Market : Industry Analysis and Forecast (2018-2026) – Expedition 99 | dataJanuary 27th, 2020
Read All

Six patients with rare blood disease are doing well after gene therapy clinical trial – Mirage News

By daniellenierenberg

UCLA Broad Stem Cell Research Center/Nature Medicine

At left, image shows white blood cells (red) from one of the X-CGD clinical trial participants before gene therapy. At right, after gene therapy, white blood cells from the same patient show the presence of the chemicals (blue) needed to attack and destroy bacteria and fungus.

UCLA researchers are part of an international team that reported the use of a stem cell gene therapy to treat nine people with the rare, inherited blood disease known as X-linked chronic granulomatous disease, or X-CGD. Six of those patients are now in remission and have stopped other treatments. Before now, people with X-CGD which causes recurrent infections, prolonged hospitalizations for treatment, and a shortened lifespan had to rely on bone marrow donations for a chance at remission.

With this gene therapy, you can use a patients own stem cells instead of donor cells for a transplant, said Dr. Donald Kohn, a member of the Eli and Edythe Broad Center of Regenerative Medicine and Stem Cell Research at UCLA and a senior author of the new paper, published today in the journal Nature Medicine. This means the cells are perfectly matched to the patient and it should be a much safer transplant, without the risks of rejection.

People with chronic granulomatous disease, or CGD, have a genetic mutation in one of five genes that help white blood cells attack and destroy bacteria and fungus using a burst of chemicals. Without this defensive chemical burst, patients with the disease are much more susceptible to infections than most people. The infections can be severe to life-threatening, including infections of the skin or bone and abscesses in organs such as lungs, liver or brain. The most common form of CGD is a subtype called X-CGD, which affects only males and is caused by a mutation in a gene found on the X-chromosome.

Other than treating infections as they occur and taking rotating courses of preventive antibiotics, the only treatment option for people with CGD is to receive a bone marrow transplant from a healthy matched donor. Bone marrow contains stem cells called hematopoietic, or blood-forming, stem cells, which produce white blood cells. Bone marrow from a healthy donor can produce functioning white blood cells that effectively ward off infection. But it can be difficult to identify a healthy matched bone marrow donor and the recovery from the transplant can have complications such as graft versus host disease, and risks of infection and transplant rejection.

Patients can certainly get better with these bone marrow transplants, but it requires finding a matched donor and even with a match, there are risks, Kohn said. Patients must take anti-rejection drugs for six to 12 months so that their bodies dont attack the foreign bone marrow.

In the new approach, Kohn teamed up with collaborators at the United Kingdoms National Health Service, France-based Genethon, the U.S. National Institute of Allergy and Infectious Diseases at the National Institutes of Health, and Boston Childrens Hospital. The researchers removed hematopoietic stem cells from X-CGD patients and modified the cells in the laboratory to correct the genetic mutation. Then, the patients own genetically modified stem cells now healthy and able to produce white blood cells that can make the immune-boosting burst of chemicals were transplanted back into their own bodies. While the approach is new in X-CGD, Kohn previously pioneered a similar stem cell gene therapy to effectively cure a form of severe combined immune deficiency (also known as bubble baby disease) in more than 50 babies.

The viral delivery system for the X-CGD gene therapy was developed and fine-tuned by Professor Adrian Thrashers team at Great Ormond Street Hospital, or GOSH, in London, who collaborated with Kohn. The patients ranged in age from 2 to 27 years old; four were treated at GOSH and five were treated in the U.S., including one patient at UCLA Health.

Two people in the new study died within three months of receiving the treatment due to severe infections that they had already been battling before gene therapy. The seven surviving patients were followed for 12 to 36 months after receiving the stem cell gene therapy. All remained free of new CGD-related infections, and six of the seven have been able to discontinue their usual preventive antibiotics.

None of the patients had complications that you might normally see from donor cells and the results were as good as youd get from a donor transplant or better, Kohn said.

An additional four patients have been treated since the new paper was written; all are currently free of new CGD-related infections and no complications have arisen.

Orchard Therapeutics, a biotechnology company of which Kohn is a scientific co-founder, acquired the rights to the X-CGD investigational gene therapy from Genethon. Orchard will work with regulators in the U.S. and Europe to carry out a larger clinical trial to further study this innovative treatment. The aim is to apply for regulatory approval to make the treatment commercially available, Kohn said.

Kohn and his colleagues plan to develop similar treatments for the other forms of CGD caused by four other genetic mutations that affect the same immune function as X-CGD.

Beyond CGD, there are also other diseases caused by proteins missing in white blood cells that could be treated in similar ways, Kohn said.

The research was supported by grants from the California Institute for Regenerative Medicine; the National Heart, Lung and Blood Institute and the National Institute of Allergy and Infectious Diseases, both at the National Institutes of Health; the Wellcome Trust; Boston Childrens Hospital; the National Institute for Health Research Great Ormond Street Hospital Biomedical Research Centre; the Institute for Health Research Biomedical Research Centre at University College London Hospitals NHS Foundation Trust and University College London; the Great Ormond Street Hospital Childrens Charity; the AFM-Tlthon, French Muscular Dystrophy Association; and the European Commission through the Net4CGDconsortium.

See the rest here:
Six patients with rare blood disease are doing well after gene therapy clinical trial - Mirage News

To Read More: Six patients with rare blood disease are doing well after gene therapy clinical trial – Mirage News
categoriaBone Marrow Stem Cells commentoComments Off on Six patients with rare blood disease are doing well after gene therapy clinical trial – Mirage News | dataJanuary 27th, 2020
Read All

Qatar- HMC to introduce regenerative therapy to treat foot and ankle illnesses – MENAFN.COM

By daniellenierenberg

(MENAFN - Gulf Times) The Foot and Ankle sub-specialty at Hamad General Hospital (HGH), part of Hamad Medical Corporation (HMC), will soon introduce the latest medical procedure, BMAC, to treat various illnesses related to foot and ankle.'Bone marrow aspirate concentrate (BMAC) is a regenerative therapy procedure that uses stem cells from a patient's bone marrow to initiate healing for a number of orthopaedic conditions, such as tendinopathy, osteoarthritis and cartilage injuries, said Dr Mohamed Maged Mekhaimar, senior consultant and orthopaedic surgeon at HGH.'This will help treating patients with tendon inflation. It can also be used to treat inflammation on the bottom of the foot as well as for traumatic conditions of the ankle. These services will soon be available at Hamad General Hospital, explained Dr Mekhaimar.Foot and ankle services were started at HGH in 2012. 'Now, there is a great demand for these services in the country as more and more people are approaching us for various issues. The centre provides treatment for several problems such as flat foot problems, among other issues. We also provide treatment for diabetic foot people, he continued.The centre currently performs about five surgeries per day and takes care for all different injuries, including sport injuries.According to the official, the centre also makes use of PRP (Platelet Rich Plasma) machine by which blood is taken from people and then separated. 'Using the PRP machine, we can inject the blood particles to the joints. This facility is available in HGH and the Bone and Joint Center, part of HMC, he noted.'Our clinics are at the Bone and Joint Center. All our patients come through the Bone and Joint Center. We are also in the process of introducing the weight-bearing CT scan machine. With this, we can scan the foot and ankle of the patient while he or she is standing on it. This can give better impression of the condition of the patients, he highlighted.'Some deformity can be better measured through this CT scan machine. It will also be used for treating the knee joint as it is one of the most advanced treatment options available now, he added.

MENAFN2501202000670000ID1099602239

Go here to read the rest:
Qatar- HMC to introduce regenerative therapy to treat foot and ankle illnesses - MENAFN.COM

To Read More: Qatar- HMC to introduce regenerative therapy to treat foot and ankle illnesses – MENAFN.COM
categoriaBone Marrow Stem Cells commentoComments Off on Qatar- HMC to introduce regenerative therapy to treat foot and ankle illnesses – MENAFN.COM | dataJanuary 26th, 2020
Read All

If youre troubled by ache within the nerves, comply with the following tips, know – Sahiwal Tv

By daniellenierenberg

Many folks all over the world will be seen troubled by ache within the veins. And many occasions, even after an excessive amount of therapy, this ache shouldnt be relieved. But within the coming days youll be able to do away with neuralgia utterly, that too with none unwanted side effects. Researchers on the University of Sydney have used human stem cells for excessive ache reduction in mice. Now, theyre shifting in the direction of human trials.

Greg Nelly, senior researcher on the Charles Perkins Center, stated that at occasions, extreme stress on the nerves causes them to get broken. For instance, carpal tunnel syndrome is the median nerve within the fingers ( median nerve ) Due to extreme stress.

->As youll be able to think about, nerve accidents can result in insufferable neuropathic ache. There can also be no efficient therapy to alleviate ache in most sufferers.

Therefore, Nelly and colleagues on the University of Sydney developed an efficient remedy. Researchers have been in a position to create pain-relieving neurons utilizing human stem cells.

Nelly stated that this success implies that for some sufferers affected by nerve ache, we are able to carry out pain-relieving implants from our cells, which might cease the ache.

In the research, researchers collected stem cells from grownup blood samples. Then, used human-induced pluripotent stem cells (iPSCs) from the bone marrow to create pain-relieving cells within the laboratory.

To check the efficacy of the therapy, the group injected neurons that abolished spinal ache in mice affected by extreme neuropathic ache. It was revealed that this therapy supplied full reduction from ache to the mice with none unwanted side effects.

Co-senior creator Dr. Leslie Caron stated that because of this transplant remedy is prone to be an efficient and long-lasting therapy for neuropathic ache.

After shut therapy in mice, the University of Sydney group is shifting ahead for extra intensive research in pigs. Within the following 5 years, theyll check people who are suffering from power ache.

Researchers stated {that a} move check in people will probably be a giant success. This could point out the event of latest non-opioid, non-addictive ache administration methods for sufferers.

More:
If youre troubled by ache within the nerves, comply with the following tips, know - Sahiwal Tv

To Read More: If youre troubled by ache within the nerves, comply with the following tips, know – Sahiwal Tv
categoriaBone Marrow Stem Cells commentoComments Off on If youre troubled by ache within the nerves, comply with the following tips, know – Sahiwal Tv | dataJanuary 26th, 2020
Read All

Watch | Stem cell banking and its benefits – The Hindu

By daniellenierenberg

The blood collected from the umbilical cord of the newborn is a rich source of stem cells. This blood is collected and sent to a cord blood bank, where the stem cells are separated, tested, processed, and preserved in liquid nitrogen. Technically, there is no expiry date and these stem cells can be preserved for a lifetime. Scientifically, evidence exists that they can be stored for about 20 years. The stem cells can treat around 70 blood related disorders and genetic disorders including thalassemia, sickle cell anaemia, leukaemia, and immune related disorders.

Stem cells taken from umbilical cord blood are like those taken from bone marrow, capable of producing all blood cells: red cells, platelets and immune system cells. When used, stem cells are first concentrated, then injected into the patient. Once transfused, they produce new cells of every kind.

They're capable of producing all types of blood cells: red cells, platelets and immune system cells. The stem cells can treat around 80 blood related illnesses like leukaemia, lymphomas, several genetic conditions and immune related disorders. But given the present state of medicine, they are effective only for around a dozen of them

See the article here:
Watch | Stem cell banking and its benefits - The Hindu

To Read More: Watch | Stem cell banking and its benefits – The Hindu
categoriaBone Marrow Stem Cells commentoComments Off on Watch | Stem cell banking and its benefits – The Hindu | dataJanuary 25th, 2020
Read All

Europe’s guardian of stem cells and hopes, real and unrealistic – Yahoo News

By daniellenierenberg

Poland has emerged as Europe's leader in stem cell storage, a billion-dollar global industry that is a key part of a therapy that can treat leukaemias but raises excessive hopes.

Submerged in liquid nitrogen vapour at a temperature of minus 175 degrees Celsius, hundreds of thousands of stem cells from all over Europe bide their time in large steel barrels on the outskirts of Warsaw.

Present in blood drawn from the umbilical cord of a newborn baby, stem cells can help cure serious blood-related illnesses like leukaemias and lymphomas, as well as genetic conditions and immune system deficits.

Polish umbilical cord blood bank PBKM/FamiCord became the industry's leader in Europe after Swiss firm Cryo-Save went bankrupt early last year.

It is also the fifth largest in the world, according to its management, after two companies in the United States, a Chinese firm and one based in Singapore.

Since the first cord blood transplant was performed in France in 1988, the sector has significantly progressed, fuelling hopes.

- Health insurance -

Mum-of-two Teresa Przeborowska has firsthand experience.

At five years old, her son Michal was diagnosed with lymphoblastic leukaemia and needed a bone marrow transplant, the entrepreneur from northern Poland said.

The most compatible donor was his younger sister, Magdalena.

When she was born, her parents had a bag of her cord blood stored at PBKM.

More than three years later, doctors injected his sister's stem cells into Michal's bloodstream.

It was not quite enough for Michal's needs but nicely supplemented harvested bone marrow.

As a result, Michal, who is nine, "is now flourishing, both intellectually and physically," his mum told AFP.

A cord blood transplant has become an alternative to a bone marrow transplant when there is no donor available, with a lower risk of complications.

Stem cells taken from umbilical cord blood are like those taken from bone marrow, capable of producing all blood cells: red cells, platelets and immune system cells.

Story continues

When used, stem cells are first concentrated, then injected into the patient. Once transfused, they produce new cells of every kind.

At the PBKM laboratory, "each container holds up to 10,000 blood bags... Safe and secure, they wait to be used in the future," its head, Krzysztof Machaj, said.

The bank holds around 440,000 samples, not including those from Cryo-Save, he said.

If the need arises, the "blood will be ready to use without the whole process of looking for a compatible donor and running blood tests," the biologist told AFP.

For families who have paid an initial nearly 600 euros ($675) and then an annual 120 euros to have the blood taken from their newborns' umbilical cords preserved for around 20 years, it is a kind of health insurance promising faster and more effective treatment if illness strikes.

But researchers also warn against unrealistic expectations.

- Beauty products -

Haematologist Wieslaw Jedrzejczak, a bone marrow pioneer in Poland, describes promoters of the treatment as "sellers of hope", who "make promises that are either impossible to realise in the near future or downright impossible to realise at all for biological reasons."

He compares them to makers of beauty products who "swear their cream will rejuvenate the client by 20 years."

Various research is being done on the possibility of using the stem cells to treat other diseases, notably nervous disorders. But the EuroStemCell scientist network warns that the research is not yet conclusive.

"There is a list of almost 80 diseases for which stem cells could prove beneficial," US haematologist Roger Mrowiec, who heads the clinical laboratory of the cord blood programme Vitalant in New Jersey, told AFP.

"But given the present state of medicine, they are effective only for around a dozen of them, like leukaemia or cerebral palsy," he said.

"It's not true, as it's written sometimes, that we can already use them to fight Parkinson's disease or Alzheimer's disease or diabetes."

EuroStemCell also cautions against private blood banks that "advertise services to parents suggesting they should pay to freeze their child's cord blood... in case it's needed later in life."

"Studies show it is highly unlikely that the cord blood will ever be used for their child," the network said.

It also pointed out that there could be a risk of the child's cells not being useable anyway without reintroducing the same illness.

Some countries, such as Belgium and France, are cautious and ban the storage of cord blood for private purposes. Most EU countries however permit it while imposing strict controls.

- Rapid growth -

In the early 2000s, Swiss company Cryo-Save enjoyed rapid growth.

Greeks, Hungarians, Italians, Spaniards and Swiss stored blood from their newborns with the company for 20 years on payment of 2,500 euros upfront.

When the firm was forced to close in early 2019, clients were left wondering where their stem cells would end up.

Under a kind of back-up agreement, the samples of some 250,000 European families were transferred for storage at PBKM.

The Polish firm, founded in 2002 with two million zlotys (around 450,000 euros, $525,000), has also grown quickly.

Present under the FamiCord brand in several countries, PBKM has some 35 percent of the European market, excluding Cryo-Save assets.

Over the last 15 months, outside investors have contributed 63 million euros to the firm, PBKM's chief executive Jakub Baran told AFP.

But the company has not escaped controversy: the Polityka weekly recently published a critical investigative report on several private clinics that offer what was described as expensive treatment involving stem cells held by PBKM.

Read the original here:
Europe's guardian of stem cells and hopes, real and unrealistic - Yahoo News

To Read More: Europe’s guardian of stem cells and hopes, real and unrealistic – Yahoo News
categoriaBone Marrow Stem Cells commentoComments Off on Europe’s guardian of stem cells and hopes, real and unrealistic – Yahoo News | dataJanuary 25th, 2020
Read All

UAB scientist studies aging through gray hair, says hair could be rejuvenated – AL.com

By daniellenierenberg

Gray hair got you down? Scientists may have a cure for that.

Okay, maybe not a cure. But, more information about why youre going gray, and what can be done about it.

Dr. Melissa Harris, an assistant professor at the University of Alabama at Birminghams Department of Biology, has spent the last ten years studying melanocyte stem cells and what happens when they fail.

Harris runs a molecular biology lab at UAB and uses CRISPR gene editing tools, single-cell sequencing studies, and network analysis algorithms. She uses gray hair as a model for aging, because she doesnt always need a microscopeshe can see the state of your melanocyte stem cells right away. If hair is all one color, Harris said, the melanocyte stem cells are healthy; but if there are grays mixed in, something isnt right.

Gray hair isnt always an inevitable part of aging, the university said. Through Harris research, shes learned that age isnt the only reason these cells fail, and now Harris is working with gray-haired mice to show there could be a way to bring the cells- and hair pigments- back to life. Shes doing that by working with a biotech startup to study an experimental compound that appears to restore hair color long-term in those mice.

Harris work applies to autoimmune diseases and to melanoma, but she said her primary goal is to understand why somatic stem cells (those found in muscles, bones, and organs that are responsible for tissue regeneration, immune defense, hair color and more) start to fail as a person ages. Most of those stem cell populations are hard to work with in the lab, Harris said, but melanocyte stem cells are an exception.

Does hair graying cause you to die? Harris said. No, you can watch melanocyte stem cells from birth to the end. But, she added that the same cant be said for cells like hematopoetic stem cells, which pump red blood cells in bone marrow. You cant live long without them, Harris said.

Her research will reveal more about the bodys aging process and the life cycles of those stem cells.

Harris is often known as the gray-hair lady in the lab, but she stresses that her gray hair research has bigger implications. Everyone gets gray hair It is considered a vanity science, she said. I am not an abnormally vain person My lab has picked the model that is the most appropriate method to investigate what happens to stem cells as we age.

The work has earned her a grant from the NIHs National Institute of Aging. A paper published by her lab in 2018 showed that MITF, a certain protein that is the master regulator turning on pigmentation genes also represses the innate immune system, according to UAB. The university said when Harris worked with the MITF-deficient mice with a virus, the melanocyte stem cells suffered and the mice got gray hair. The study was globally recognized, and featured in several publications.

Perhaps, in an individual who is healthy yet predisposed for gray hair, because they produce less MITF, getting an everyday viral infection is just enough to cause the decline of their melanocytes and melanocyte stem cells, leading to premature gray hair, Harris told UAB News.

Harris started working with the biotech startup when she was contacted by them last year. They were developing an experimental compound that would regrow hair, and they wanted to know if she would test it on her mice. Harris said she was skeptical, but she conducted a small trial.

It worked. Harris said when she tests gray-haired mice with the compound, she sees hair color come back.

Some gray hairs could be rejuvenated, the university said, through compounds to stimulate the cells. (Courtesy, UAB)

And we can take these same mice, pluck the hair and when new hairs grow out they retain the higher level of pigmentation, suggesting this is permanent, she said. This compound is reprogramming the stem cells, taking them to a younger state, allowing them to start up again.

Harris and Joseph Palmer, one of her doctoral students, are also studying a theory that the melanocyte stem cells spend most of their time in a dormant state, and that the cells can possibly be stimulated.

(Spanish doctors in a study) suggested that some melanocyte stem cells are retained in gray hairs, Harris said. We thought that once you go gray the stem cells are all lost theres no going back. But presumably they can be reactivated. That study means, according to Harris, there may be therapies to reactive the cells, and the compound shes working with alongside the startup could be a promising way forward, according to UAB.

We have an opportunity with this company to find out what are the potential ways we can fix a broken system, Harris said. Were always looking at whats broken and rarely do we get to go in the other direction, towards tissue rejuvenation. So this is exciting.

Read this article:
UAB scientist studies aging through gray hair, says hair could be rejuvenated - AL.com

To Read More: UAB scientist studies aging through gray hair, says hair could be rejuvenated – AL.com
categoriaBone Marrow Stem Cells commentoComments Off on UAB scientist studies aging through gray hair, says hair could be rejuvenated – AL.com | dataJanuary 25th, 2020
Read All

Get rid of the ache within the nerves discovered with the following pointers, learn – Sahiwal Tv

By daniellenierenberg

Many folks around the globe will be seen troubled by ache within the veins. And many occasions, even after an excessive amount of therapy, this ache just isnt relieved. But within the coming days you possibly can do away with neuralgia fully, that too with none unwanted effects. Researchers on the University of Sydney have used human stem cells for excessive ache aid in mice.

->Now, theyre shifting in direction of human trials.

Greg Nelly, senior researcher on the Charles Perkins Center, stated that at occasions, extreme strain on the nerves causes them to get broken. For instance, carpal tunnel syndrome is the median nerve within the arms ( median nerve ) Due to extreme strain. As you possibly can think about, nerve accidents can result in insufferable neuropathic ache. There can also be no efficient therapy to alleviate ache in most sufferers.

Therefore, Nelly and colleagues on the University of Sydney developed an efficient remedy. Researchers have been capable of create pain-relieving neurons utilizing human stem cells.

Nelly stated that this success implies that for some sufferers affected by nerve ache, we are able to carry out pain-relieving implants from our cells, which might cease the ache.

In the examine, researchers collected stem cells from grownup blood samples. Then, used human-induced pluripotent stem cells (iPSCs) from the bone marrow to create pain-relieving cells within the laboratory.

To check the efficacy of the therapy, the staff injected neurons that abolished spinal ache in mice affected by extreme neuropathic ache. It was revealed that this therapy supplied full aid from ache to the mice with none unwanted effects.

Co-senior creator Dr. Leslie Caron stated that which means that transplant remedy is more likely to be an efficient and long-lasting therapy for neuropathic ache.

After shut therapy in mice, the University of Sydney staff is shifting ahead for extra in depth research in pigs. Within the subsequent 5 years, theyll check people that suffer from power ache.

Researchers stated {that a} move check in people can be an enormous success. This might point out the event of latest non-opioid, non-addictive ache administration methods for sufferers.

Visit link:
Get rid of the ache within the nerves discovered with the following pointers, learn - Sahiwal Tv

To Read More: Get rid of the ache within the nerves discovered with the following pointers, learn – Sahiwal Tv
categoriaBone Marrow Stem Cells commentoComments Off on Get rid of the ache within the nerves discovered with the following pointers, learn – Sahiwal Tv | dataJanuary 25th, 2020
Read All

Pain treatment using human stem cells a success – News – The University of Sydney

By daniellenierenberg

Chronic pain cost an estimated $139.3 billion in 2018. Image: iStock, Top image: Pexels

Researchers at the University of Sydney have used human stem cells to make pain-killing neurons that provide lasting relief in mice, without side effects, in a single treatment. The next step is to perform extensive safety tests in rodents and pigs, and then move to human patients suffering chronic pain within the next five years.

If the tests are successful in humans, it could be a major breakthrough in the development of new non-opioid, non-addictive pain management strategies for patients, the researchers said.

Thanks to funding from the NSW Ministry of Health, we are already moving towards testing in humans, said Associate Professor Greg Neely, a leader in pain research at the Charles Perkins Centre and the School of Life and Environmental Sciences.

Nerve injury can lead to devastating neuropathic pain and for the majority of patients there are no effective therapies. This breakthrough means for some of these patients, we could make pain-killing transplants from their own cells, and the cells can then reverse the underlying cause of pain.

Go here to see the original:
Pain treatment using human stem cells a success - News - The University of Sydney

To Read More: Pain treatment using human stem cells a success – News – The University of Sydney
categoriaBone Marrow Stem Cells commentoComments Off on Pain treatment using human stem cells a success – News – The University of Sydney | dataJanuary 24th, 2020
Read All

Europe’s guardian of stem cells and hopes, real and unrealistic – Deccan Herald

By daniellenierenberg

Poland has emerged as Europe's leader in stem cell storage, a billion-dollar global industry that is a key part of a therapy that can treat leukaemias but raises excessive hopes.

Submerged in liquid nitrogen vapour at a temperature of minus 175 degrees Celsius, hundreds of thousands of stem cells from all over Europe bide their time in large steel barrels on the outskirts of Warsaw.

Present in blood drawn from the umbilical cord of a newborn baby, stem cells can help cure serious blood-related illnesses like leukaemias and lymphomas, as well as genetic conditions and immune system deficits.

Polish umbilical cord blood bank PBKM/FamiCord became the industry's leader in Europe after Swiss firm Cryo-Save went bankrupt early last year.

It is also the fifth-largest in the world, according to its management, after two companies in the United States, a Chinese firm and one based in Singapore.

Since the first cord blood transplant was performed in France in 1988, the sector has significantly progressed, fuelling hopes.

Mum-of-two Teresa Przeborowska has firsthand experience.

At five years old, her son Michal was diagnosed with lymphoblastic leukaemia and needed a bone marrow transplant, the entrepreneur from northern Poland said.

The most compatible donor was his younger sister, Magdalena.

When she was born, her parents had a bag of her cord blood stored at PBKM.

More than three years later, doctors injected his sister's stem cells into Michal's bloodstream.

It was not quite enough for Michal's needs but nicely supplemented harvested bone marrow.

As a result, Michal, who is nine, "is now flourishing, both intellectually and physically," his mum told AFP.

A cord blood transplant has become an alternative to a bone marrow transplant when there is no donor available, with a lower risk of complications.

Stem cells taken from umbilical cord blood are like those taken from bone marrow, capable of producing all blood cells: red cells, platelets and immune system cells.

When used, stem cells are first concentrated, then injected into the patient. Once transfused, they produce new cells of every kind.

At the PBKM laboratory, "each container holds up to 10,000 blood bags... Safe and secure, they wait to be used in the future," its head, Krzysztof Machaj, said.

The bank holds around 440,000 samples, not including those from Cryo-Save, he said.

If the need arises, the "blood will be ready to use without the whole process of looking for a compatible donor and running blood tests," the biologist told AFP.

For families who have paid an initial nearly 600 euros ($675) and then an annual 120 euros to have the blood taken from their newborns' umbilical cords preserved for around 20 years, it is a kind of health insurance promising faster and more effective treatment if illness strikes.

But researchers also warn against unrealistic expectations.

Haematologist Wieslaw Jedrzejczak, a bone marrow pioneer in Poland, describes promoters of the treatment as "sellers of hope", who "make promises that are either impossible to realise in the near future or downright impossible to realise at all for biological reasons."

He compares them to makers of beauty products who "swear their cream will rejuvenate the client by 20 years."

Various research is being done on the possibility of using the stem cells to treat other diseases, notably nervous disorders. But the EuroStemCell scientist network warns that the research is not yet conclusive.

"There is a list of almost 80 diseases for which stem cells could prove beneficial," US haematologist Roger Mrowiec, who heads the clinical laboratory of the cord blood programme Vitalant in New Jersey, told AFP.

"But given the present state of medicine, they are effective only for around a dozen of them, like leukaemia or cerebral palsy," he said.

"It's not true, as it's written sometimes, that we can already use them to fight Parkinson's disease or Alzheimer's disease or diabetes."

EuroStemCell also cautions against private blood banks that "advertise services to parents suggesting they should pay to freeze their child's cord blood... in case it's needed later in life."

"Studies show it is highly unlikely that the cord blood will ever be used for their child," the network said.

It also pointed out that there could be a risk of the child's cells not being useable anyway without reintroducing the same illness.

Some countries, such as Belgium and France, are cautious and ban the storage of cord blood for private purposes. Most EU countries, however, permit it while imposing strict controls.

In the early 2000s, Swiss company Cryo-Save enjoyed rapid growth.

Greeks, Hungarians, Italians, Spaniards and Swiss stored blood from their newborns with the company for 20 years on payment of 2,500 euros upfront.

When the firm was forced to close in early 2019, clients were left wondering where their stem cells would end up.

Under a kind of back-up agreement, the samples of some 250,000 European families were transferred for storage at PBKM.

The Polish firm, founded in 2002 with two million zlotys (around 450,000 euros, $525,000), has also grown quickly.

Present under the FamiCord brand in several countries, PBKM has some 35 per cent of the European market, excluding Cryo-Save assets.

Over the last 15 months, outside investors have contributed 63 million euros to the firm, PBKM's chief executive Jakub Baran told AFP.

But the company has not escaped controversy: the Polityka weekly recently published a critical investigative report on several private clinics that offer what was described as expensive treatment involving stem cells held by PBKM.

More here:
Europe's guardian of stem cells and hopes, real and unrealistic - Deccan Herald

To Read More: Europe’s guardian of stem cells and hopes, real and unrealistic – Deccan Herald
categoriaBone Marrow Stem Cells commentoComments Off on Europe’s guardian of stem cells and hopes, real and unrealistic – Deccan Herald | dataJanuary 24th, 2020
Read All

Blood drive to honor Franklin child with cancer – Daily Journal

By daniellenierenberg

The tiny body seemed consumed by tubes and wires and monitors.

Just one day prior, Stephanie and Cody Smith had learned the terrible truth about why their 18-month-old son, Charlie, had been so sick recently. He had neuroblastoma, a cancer that forms on the nerve endings. Scans revealed cancer was on his kidney, lungs, bone and lymph nodes.

To stem the aggressive cancer, his doctors immediately got to work, putting in catheters, taking bone marrow biopsies and preparing for the start of intense chemotherapy. Charlie lay in his hospital bed eating Cheetos Puffs, his favorite food, and sitting with his parents.

"It was hard when we got the news," Stephanie Smith said. "I tried to be calm and collected; I had to be strong for my baby. But its been hard."

Story continues below gallery

The past two months have come straight out of a nightmare for the Smith family. Since Charlie was diagnosed with Stage IV neuroblastoma in November, each day brings uncertainty.

The Franklin family has spent 49 of the last 60 days at Riley Hospital for Children at IU Health. Charlie has gone through rounds of chemotherapy, suffering through fevers, mouth sores, extreme fatigue and nausea that wracked his small body. His treatment will last over the next 18 months, and will include chemotherapy, stem cell transplants, blood transfusions, radiation and immunotherapy.

But despite everything theyve been through, the Smiths remain resolute that Charlie will get better. They have relied on their faith, and an army of supporters who have stepped forward to help them in their worst time, to get them through.

"It was amazing to see so many people come up and love on us. It has taught us to be generous people; weve always thought we were generous people, but when you see the number of people who care for you and pray for you and support you, its really amazing," Stephanie Smith said.

The Smiths have partnered with Versiti Blood Center of Indiana to host a blood drive in Greenwood Saturday. The Cheering for Charlie event will be held from 6 a.m. to 2 p.m., to help increase blood supplies for patients such as Charlie who rely on transfusions to survive.

Every two seconds, someone needs life-saving blood, whether theyre bravely battling disease like Charlie, undergoing surgery or are victims of trauma," said Duane Brodt, spokesman for Versiti. "People need people since blood cant be manufactured."

For most of his life, Charlie was a happy-go-lucky toddler. He loved to smile and laugh, beaming joy. Where his 3-year-old brother Henry was more of a wild child, Stephanie Smith said, Charlie seemed to always be in a pleasant, good mood.

His parents described him as their "happy baby."

Thats what made his lethargy, lack of appetite and gradual decline in health so concerning.

"He was learning how to walk over the summer, and started getting sick," Stephanie Smith said. "We just thought it was a virus; we didnt think of the worst."

Charlie developed a low-grade fever, wasnt eating well and was falling asleep unexpectedly while playing with toys. He wasnt acting like himself, Stephanie Smith said.

During a visit to his pediatrician, the doctor found a hard area on Charlies abdomen, and recommended doing some blood tests and taking an X-ray. Those tests only led to more questions he had severe range anemia and elevated levels of platelets in his blood. But the doctor didnt have any conclusive answers as to what was causing it.

Stephanie Smith, a nurse at Franciscan Health, started hearing warning bells in her mind. That, combined with a mothers intuition, convinced her that they needed to take Charlie to Riley Hospital for Children. After 12 hours in the emergency room, and dozens of tests, doctors found a large tumor in Charlies abdomen.

"Sometimes, when kids are diagnosed with cancer, they can go home and be in and out of the hospital for treatment, but Charlie was really sick. The tumor was pushing on his kidney, damaging his kidney, so we had to stay in the hospital," Stephanie Smith said.

The pathology lab at Riley Hospital for Children confirmed the tumor was neuroblastoma. The cancer forms in immature nerve endings, often in the adrenal glands located near the kidneys and is most common in children age 5 and under, according to the American Cancer Society.

But the cancer is very rare; only about 800 new cases are diagnosed in the U.S. each year, according to the American Cancer Society.

Neuroblastomas grow and spread very rapidly, so treatment would have to be aggressive, doctors explained to the family. Charlies oncologist recommended starting with two rounds of focused chemotherapy, followed by the extraction of his red blood cells for stem cell transplants, then another three rounds of chemotherapy.

Two different stem cell transplants would be held about a month apart, and Charlie would start radiation treatment. Immunotherapy, which jolts the immune system into targeting and killing cancer cells, would be the final part of the regimen.

Almost immediately, Charlie started his chemotherapy.

"It grows so quickly, that we had to be aggressive. The beginning was pretty intense," Stephanie Smith said.

The treatment was hard on Charlies young body. He developed mouth sores and didnt want to eat, and his nausea left him miserable. The Smith family essentially relocated to the hospital, staying with him constantly.

But at the same time, their friends and family, as well as complete strangers, stepped up to offer help. A meal train was set up to provide the family with food, and prayers came from all directions.

A GoFundMe page has raised more than $36,000 for the family. A community Facebook page has more than 5,000 members.

"We had a rally of people come around us," Stephanie Smith said. "We couldnt have done it without all of the people who have come together."

Charlie has completed his first four rounds of chemotherapy, and on Jan. 20, he was able to return home with his family to wait for surgery to remove the tumor in his abdomen. That operation is tentatively going to be early to mid February.

In the meantime, the family has been soaking in the opportunity to be together somewhere besides the hospital. They have also been working to plan the blood drive being held on Saturday.

Charlie has relied on blood transfusions throughout his treatment, and a blood drive would be a way to raise awareness of the importance of those transfusions to cancer patients, Stephanie Smith said.

"Charlie received quite a few blood products, especially early on in his treatment. He had 12 transfusions in these 2 1/2 months. For his little body, thats a lot," she said. "Being a nurse, I didnt realize the number of cancer patients who need blood products. Its so important. So this was a way to let people know that."

Stephanie Smiths sister, Shelby Richards, knew people who had organized drives with their friends and helped the family get the Cheering for Charlie drive going.

The drive is a perfect opportunity to remind people that blood donations are vitally important, Brodt said. Versiti Blood Center of Indiana needs to collect at least 560 blood donations every day to support the need at its 80 hospital partners throughout the state, he said.

"So our Cheering for Charlie will truly make a difference and help save lives," Brodt said.

For the Smith family, the drive is a way to give back for all the love theyve been shown.

"Its really cool for us to see how many people have signed up, and also be advocates for other people who need blood, to just get the word out there about how important it is," Stephanie Smith said. "Its encouraging for us to see people come out to support Charlie and kids like him."

If you go

Cheering for Charlie blood drive

What: A blood drive honoring Charlie Smith, an 18-month-old Franklin child diagnosed with neuroblastoma, a cancer of the nerve cells.

When: 6 a.m. to 2 p.m. Saturday

Where: Versiti Blood Center of Indiana, 8739 U.S. 31 S., Indianapolis

Who can donate: Generally, anyone in good health age 16 and up can donate. Make sure you do not have a cold, flu or sore throat at the time of donation.

How to schedule an appointment: Go to Versiti.org/Indiana

Information: Learn more about Charlie on the Cheering for Charlie! Facebook group page.

Excerpt from:
Blood drive to honor Franklin child with cancer - Daily Journal

To Read More: Blood drive to honor Franklin child with cancer – Daily Journal
categoriaBone Marrow Stem Cells commentoComments Off on Blood drive to honor Franklin child with cancer – Daily Journal | dataJanuary 24th, 2020
Read All

Advancells Group & IFC Concluded their 3-Day Workshop on Regenerative Medicine – MENAFN.COM

By daniellenierenberg

(MENAFN - ForPressRelease) 11

New Delhi 23rd January 2020 On Saturday, January 18th, 2020, the Advancells Group & the International Fertility Center together ended their first workshop Sub-Specialty Training in Application of Regenerative Medicine (S.T.A.R. 2020). The three-day workshop had specialized doctors, medical practitioners, learned scientists of Advancells, the leaders in cell manufacturing & processes and IFC, one of India's most prestigious Fertility institute who were joined by candidates with MBBS/BAMS/BHMS/BPharma & Master's degree in Life Sciences.

The key-note speaker of the workshop was Dr. Rita Bakshi, founder and chairperson of International Fertility Centre, the oldest fertility clinic and one of the most renowned IVF clinics in India, one of the organizers of the event. Participants also had a privilege to listen to Dr. Sachin Kadam, CTO, Advancells and gain hands-on experience in the preparation of PRP; Liposuction method; and Bone Marrow aspiration. All these techniques were talked about at length and demonstrated in the form of manual & kit-based models to help the candidates gain exposure.

Dr. Punit Prabha, Head of Clinical Research and Dr. Shradha Singh Gautam, Head of Lab Operations at Advancells successfully set the base of stem cell biology for the participants who were experts in gynecology field, stem cell research and pain specialist. With the help of detailed analysis of 'Application of PRP for Skin rejuvenation'; 'Preparation of Micro-fragmented Adipose Tissue and Nano Fat & SVF (Stromal Vascular Fraction) from Adipose Tissue'; and 'Cell Culturing and Expansion in a Laboratory', applicants understood the application of stem cells in aesthetics, cosmetology, and anti-aging.

Vipul Jain, Founder & CEO of Advancells Group said, 'Educating young scientists about stem cells is important for us. With this workshop we wanted to discuss and share the challenges and lessons we have learned in our journey of curing our customers. We wanted to establish more concrete knowledge base in the presence of subject matter experts and help our attendees in more possible ways. We are hopeful to have successfully achieved what we claimed with this workshop'.

Given the resounding success of the Sub-Specialty Training in Application of Regenerative Medicine (S.T.A.R. 2020), it's hoped that the future events shall offer even greater wisdom to the participants by helping them improve and the lead the community into the age of greater awareness.

Advancells Group Advancells is leading the field of stem cell therapies in India and abroad, with representative offices in Bangladesh and Australia. The company provides arrangements for stem cell banking and protocols for partner doctors and hospitals which they can use for treating the patients using regenerative medicine. With a GMP compliant research and processing center that works on different cell lines from various sources such as Bone Marrow, Adipose Tissue, Dental Pulp, Blood, Cord Tissue etc. Advancells also intends to file a patent for this processing technology soon.

User :- Ajit Singh

Email :

Mobile:- 9953809503

MENAFN2401202000703206ID1099596615

Read the original:
Advancells Group & IFC Concluded their 3-Day Workshop on Regenerative Medicine - MENAFN.COM

To Read More: Advancells Group & IFC Concluded their 3-Day Workshop on Regenerative Medicine – MENAFN.COM
categoriaBone Marrow Stem Cells commentoComments Off on Advancells Group & IFC Concluded their 3-Day Workshop on Regenerative Medicine – MENAFN.COM | dataJanuary 24th, 2020
Read All

Advancells Group, IFC concluded their three-day workshop on Regenerative Medicine – ANI News

By daniellenierenberg

ANI | Updated: Jan 23, 2020 17:49 IST

New Delhi [India], Jan 23 (ANI/Business Wire India): On Saturday, January 18 2020, the Advancells Group and the International Fertility Center together ended their first workshop - Sub-Specialty Training in Application of Regenerative Medicine (STAR 2020).The three-day workshop had specialized doctors, medical practitioners, learned scientists of Advancells, the leaders in cell manufacturing and processes and IFC, one of India's most prestigious Fertility institutes who were joined by candidates with MBBS/BAMS/BHMS/BPharma and Master's degree in Life Sciences.The key-note speaker of the workshop was Dr Rita Bakshi, founder and chairperson of International Fertility Centre, the oldest fertility clinic and one of the most renowned IVF clinics in India, one of the organizers of the event.Participants also had a privilege to listen to Dr Sachin Kadam, CTO, Advancells and gain hands-on experience in the preparation of PRP; Liposuction method; and Bone Marrow aspiration. All these techniques were talked about at length and demonstrated in the form of manual and kit-based models to help the candidates gain exposure.Dr Punit Prabha, Head of Clinical Research and Dr Shradha Singh Gautam, Head of Lab Operations at Advancells successfully set the base of stem cell biology for the participants who were experts in gynecology field, stem cell research and pain specialist.With the help of detailed analysis of 'Application of PRP for Skin rejuvenation'; 'Preparation of Micro-fragmented Adipose Tissue and Nano Fat & SVF (Stromal Vascular Fraction) from Adipose Tissue'; and 'Cell Culturing and Expansion in a Laboratory', applicants understood the application of stem cells in aesthetics, cosmetology, and anti-ageing."Educating young scientists about stem cells is important for us. With this workshop, we wanted to discuss and share the challenges and lessons we have learned in our journey of curing our customers," said Vipul Jain, founder and CEO of Advancells Group."We wanted to establish a more concrete knowledge base in the presence of subject matter experts and help our attendees in more possible ways. We are hopeful to have successfully achieved what we claimed with this workshop," he added. Given the resounding success of the Sub-Specialty Training in Application of Regenerative Medicine (STAR 2020), it's hoped that the future events shall offer even greater wisdom to the participants by helping them improve and the lead the community into the age of greater awareness.This story is provided by BusinessWire India. ANI will not be responsible in any way for the content of this article. (ANI/BusinessWire India)

Continued here:
Advancells Group, IFC concluded their three-day workshop on Regenerative Medicine - ANI News

To Read More: Advancells Group, IFC concluded their three-day workshop on Regenerative Medicine – ANI News
categoriaBone Marrow Stem Cells commentoComments Off on Advancells Group, IFC concluded their three-day workshop on Regenerative Medicine – ANI News | dataJanuary 24th, 2020
Read All

Page 65«..1020..64656667..7080..»


Copyright :: 2024