Cord blood donor found for Quebec woman battling leukemia for second time

MONTREALDoctors say they have found an umbilical cord for a Quebec woman who is battling leukemia for a second time.

Mai Duong recently made a desperate online plea for a compatible stem cell donor.

Duong and doctors told a news conference in Montreal on Tuesday the umbilical cord came from a woman who gave birth and decided to donate it.

A donor was found after a global search was undertaken to find either a bone marrow or cord blood stem for a transplant.

A tearful Duong said she will now spend the next six to eight weeks in treatment.

But the 34-year-old Vietnamese-Canadian, who has a 4-year-old daughter, adds she still has to undergo chemotherapy and radiation treatment before the transplant.

Duong successfully fought off acute leukemia in 2013 with chemotherapy. She had to terminate a 15-week pregnancy to undergo the treatment.

Duong was in remission until a blood test revealed leukemia had returned this past May. Finding the right person was a challenge especially for those who are from a non-Caucasian background.

Read more here:
Cord blood donor found for Quebec woman battling leukemia for second time

Quebec leukemia patient Mai Duong finds cord blood donor

A Quebec womans desperate, months-long search for a compatible stem cell or umbilical cord match is over.

Mai Duong, a 34-year-old Vietnamese-Canadian battling acute leukemia, announced Tuesday that she has finally found a match.

"I'm going to have the transplant and hopefully everything will go well and hopefully I'll have a new marrow," Duong tearfully told reporters Tuesday. "I just hope I'm going to beat cancer once and for all."

"A woman gave birth to her child and has donated her baby's umbilical cord to save another life," reads a post on the Save Mai Duong Facebook page. "Thank you dear mommy, we cannot fathom the importance of your gesture. I am very moved."

Duong beat cancer last year, after chemotherapy that she had to terminate a 15-week pregnancy to undergo.

She was in remission until May, when blood tests revealed the leukemia had returned.

"Seventy per cent of people who had that type of leukemia were just cured with chemotherapy and unfortunately I'm in the 30 per cent," she said at the time.

Doctors said Duong would need a bone marrow transplant or cord blood stem cells and she needed it fast. Despite being on the international list, doctors struggled to find a match.

Duong said, for people who aren't Caucasian, finding the right donor can be like searching for a needle-in-a-haystack.

"Less than one per cent of the 25 million donors worldwide are Vietnamese," she wrote on her website. "All ethnic communities are severely under-represented in the world donor bank, making finding a compatible donor very difficult for me and countless others who are currently waiting for a transplant."

Read this article:
Quebec leukemia patient Mai Duong finds cord blood donor

Quebec leukemia patient Mai Duong finds blood cord donor

A Quebec womans desperate, months-long search for a compatible stem cell or umbilical cord match is over.

Mai Duong, a 34-year-old Vietnamese-Canadian battling acute leukemia, announced Tuesday that she has finally found a match.

"I'm going to have the transplant and hopefully everything will go well and hopefully I'll have a new marrow," Duong tearfully told reporters Tuesday. "I just hope I'm going to beat cancer once and for all."

"A woman gave birth to her child and has donated her baby's umbilical cord to save another life," reads a post on the Save Mai Duong Facebook page. "Thank you dear mommy, we cannot fathom the importance of your gesture. I am very moved."

Duong beat cancer last year, after chemotherapy that she had to terminate a 15-week pregnancy to undergo.

She was in remission until May, when blood tests revealed the leukemia had returned.

"Seventy per cent of people who had that type of leukemia were just cured with chemotherapy and unfortunately I'm in the 30 per cent," she said at the time.

Doctors said Duong would need a bone marrow transplant or cord blood stem cells and she needed it fast. Despite being on the international list, doctors struggled to find a match.

Duong said, for people who aren't Caucasian, finding the right donor can be like searching for a needle-in-a-haystack.

"Less than one per cent of the 25 million donors worldwide are Vietnamese," she wrote on her website. "All ethnic communities are severely under-represented in the world donor bank, making finding a compatible donor very difficult for me and countless others who are currently waiting for a transplant."

Excerpt from:
Quebec leukemia patient Mai Duong finds blood cord donor

Quebec leukemia patient Mai Duong finds stem cell donor

A Quebec womans desperate, months-long search for a compatible stem cell or umbilical cord match is over.

Mai Duong, a 34-year-old Vietnamese-Canadian battling acute leukemia, announced Tuesday that she has finally found a match.

"I'm going to have the transplant and hopefully everything will go well and hopefully I'll have a new marrow," Duong tearfully told reporters Tuesday. "I just hope I'm going to beat cancer once and for all."

"A woman gave birth to her child and has donated her baby's umbilical cord to save another life," reads a post on the Save Mai Duong Facebook page. "Thank you dear mommy, we cannot fathom the importance of your gesture. I am very moved."

Duong beat cancer last year, after chemotherapy that she had to terminate a 15-week pregnancy to undergo.

She was in remission until May, when blood tests revealed the leukemia had returned.

"Seventy per cent of people who had that type of leukemia were just cured with chemotherapy and unfortunately I'm in the 30 per cent," she said at the time.

Doctors said Duong would need a bone marrow transplant or cord blood stem cells and she needed it fast. Despite being on the international list, doctors struggled to find a match.

Duong said, for people who aren't Caucasian, finding the right donor can be like searching for a needle-in-a-haystack.

"Less than one per cent of the 25 million donors worldwide are Vietnamese," she wrote on her website. "All ethnic communities are severely under-represented in the world donor bank, making finding a compatible donor very difficult for me and countless others who are currently waiting for a transplant."

Excerpt from:
Quebec leukemia patient Mai Duong finds stem cell donor

Stem Cell Research – The UT Health Science Center at …

From trying to create new cartilage in the laboratory to clinical trials for patients with brain injuries, scientists and physicians at The University of Texas Health Science Center at Houston (UTHealth) are leading the way in stem cell research.

In partnership with Memorial Hermann-Texas Medical Center, UTHealth was the first in the country to intravenously inject a stroke patients own stem cells in a trial funded by the National Institute of Neurological Disorders and Stroke, part of the National Institutes of Health. Learn how researchers continue to push the boundaries of this promising field.

UTHealth specialists available for interview

A first-of-its-kind clinical trial studying two forms of stem cell treatments for children with cerebral palsy (CP) has begun at The University of Texas Health Science Center at Houston (UTHealth) Medical School.

Sean I. Savitz, M.D., associate professor of neurology at The University of Texas Health Science Center at Houston (UTHealth), recently received the Molly and Bernard Sanberg Memorial Award from the American Society of Neural Therapy and Repair (ASNTR).

Every year, approximately 795,000 people in the United States suffer a stroke and the late U.S. Senator and Democratic Party vice presidential candidate Lloyd Bentsen was one of them. As the senator and his wife, B. A., dealt with the challenges of stroke, they developed the idea for a stroke research center.

Read the original post:
Stem Cell Research - The UT Health Science Center at ...

Scientists create therapy-grade stem cells using new cocktail to reprogram adult cells

PUBLIC RELEASE DATE:

16-Sep-2014

Contact: Dov Smith dovs@savion.huji.ac.il 972-258-82844 The Hebrew University of Jerusalem @HebrewU

Researchers at the Hebrew University of Jerusalem have developed a new cocktail that is highly effective at coaxing adult cells to become quality pluripotent stem cells.

Regenerative medicine is a new and expanding area that aims to replace lost or damaged cells, tissues or organs through cellular transplantation. Because stem cells derived from human embryos can trigger ethical concerns, a good solution is reprogramming adult cells back to an embryo-like state using a combination of reprogramming factors.

The resulting cells, called induced pluripotent stem cells (iPSCs), could be used to replace those lost to damage or disease. However, scientists have discovered that the process of reprogramming adult cells can introduce genetic abnormalities that limit the cells' usefulness in research and medicine.

To make iPSCs, scientists expose adult cells to a cocktail of genes that are active in embryonic stem cells. iPSCs can then be coaxed to differentiate into other cell types such as nerve or muscle. However, the standard combination of factors used to reprogram cells leads to a high percentage of serious genomic aberrations in the resulting cells. (The reprogramming factors are Oct4, Sox2, Klf4, and Myc known collectively as OSKM).

Now researchers at the Hebrew University of Jerusalem have developed a new cocktail of reprogramming factors that produce high-quality iPSCs. Dr. Yosef Buganim, at the Institute for Medical Research Israel-Canada in the Hebrew University's Faculty of Medicine, worked with scientists at the lab of Whitehead Institute founding member Rudolf Jaenisch, a professor of biology at MIT.

The researchers reasoned that changing the reprogramming factors could reprogram the adult cells in a more controlled way and yield high-quality iPSCs. Working with mouse cells, Dr. Buganim and research scientist Styliani Markoulaki used bioinformatic analysis to design a new cocktail of reprogramming factors (Sall4, Nanog, Esrrb, and Lin28, known collectively as SNEL).

Their results showed that the interaction between reprogramming factors plays a crucial role in determining the quantity and quality of resulting iPSCs and that a different combination of reprogramming factors can in fact produce a much higher quality product.

Read the original post:
Scientists create therapy-grade stem cells using new cocktail to reprogram adult cells

Japan stem-cell trial stirs envy

JIJI PRESS/AFP/Getty Images

Masayo Takahashi is the first to implant tissue derived from induced pluripotent stem cells into a person.

Its awesome, its amazing, Im thrilled, Ive been waiting for this, says Jeanne Loring, a stem-cell biologist at the Scripps Research Institute in La Jolla, California. She is one of several researchers around the world to welcome the news that a Japanese woman with visual impairment had become the first person to receive a therapy derived from stem cells known as induced pluripotent stem (iPS) cells.

A lot rides on this trial. If the procedure proves safe, it could soften the stance of regulatory bodies in other nations towards human trials of iPS cells, and it could pave the way for treatments for other conditions, such as Parkinsons disease and diabetes. It could also cement Japan, recently plagued by a stem-cell scandal, as a frontrunner in iPS-cell research.

Pioneered in 2006 by Shinya Yamanaka, now director of the Center for iPS Cell Research and Applications at Kyoto University, iPS cells are created by inserting certain genes into the DNA of adult cells to reprogram the cells back to an embryonic-like state. The cells can then be turned into almost any tissue type, much as embryonic stem cells can. But because iPS cells can be derived from a patients own tissue, the hope is that they will dodge some of the controversial aspects and safety concerns of those derived from embryos.

In 2012, Yamanaka received a Nobel prize for his work, and the field has now matured, with teams across the world champing at the bit to test therapies based on iPS cells in people. Loring, for example, uses the cells to create dopamine-producing neurons as a potential therapy for Parkinsons disease, and says that she will start clinical trials as soon as the US Food and Drug Administration (FDA) gives the go-ahead.

Still, tissues made from iPS cells carry their own concerns, and that had stopped any country from approving them for a clinical trial. The bodys immune system could attack them, or they might contain some cells that are still in the pluripotent state and cause cancerous growths although Loring points out that this has not happened with human trials of therapies based on embryonic stem cells, for which the same concerns would apply.

In July 2013, however, Japans regulatory authorities gave the go-ahead for a team led by ophthalmologist Masayo Takahashi at the RIKEN Center for Developmental Biology (CDB) in Kobe to collect cells to be used in a clinical iPS-cell pilot study.

His team took skin cells from the first patient, a woman in her seventies who had retinal damage owing to a condition known as age-related macular degeneration. The researchers then reprogrammed the skin cells into iPS cells and coaxed the unspecialized cells into becoming retinal tissue. On 8September, Takahashi provided evidence that those cells were genetically stable and safe, a prerequisite for them to be transplanted into the eye. The procedure took place four days later, and RIKEN has reported that the patient experienced no serious side effects.

In this instance, the womans vision is unlikely to improve. However, researchers around the world are watching to see whether the cells stop the retina from deteriorating further and whether any side effects develop. Should the woman experience serious consequences, iPS-cell research could be set back years, much as gene therapy was in 1999 when a patient died in a trial that attempted to use a modified gene to correct a type of liver disease. That wakes me up at night, Loring admits.

Original post:
Japan stem-cell trial stirs envy

Trials and tribulations of stem cell therapy

Stem cells broke into the public consciousness in the early 1990s, but progress has been slow. Photo: Bloomberg

Edgar Irastorza was just 31 when his heart stopped beating in October 2008.

A Miami property manager, break-dancer and former high school wrestler, Irastorza had recently gained weight as his wife's third pregnancy progressed. "I kind of got pregnant, too," he said.

During a workout one day, he felt short of breath and insisted that friends rush him to the hospital. Minutes later, his pulse flatlined.

He survived the heart attack, but the scar tissue that resulted cut his heart's pumping ability by a third. He couldn't pick up his children. He couldn't dance. He fell asleep every night wondering if he would wake up in the morning.

Desperation motivated Irastorza to volunteer for a highly unusual medical research trial: getting stem cells injected directly into his heart.

"I just trusted my doctors and the science behind it, and said, 'This is my only chance,'" he said recently.

Over the past five years, by studying stem cells in lab dishes, test animals and intrepid patients like Irastorza, researchers have brought the vague, grandiose promises of stem cell therapies closer to reality.

Stem cells broke into the public consciousness in the early 1990s, alluring for their potential to help the body beat back diseases of degeneration like Alzheimer's, and to grow new parts to treat conditions like spinal cord injuries.

Progress has been slow. The Michael J. Fox Foundation for Parkinson's Research, an early supporter of stem cell research, pulled its financial backing two years ago, saying that it preferred to invest in research that was closer to providing immediate help for Parkinson's disease patients.

See the rest here:
Trials and tribulations of stem cell therapy

Global Stem Cells Group Signs Consortia Innovas, SA to Exclusive Representative Contract for Chile Territory

MIAMI (PRWEB) September 15, 2014

Global Stem Cells Group, Inc. has signed an exclusive representative contract with Consortia Innovas, SA, a Santiago, Chile-based health management, development and biotech company. Founded by entrepreneur Enrique Testart, M.D., Consortia Innovas focuses on helping patients gain access to the latest medical treatments regenerative medicine has to offer.

According to Global Stem Cells Group Founder Benito Novas, Testart searches the globe for innovative stem cell companies that fit in with the Chilean markets, and Global Stem Cells Group turned out to be a perfect fit. Innovas will be in charge of all Global Stem Cells Group divisions and programs in Chile, including patient recruiting through Regenestem, physician training and certification trough Stem Cell Training, and stem cell equipment and disposables sales through Adimarket.

Regenestem, Stem Cell Training and Adimarket are all subsidiaries of the Global Stem Cells Group brand.

Our main objective is to organize Chiles first symposium on Stem Cells and Regenerative Medicine in Santiago in early 2015, Novas says. Our new alliance with Consortia Innovas will allow us to establish our brand as the leader in regenerative medicine therapies in Chile.

The first annual Global Stem Cells Symposium is scheduled to take place in Buenos Aires Oct 2, 2014, to be preceded by an intensive two-day hands-on training course in stem cell harvesting, isolation and applications Sept. 27 and 28 at Santiagos Innovas facilities.

The key to Global Stem Cells Groups strategy to expand into foreign markets by recruiting local representatives and distributors like Consortia Innovas to help manage the companys growth in a specific geographic area. Global Stem Cells group requires any company under consideration for the expansion program to have more than five years experience in the health care industry with at least some experience in the field of regenerative medicine .

In addition, geographic alliances require a commitment to a number of stem cell training courses during a one-year period, certification of physicians, and willingness to organize a large medical meeting or symposium in their territory.

To learn more about the Global Stem Cells Group alliance with Consortia Innovas, SA, visit http://www.stemcellsgroup.com, email bnovas(at)stemcellsgroup(dot)com, or call 305.224.1858.

About Global Stem Cell Group:

See the article here:
Global Stem Cells Group Signs Consortia Innovas, SA to Exclusive Representative Contract for Chile Territory