Category Archives: Stem Cell Clinic


Adult stem-cell tech company signs on with Mayo Clinic

Posted: Friday, January 31, 2014 8:30 pm

Adult stem-cell tech company signs on with Mayo Clinic

An adult stem-cell technology company called BrainStorm Cell Therapeutics has signed an agreement with Mayo Clinic in Rochester to conduct its Phase II clinical trial of NurOwn in amyotrophic lateral sclerosis (ALS) patients, pending approval from the U.S. Food and Drug Administration.

The company announced this week that Mayo's Human Cell Therapy Laboratory "will manufacture the NurOwn cells for their clinical-trial participants."

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Adult stem-cell tech company signs on with Mayo Clinic

Family seeks stem cell donors in Meaford for child with leukemia

Meaford Express

By Junior Kindergarten, Katie Star Herron had already beat cancer once.

By 4-years-old, she had been through 25 months of intense treatment for leukemia, including lumbar punctures, bone marrow aspirations, chemotherapy, steroids and more time at the hospital than at home. She received her last does of chemotherapy in September 2012 and was in remission.

But the cancer is back, and now her family is reaching out everywhere they can to find a stem cell donor for Katie. A stem-cell transplant is her only hope.

In some cases, about 30 per cent, there's a compatible donor in the family somewhere.

Katie lives with her parents in Cambridge, but she has extended family in Meaford. Katie's grandparents Georgina (Sewell) and Glenn Hodgkinson grew up in Meaford and they are hoping there might be family left in town who can help their little granddaughter.

One Match is a Canadian registry connected to an international network of stem-cell and bone marrow donor registries, and the family of Katie has arranged for a cheek-swabbing clinic in Cambridge on Saturday, February 22 at the Cambridge Sports Park at 1001 Franklin Boulevard from 1 p.m. to 5 p.m.

The other option for people in Meaford is to register on their own as a donor on One Match by visiting http://www.onematch.ca or calling 1-888-236-6283 to fill out a health questionnaire and receive a swab kit in the mail.

About 70 per cent of stem-cell transplant patients receive donations from strangers and non-family members. So it's important to register as a donor on One Match. By registering at One Match, a donor can give stem cells to a patient anywhere in the world.

Ideal donors are between the ages of 17 and 35 and in good health.

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Family seeks stem cell donors in Meaford for child with leukemia

Scientists in revolutionary stem cell discovery

Wednesday 29 January 2014 22.31

A "revolutionary" new approach to creating stem cells in the laboratory could open up a new era of personalised medicine, it is claimed.

Scientists have shown it is possible to reprogramme cells into an embryonic-like state simply by altering their environment.

It means in principle that cells can have their developmental clock turned back without directly interfering with their genes - something never achieved before.

The cells become "pluripotent", having the potential ability to transform themselves into virtually any kind of tissue in the body, from brain to bone.

Reprogramming a patient's own cells in this way is seen as the Holy Grail of regenerative medicine.

It raisesthe prospect of repairing diseased and damaged organs with new healthy tissue that will not be rejected by the immune system.

Current methods of performing the same trick involve genetic manipulation, which carries with it a serious risk of triggering cancer.

But the new method described in the journal Nature requires no genetic tweaking.

Scientists simply bathed immature white blood cells from mice in an acidic solution for 25 minutes.

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Scientists in revolutionary stem cell discovery

Life or death: Girl in need of stem cell match

Milton Canadian Champion

Anne Hodgkinson and Paul Herron are living every parents worst nightmare. Again.

When their daughter Katie Herron, now four years old, battled cancer as a toddler, the fight for the little girls health was a private, family affair. The youngster endured many months of cancer treatment and battled her way back to a healthy recovery.

That all changed last November.

The Cambridge family doesnt worry about privacy anymore. Theyre now telling everyone they know Katies acute lymphoblastic leukemia is back. Katies life depends on it.

Although the type of cancer that has taken hold of her body usually has a high success rate of responding to treatment, the girl is among the small percentage of children who cant beat the leukemia using standard treatment protocols.

Katies only life-saving option now is to find a stem cell donor match.

Weve got to find a match and weve go to find it soon, explained an emotionally-raw Hodgkinson, as she paced the hallways of Hamiltons McMaster Childrens Hospital, where Katie has lived since the fall.

We have to find a match. She is fighting for her life.

Its hoped a stem cell match would help reboot Katies blood by essentially wiping out her white blood cells and replacing them with a matched transplant of healthy white blood cells. The procedure would enable her body to fight for itself.

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Life or death: Girl in need of stem cell match

Stem cell breakthrough may herald age of personalised medicine

29/01/2014 - 15:56:06Back to World Home

A revolutionary new approach to creating stem cells in the laboratory could open up a new era of personalised medicine, it is claimed.

Scientists have shown it is possible to reprogramme cells into an embryonic-like state simply by altering their environment.

It means in principle that cells can have their developmental clock turned back without directly interfering with their genes something never achieved before.

The cells become pluripotent, having the potential ability to transform themselves into virtually any kind of tissue in the body, from brain to bone.

Reprogramming a patients own cells in this way is seen as the Holy Grail of regenerative medicine, raising the prospect of repairing diseased and damaged organs with new healthy tissue that will not be rejected by the immune system.

Current methods of performing the same trick involve genetic manipulation, which carries with it a serious risk of triggering cancer.

But the new method described in the journal Nature requires no genetic tweaking. Scientists simply bathed immature white blood cells from mice in an acidic solution for 25 minutes.

Tests showed that, stressed in this way, some of the cells lost their blood identity and produced gene markers typical of early embryos.

When these cells were transferred to a special growth-promoting culture medium they began to multiply and acquired features typical of embryonic stem cells.

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Stem cell breakthrough may herald age of personalised medicine

Mayo Clinic Discovery Leads to FDA Approval for Stem Cell Trial for Heart Failure Patients

Dennis Douda (@ddouda) published a blog post January 17th, 2014

Mayo Clinic Discovery Leads to FDA Approval for Stem Cell Trial for Heart Failure Patients

U.S. FDA Approves Phase III Cardiopoietic Stem Cell Trial for Heart Failure Patients Based on a Mayo Discovery

Cardio3 BioSciences, an international Mayo Clinic collaborator, has received FDA approval for a phase III pivotal clinical trial of its stem cell therapy.The trial will test the Mayo Clinic discovery of cardiopoietic (cardiogenically-instructed) stem cells designed to improve heart health in people suffering from heart failure.The multisite U.S. trial, called CHART-2, will aim to recruit 240 patients with chronic advanced symptomatic heart failure. Cardio3 BioSciences is a bioscience company in Mont-Saint-Guibert, Belgium.

"Regenerative medicine is poised to transformthe way we treat patients," says Andre Terzic, M.D., Ph.D., director of the Mayo Clinic Center for Regenerative Medicine. Watch the video below to see how stem cells are being used to treat people with heart failure.

Journalists: Video b-roll of today's news conference, plussound bites with Dr. Terzic and Christian Homsy, M.D., CEO of Cardio3 BioSciences, areavailable in the downloads. The video pkg. is also available in the downloads in MOV format.

Cardio3 Biosciencescardiopoetic Dr. Andre Terzic Dr Terzic Heart heart diseaseregenerative medicine stem cells

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Mayo Clinic Discovery Leads to FDA Approval for Stem Cell Trial for Heart Failure Patients

FASEB announces 2014 Science Research Conference: Skeletal Muscle Satellite and Stem Cells

PUBLIC RELEASE DATE:

22-Jan-2014

Contact: Robin Crawford src@faseb.org 301-634-7010 Federation of American Societies for Experimental Biology

Bethesda, MD This 2014 FASEB Science Research Conference focuses on recent advances in our understanding of the regulatory mechanisms controlling normal and abnormal functions of muscle-resident stem cells in regeneration, muscle homeostasis, hypertrophy, aging and muscle degenerative disease.

Eight plenary sessions and three dedicated poster sessions will encompass the following major themes: transcriptional and posttranscriptional regulation of gene expression in stem cells, satellite cell heterogeneity and potential, stem cell signaling and environmental interactions, satellite cell quiescence, activation and renewal, non-satellite stem cells, satellite cell proliferation, commitment and differentiation, muscle stem cells in growth and hypertrophy, and muscle stem cells in aging, disease and therapeutics.

This FASEB Conference increasingly attracts investigators in related fields who are interested in the rapid advances in muscle stem cell research, and interdisciplinary interactions are an important feature of this meeting. Collectively, this conference, which represents the only international conference that focuses exclusively on muscle satellite and stem cell populations, provides a venue to present cutting edge research, foster discussions, and promote collaborative interactions, with the goal of advancing a fundamental understanding of muscle-resident stem cells, and ultimately, translating this knowledge to the clinic.

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FASEB has announced a total of 35 Science Research Conferences (SRC) in 2014. Registration opens January 17, 2014. For more information about an SRC, view preliminary programs, or find a listing of all our 2014 SRCs, please visit http://www.faseb.org/SRC.

Since 1982, FASEB SRC has offered a continuing series of inter-disciplinary exchanges that are recognized as a valuable complement to the highly successful society meetings. Divided into small groups, scientists from around the world meet intimately and without distractions to explore new approaches to those research areas undergoing rapid scientific changes.

In efforts to expand the SRC series, potential organizers are encouraged to contact SRC staff at SRC@faseb.org. Proposal guidelines can be found at http://www.faseb.org/SRC.

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FASEB announces 2014 Science Research Conference: Skeletal Muscle Satellite and Stem Cells

Stem Cell Clinics USA | Stem Cell Treatment

Stem Cells....Snake Oil or Reality?

Searching for stem cell treatment online will give you a huge number of results often offering unproven, and ill-explained, therapies at overseas clinics. Finding a clinic that offers such services in the US is nigh on impossible as the FDA controls the use of stem cells for both research and therapeutic application very carefully. To some this is a problem because it necessarily slows down the rate of availability of treatments, but for others it can, quite literally, save their lives. Whatever problems the FDA has, you can be pretty confident that undergoing stem cell treatment in the US means having a dedicated, experienced, and professional team of qualified scientists and doctors administering the treatment and handling follow-up care as appropriate. You can also be fairly sure that the stem cell treatments you undergo will have been researched professionally and reviewed extensively before being made available to patients.

Clinics overseas are often unregulated or so transient that they simply move from country to country as the authorities catch up with them. The staff at such clinics may well be highly regarded doctors or scientists who are practicing therapies they feel should be made available to all patients in the US now rather than when the FDA decides they are appropriate. However, in many cases these clinics are more concerned with convincing vulnerable patients to part with their money for treatments that are unlikely to offer any health benefits other than a placebo effect and may in fact be downright dangerous.

Controls on health, hygiene, and safe medical practices may not be followed in countries where the government turns a blind eye to such health tourism. Treatments using embryonic stem cells have been, and still are being used in clinics overseas despite safety concerns regarding the uncontrolled differentiation of these stem cells once injected into the body. The origins of such biological material is also questionable in many cases with the Ukraine implicated, a number of years ago, in a scandal involving dubious procurement of foetuses and infants for stem cell therapies.

Clinical trials exist not in order to frustrate patients awaiting treatment but to safeguard patients from potentially dangerous and mishandled therapy. Even after clinical trials have been carried out and a treatment approved there are still many potential problems that can arise in the much larger number of patients treated than those in the trials themselves. Clinical trials can at least avoid some of the more overt contraindications and highlight the need for further research. They also allow patients to receive treatments which are likely to be efficacious and can be covered by medical insurance.

Travelling overseas for treatments often means invalidating the health-care plan in the US and any complications (such as infection, tumor growth, or paralysis) requiring further treatment or hospitalization when back home are often excluded from such plans. Although many clinics in the US offer stem cell treatments the reality is that patients only have their consultation on US soil and then must travel to a clinic in the Caribbean, Ukraine or other country to actually undergo the treatment as it is not approved by the FDA.

Research trials conducted overseas may offer patients a way of accessing treatment but these should be approached cautiously as the regulation of standards in such trials can vary widely. Again, some researchers are perfectly professional and are simply looking to further the field of regenerative medicine without having to adhere to the seemingly overly stringent restrictions put in place by US regulators. Others however, are adept at engaging in methodologically unsound trials which prove to be little more than anecdotal observation and publishing these in a non-peer-reviewed trade journal of their own making. Claiming that a therapy has been proven to work and has had research published to such effect means very little unless the journal, the paper, and the raw data are readily available for other scientists to review and confirm through repeated experiment.

Stem Cell Treatment overseas is often unregulated and downright dangerous

Clinics in Russia, India, Mexico, and Panama are offering treatments with little, if any, clinical evidence to merit their use. Even in the US there are doctors who are using a loophole in regulations to treat patients with their own stem cells despite there being limited evidence proving any benefit from such treatment. These doctors extract stem cells from fatty tissue using liposuction and minimal processing techniques and then inject the stem cells back into the patient all in an outpatient procedure taking around seven hours or so. This treatment is unlikely to be harmful to a patient but is far from proven to be effective for any disease condition. Indeed, the clinics offering such treatment maintain that it is not intended to treat any pathology and is at best a cosmetic procedure. Clearly the establishment of such clinics and the marketing practices defies this supposed intention and is much more geared toward ill and vulnerable patients.

China, well known for offering stem cell treatments to patients despite a lack of evidence for safety or efficacy, passed a law last May requiring clinical trials prior to such treatments being offered to patients. The degree to which this law is being enforced remains unknown, and, as yet, there have been no public announcements of clinics shut down under the new regulations. There are thought to be around 150 clinics in China which offer stem cell therapy for conditions ranging from spinal cord injuries to Multiple Sclerosis, and diabetes. Patients from the US would expect to pay around $25,000 for treatments in Chinese stem cell clinics although the cost of follow-up treatments and possible rehabilitative care in the US is not included in this price.

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Stem Cell Clinics USA | Stem Cell Treatment

New Assessment Tool Shows Potential of Stem Cells in Restoring LSCD Patients’ Sight

Durham, NC (PRWEB) January 17, 2014

A new assessment tool is helping scientists determine which treatments might benefit patients with a type of eye disorder called limbal stem cell deficiency (LSCD). The tool, developed by researchers at University College London and Moorfields Eye Hospital in London and funded by the UKs National Institute for Health Research Biomedical Research Centre at these institutions, has already shown that the majority of these patients can benefit in the short term from a stem cell transplantation and up to 30 percent are still experiencing better sight three years later, according to the study published in the current issue of STEM CELLS Translational Medicine.

LSCD is an eye disorder in which the stem cells responsible for forming the surface skin of the cornea are destroyed by injury or disease. This results in pain, loss of vision and a cosmetically unpleasant appearance. Many new treatments, including limbal stem cell transplants, are emerging for this condition but their effectiveness remains to be proven.

Assessing how well they perform has been severely hampered by the lack of biomarkers for LSCD and/or validated tools for determining its severity, said Alex Shortt, M.D., Ph.D., of University College Londons Institute of Ophthalmology and lead investigator in the study. In virtually all studies of limbal stem cell transplantation to date the clinical outcome has been assessed subjectively by the investigating clinician. This is clearly open to significant measurement and reporting bias.

His teams aims, then, were to design and test the reliability of a new tool for grading LSCD, to define a set of core outcome measures to use in evaluating treatments and to demonstrate the treatments impact on two common types of LSCD: a genetic disorder called aniridia and Stevens-Johnson syndrome (SJS), an inflammatory disorder.

They began developing an assessment tool by paring down a list of clinical signs taken from previously published studies to four key LSCD indicators: corneal epithelial haze, superficial corneal neovascularization, corneal epithelial irregularity and corneal epithelial defect. A standardized grading plate was then produced for each of these parameters, ranging from normal to severe. They named their assessment method the Clinical Outcome Assessment in Surgical Trials of Limbal stem cell deficiency [COASTL] tool and validated its performance in 26 patients with varying degrees of LSCD.

Once they had the COASTL tool in place, they used it to evaluate treatment outcomes in 14 patients with aniridia or SJS. All had undergone a limbal epithelial transplantation (allo-CLET), using cells taken from a deceased donor, cultivated in the lab before being transplanted into the recipient.

The COASTL tool showed that following allo-CLET there was a decrease in LSCD severity and an increase in visual acuity up to 12 months post-treatment, but thereafter LSCD severity and visual acuity progressively deteriorated, Dr. Shortt said. However, despite a recurrence of clinical signs, the visual benefit persisted in 30 percent of aniridic and 25 percent of SJS patients at 36 months.

A reliable method of obtaining objective outcome data for surgical trials of limbal stem cell deficiency will greatly contribute to the effective evaluation of current and new treatments, said Anthony Atala, M.D., editor of STEM CELLS Translational Medicine and director of the Wake Forest Institute for Regenerative Medicine.

The full article, Three-Year Outcomes of Cultured Limbal Epithelial Allografts in Aniridia and Stevens-Johnson Syndrome Evaluated Using the Clinical Outcome Assessment in Surgical Trials Assessment Tool, can be accessed at http://www.stemcellstm.com.

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New Assessment Tool Shows Potential of Stem Cells in Restoring LSCD Patients’ Sight

Stem cells: What they are and what they do – Mayo Clinic

Stem cells: What they are and what they do Stem cells and derived products offer great promise for new medical treatments. Learn about stem cell types, current and possible uses, ethical issues, and the state of research and practice. By Mayo Clinic Staff

You've heard about stem cells in the news, and perhaps you've wondered if they might help you or a loved one with a serious disease. You may wonder what stem cells are, how they're being used to treat disease and injury, and why they're the subject of such vigorous debate.

Here are some answers to frequently asked questions about stem cells.

Researchers and doctors hope stem cell studies can help to:

Generate healthy cells to replace diseased cells (regenerative medicine). Stem cells can be guided into becoming specific cells that can be used to regenerate and repair diseased or damaged tissues in people.

People who might benefit from stem cell therapies include those with spinal cord injuries, type 1 diabetes, Parkinson's disease, Alzheimer's disease, heart disease, stroke, burns, cancer and osteoarthritis.

Stem cells may have the potential to be grown to become new tissue for use in transplant and regenerative medicine. Researchers continue to advance the knowledge on stem cells and their applications in transplant and regenerative medicine.

Test new drugs for safety and effectiveness. Before using new drugs in people, some types of stem cells are useful to test the safety and quality of investigational drugs. This type of testing will most likely first have a direct impact on drug development for cardiac toxicity testing.

New areas of study include the effectiveness of using human stem cells that have been programmed into tissue-specific cells to test new drugs. For testing of new drugs to be accurate, the cells must be programmed to acquire properties of the type of cells to be tested. Techniques to program cells into specific cells continue to be studied.

For instance, nerve cells could be generated to test a new drug for a nerve disease. Tests could show whether the new drug had any effect on the cells and whether the cells were harmed.

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Stem cells: What they are and what they do - Mayo Clinic