Category Archives: Stem Cell Treatment


Cell Therapy 2.0: Reprogramming the Brain’s Own Cells for Parkinson’s Treatment – Scientific American

For the past five decades pharmaceutical drugs like levodopa have been the gold standard for treating Parkinsons disease. These medications alleviate motor symptoms of the disease, but none of them can cure it. Patients with Parkinsons continue to lose dopamine neurons critical to the motor control centers of the brain. Eventually the drugs become ineffective and patients tremors get worse. They experience a loss of balance and a debilitating stiffness takes over their legs.

To replace the lost dopamine neurons, scientists have begun investigating stem cell therapy as a potential treatment or even a cure. But embryonic cells and adult stem cells have proved difficult to harness and transplant into the brain.

Now a study from the Karolinska Institute in Stockholm shows it is possible to coax the brains own astrocytescells that typically support and nurture neuronsinto producing a new generation of dopamine neurons. The reprogrammed cells display several of the properties and functions of native dopamine neurons and could alter the course of Parkinsons, according to the researchers. You can directly reprogram a cell that is already inside the brain and change the function in such a way that you can improve neurological symptoms, says senior author Ernest Arenas, a professor of medical biochemistry at Karolinska. Previously, scientists had to nudge specialized cells like neurons into becoming pluripotent cells before they could develop a different kind of specialized cell, he says. It was like having to erase all the written instructions for how a cell should develop and what job it should do and then rewriting them all over again. But Arenas and his team found a way to convert the instructions into a different set of commands without erasing them.

By adding a cocktail of three genes and a small RNA moleculeNEUROD1, ASCL1, LMX1A and miR-218, respectivelythe researchers forced astrocytes to transform directly into dopamine neurons. In culture, once human astrocytes were successfully reprogrammed this way, they looked and acted just like normal midbrain dopamine neurons. The reprogrammed cells grew axons, the long fibers that make connections with other neurons, fired electrical signals and released dopamine.

In mice, researchers first destroyed dopamine neurons in one part of the brain to produce a model of Parkinsons. Then they injected the cocktail of genes into the brain and observed the mice as they walked on a tiny treadmill. Within five weeks the mice began to walk straighter, their movements were more coordinated and their posture was improved.

The results, which were published in Nature Biotechnology today, open the door to a novel therapeutic approach for Parkinsons. Directly converting astrocytes already present in patients brains could eliminate the need to search for donor cells as well as avoid the risk of immunosuppression of transplanted cells. The treatments would also produce proteins involved in normal cellular processes and may therefore be less likely to cause side effects compared with current drugs. This is like stem cell 2.0. Its the next-generation approach to stem cell treatments and regenerative medicine, says James Beck, vice president and chief scientific officer, for the nonprofit Parkinsons Disease Foundation who was not involved with the research.* An estimated one million Americans and more than 10 million people worldwide live with Parkinsons. Replacing their lost dopamine neurons with reprogrammed brain cells could make management of their motor symptoms much easier, he notes. Instead of having to take eight pills or more every day in the later stages of the disease, people could reduce the amount of medication they have to take, maybe even down to zero.

But there are some caveats: Unfortunately, this is not going to halt the course of Parkinsons, Beck warns. If patients lose more dopamine neurons as the disease progresses, scientists or physicians may have to repeat the process of reprogramming replacement cells. And the disease often affects more than just dopamine neurons. There is a whole host of nonmotor symptoms that accompany Parkinsons, including cognitive impairment, depression, gastrointestinal complications and autonomic dysfunction. Motor improvement is only half the battle, according to Beck.

Researchers need to ensure the cocktail of added genes is standardized and produces robust cells in further tests. They will also need to verify that the process does not change other cells in the brain before it is ready for human clinical trials. Only a few small fetal and stem cell graft trials have been conducted so farand with mixed results, Beck said. But although this direct-reprogramming technique is being developed in parallel to stem cellbased therapies, it could be instructive as well as improve from clinical trials, eventually replacing stem cell therapy in the next decade, he adds. This is an insight into what the future of Parkinsons treatment holds.

*Editor's Note (04/11/17): This sentence was edited after posting to update James Beck's title.

Read more here:
Cell Therapy 2.0: Reprogramming the Brain's Own Cells for Parkinson's Treatment - Scientific American

Spray-On Skin: ‘Miracle’ Stem Cell Treatment Heals Burns Without Scarring – Newsweek

Pennsylvania state trooper Matt Uram was talking with his wife at a July Fourth party in 2009 when a misjudged spray of gasoline burst through a nearby bonfire and set him alight. Flames covered the entire right side of his body, and after he fell to the ground to smother them, his wife beat his head with her bare hands to put out his burning hair. It was only on the way to the ER, as the shock and adrenaline began to wear off, that the pain set in. It was intense, he says. If you can imagine what pins and needles feel like, then replace those needles with matches.

From the hospital, Uram was transferred to the Mercy Burn Center in Pittsburgh, where doctors removed all of the burned skin and dressed his wounds. It was on the border between a second- and third-degree burn, and he was told to prepare for months of pain and permanent disfigurement. Not long after this assessment, however, a doctor asked Uram if he would be willing to take part in an experimental trial of a new device.

The treatment, developed by German researcher Dr. Jrg Gerlach, was the worlds first to use a patients stem cells to directly heal the skin. If successful, the device would mend Urams wounds using his bodys ability to regenerate fully functioning skin. Uram agreed to the procedure without hesitation.

Five days after the accident, surgeons removed a small section of undamaged skin from Urams right thighabout the size of a postage stampand used it to create a liquid suspension of his stem cells that was sprayed in a fine mist onto the damaged skin. Three days later, when it was time to remove the bandages and re-dress the wounds, his doctor was amazed by what he saw. The burns were almost completely healed, and any risk of infection or scarring was gone.

Pennsylvania State Trooper Matt Uram's arm eventually healed without scarring. RenovaCare

A study subsequently published in the scientific journal Burns described how the spray was able to regrow the skin across the burn by spreading thousands of tiny regenerative islands, rather than forcing the wound to heal from its edge to the inside. The technique meant reducing the healing time and minimizing complications, with aesthetically and functionally satisfying outcomes, the paper stated.

Dozens more burn victims in Germany and the U.S. were successfully treated with the spray following Urams procedure, and in 2014 Gerlach sold the technology to RenovaCare. The medical technology startup has now transformed the proof-of-concept device from a complicated prototype into a user-friendly product called a SkinGun, which it hopes clinicians will be able to use outside of an experimental setting. For that to happen, RenovaCare is preparing clinical studies for later this year, with the aim of Food and Drug Administration approval for the SkinGun.

Once these obstacles are overcome, RenovaCare CEO Thomas Bold believes, the SkinGun can compete with, or even replace, todays standard of care.

Current treatment of severe burns involves transplanting healthy skin from one area of the body and stitching it to another in a process called skin grafting or mesh skin grafting. It is a painful procedure that creates an additional wound at the donor site and can cause restricted joint movement because the transplanted skin is unable to grow with the patient. It is able to cover an area only two to three times as large as the harvested patch. The current standard of care is just horrible, says Bold. We are part of regenerative medicineit is the medicine of the future and will be life-changing for patients.

RenovaCare's SkinGun sprays a liquid suspension of a patient's stem cells onto a burn or wound in order to regrow the skin without scars. RenovaCare

Beyond regulatory matters, there are also limitations to the technology that make it unsuitable for competing with treatments of third-degree burns, which involve damage to muscle and other tissue below the skin. Still, stem cell researcher Sarthak Sinha believes that while the SkinGun may not be that advanced yet, it shows the vast potential of this form of regenerative medicine. What I see as the future of burn treatment is not skin repair but rather functional regeneration of skin and its appendagessuch as hair follicles, glands and fat, says Sinha. This could be achieved by engaging deeper layers of skin and its resident stem cells to partake in tissue regeneration.

Research is already underway at RenovaCare to enable treatment of third-degree burns, which Bold describes as definitely within the range of possibility. Bold claims the adaptations to the SkinGun would allow it to treat other damaged organs using a patients stem cells, but for now the company is focusing solely on burns and wounds to skinthe largest organ of the human body.

Urams burns are now completely unnoticeable. There is no scar tissue or even pigment discoloration, and the regenerated skin even tans. If I show someone where I was burnt, I bet $100,000 they couldnt tell, he says. Theres no scars, no residual pain; its like the burn never happened. Its a miracle.

Uram is frustrated that the treatment is not available to other burn victims, particularly children. I want to see the FDA get off their butts and approve this, he says. A grown man like me to be scarred is OK, but think about the kids that have to live the rest of their lives with pain and scarring. Thats not OK.

Read the original post:
Spray-On Skin: 'Miracle' Stem Cell Treatment Heals Burns Without Scarring - Newsweek

Stem Cell Transplant – Treatment – Patient Care …

Patient Care Treatment

Dr. Krishna Komanduri talks with a patient in the inpatient stem cell transplant unit.

The Adult Stem Cell Transplant Program treats patients with various types of cancer and hematological diseases, including:

The program operates a pre- and post-transplant outpatient clinic as well as an inpatient unit at Sylvester Comprehensive Cancer Center/UMHCUniversity of Miami Hospital & Clinics. The 13,964-square-foot inpatient unit opened at Sylvester/UMHC in 2011 with six apheresis chairs, twelve specialized transplant beds, and seven ICU beds.

The Adult Stem Cell Transplant Program (SCTP), which treats patients from 17 to 75 years old, is led by Krishna Komanduri, M.D., who also co-leads the Tumor Immunobiology Program at Sylvester. The Adult Stem Cell Transplant Program was established in 1992 and is accredited by the Foundation for the Accreditation of Cellular Therapy (FACT). In May 2010, Sylvester opened an Outpatient Clinic designed for the unique needs of stem cell transplant patients. This outpatient treatment center has a dedicated waiting room and phlebotomy area, as well as 10 exam rooms with capability for handling infusions and transfusions required for the care of recently transplanted patients.

Before starting any type of treatment, you will meet with one of our transplant physicians and other members of our multidisciplinary transplant team to determine if a stem cell transplant is recommended for you.

To support stem cell research for cancer, Sylvester dedicated the Kalish Family Endowed Chair in Stem Cell Transplantation in 2010. The generous gift of the Kalish family will support Dr. Komanduris clinical and academic activities. Dr. Komanduris laboratory research is currently supported by grants from the National Institute of Health and the Bankhead-Coley Research Program.

The Sylvester Adult Stem Cell Transplant Program also offers opportunities to participate in clinical trials, including those developed by the Bone Marrow Transplant Clinical Trials Network, a consortium of academic stem cell transplant programs.

The National Marrow Donor Program has established recommendations regarding the appropriate timing for a stem cell transplant consultation. Visitwww.bethematch.org for more information.

Before starting any type of treatment, you will meet with one of Sylvester/UMHCs transplant physicians and other members of our multidisciplinary transplant team to determine if a transplant is recommended for you.

Read the original post:
Stem Cell Transplant - Treatment - Patient Care ...

Fundraiser for Galway girl’s life-changing stem cell treatment – Connacht Tribune Group

Nicola Lavin, nee Glynn, who is originally from Menlo, was diagnosed with Lyme Disease last year following a 16-year battle with an invisible bacteria which has attacked her organs and her immune system.

A table quiz will take place at Monroes Tavern, Dominick Street, next Thursday night (April 13) to support the young Galway mother who is suffering from the debilitating disease.

Nicola (38) can trace her troubles back to a bite from a tick during a summer in New York in 2000.

This resulted in heart failure while she was pregnant with her son, but she was only correctly diagnosed by a laboratory in Germany last year.

Over the years, her health has deteriorated so much that she is unable to work in the career she loves and has no quality of life. At times, she can barely comb her hair or brush her teeth.

Stem cell treatment in Germany can change Nicolas life and give her a second chance. Her friends and family have rallied around Nicola to organise this table quiz in a bid to transform her life. The treatment will cost 23,000.

A table quiz will take place in Monroes on Thursday April 13th at 8pm to help raise the much needed funds that will make such a difference. Donations can also be made through Go Fund Me.

The rest is here:
Fundraiser for Galway girl's life-changing stem cell treatment - Connacht Tribune Group

Study: heart failure stem cell therapy safe, shows early signs of effectiveness – The San Diego Union-Tribune

A stem cell treatment for heart failure patients is safe and shows early signs of effectiveness, according to a study published Wednesday.

The study was conducted by Japanese researchers in 27 patients, who received transplants of stem cells taken from their own thigh muscles. There were no major complications, and most patients showed considerable improvement in their symptoms.

The study was published in the open-access Journal of the American Heart Association. Dr Yoshiki Sawa of Osaka University Graduate School of Medicine was the senior author. It can be found at j.mp/stemheart.

However, two San Diego cardiologists who do stem cell research on heart disease cautioned that similar clinical trials have shown promise over the years, only to fail at the end for various reasons. There is no approved stem cell therapy for heart failure.

So while the trial itself appears to be well-conducted, the researchers are very far from actually proving their treatment is effective, said Dr. Richard Schatz of Scripps Health and Dr. Eric Adler of UC San Diego School of Medicine.

For one thing, the trial was small, they said, and larger trials are where the most rigorous scientific evaluations are made.

These early trials have looked beneficial in the past, Adler said. When we do the larger trials, the results are more equivocal.

Adler said the signs of efficacy in this trial are modest. For example, the change in ejection fraction, a measurement of efficiency in pumping blood, rose from 27 percent to 30 percent in 15 of the 27 patients. Their heart failure was associated with a lack of blood flow, or ischemia. The remaining non-ischemic patients actually had a slight decline.

The entire field of stem cell and regenerative therapy for heart disease has been a disappointment to date, Schatz said.

Weve been at it for 20 years now, and we dont have a product or a positive (late-stage) trial, so that tells you pretty much everything you need to know, he said. Its not for lack of trying or billions of dollars invested. Its just very, very difficult.

The cardiac field has had more success with other technologies, such as cardiac stents. Schatz is the co-inventor of the first stent.

In the study, the researchers acknowledge that previous attempts had only been modestly effective. They devised a method of producing sheets of muscle stem cells and attaching them to the inner layer of the sac that encloses the heart, a layer that rests directly on the heart surface.

The stem cell sheets stimulate healing by producing chemicals that stimulate cardiac regeneration, the study said. The cells themselves dont survive in the long term, but by the time they die they have served their purpose.

Loss of function

Heart failure is a progressive disease in which the heart gradually loses its ability to pump blood. This can be triggered by a heart attack or any other cause that damages the heart muscle.

When damaged heart muscle is replaced with scar tissue, as often happens, the heart loses pumping capacity. It becomes overstressed, and its output of blood declines. This limits the patients ability to engage in intensive physical activity. In advanced cases, patients may become bedridden.

Existing treatments include drugs and LVAD units, which take over some of the hearts function to relieve stress. Some drugs may help the heart work more efficiently, but none have been shown to improve heart failure by actually regenerating lost heart muscle.

Stem cell therapy is tested in patients who havent responded well to other treatments. Trials have been and are being conducted in San Diego area hospitals.

Scripps Health has been testing a cardiac stem cell therapy from Los Angeles-based Capricor. The cells, taken from donor hearts, are injected into the coronary artery, where they are expected to settle in the heart and encourage regrowth.

UC San Diego is testing a heart failure therapy from Teva Pharmaceutical Industries. It consists of bone marrow derived mesenchymal precursor cells. These can give rise to several different cell types, including muscle cells.

And many other trials are going on throughout the country and internationally.

Adler and Schatz said theres reason for optimism in the long run, as technologies improve.

Just because the other trials have been negative doesnt mean this technique wont be beneficial, Adler said. Its just too early to tell.

That said, Schatz emphasized that the nature of the three-phase clinical trial process means that the show-stoppers for a treatment typically appear late.

Tighter standards needed

Clean trials trials where we all agree that this is the patient population we want to look at, are needed, he said.

For example, heart failure comes in two types, he said. Ischemic heart failure is caused by heart attacks and blocked arteries, which impede blood flow. Non-ischemic heart failure can be caused by damage from diseases, such as a virus.

Non-ischemics can be younger people, in their 20s and 30s, while the ischemic patients are older. Mixing those patient groups in a single trial is a mistake, he said.

Theyre different animals, Schatz said.

Another pitfall is failing to screen carefully enough to enroll only patients likely to benefit, Schatz said.

You can have a patient who has chest pain, and coronary disease just incidentally, he said.

His shoulder or chest pain is from a virus. So he goes into the trial and gets a placebo injection in his arm of cortisone, and his arm pain goes away. And because hes in that placebo group, hes counted as a success the pain went away. It has nothing to do with his heart. Thats an extreme example, but we actually saw that happen.

In a failed gene therapy trial for heart disease, some patients apparently had received the injection in the wrong location, missing the heart muscle, Schatz said.

You assume they got the gene, but they didnt, Schatz said. The study was negative, and thats why I think it was negative.

Such errors dont show up in Phase 1 trials, Adler and Schatz said, because theyre focused on evaluating safety. And these early trials dont have many patients, there arent enough to comfortably determine the therapy is really effective.

By the last stage of the trial, these sources of error have often been identified and trial standards have tightened up. And thats when the faulty assumptions made early appear as the trial ends in failure.

Despite those forbidding hurdles, Adler said research should continue.

This disease is killing a lot of people. Theres not going to be enough hearts to go around for transplant. Theres six million Americans with heart failure, and theres 2,000 heart transplants a year. So coming up with novel regenerative cell-based therapy is something were still excited about.

bradley.fikes@sduniontribune.com

(619) 293-1020

More here:
Study: heart failure stem cell therapy safe, shows early signs of effectiveness - The San Diego Union-Tribune

Stem Cell Therapy for Autism Shows Promise – WebMD

April 6, 2017 -- A stem cell treatment for autism shows promise, according to a new study, but the investigators and other experts emphasize that the therapy is still in the early stages and much more research is needed.

The Duke University study included 25 children, ages 2-6, with autism and assessed whether a transfusion of the youngsters' own umbilical cord blood containing rare stem cells would help treat their autism, CNN reported.

Behavioral improvements were reported in 70 percent of the patients, according to the study in the journal Stem Cells.

A second, larger trial is now underway and the researchers hope they will find a long-term treatment for autism, CNN reported.

Some experts say many unanswered questions remain and the study authors agree much more work needs to be done. This initial trial was a safety study, meaning doctors and the children's families knew the therapy was being administered and there was no comparison between treated and non-treated children.

"Some children, who were not speaking very much, had big increases in their vocabulary and their functional speech," study author Dr. Joanne Kurtzberg, head of the Robertson Clinical and Translational Cell Therapy Program, told CNN.

"Many children were able to attend to play and have meaningful communication in a way that they weren't before. Some children had less repetitive behaviors than they did when they came onto the study," Kurtzberg said.

"The study was very encouraging. We did see positive results. However, it did not have a comparison group, which is very important in establishing whether a treatment is actually effective," study author Dr. Geraldine Dawson, director of the Duke Center for Autism and Brain Development, told CNN.

WebMD News from HealthDay

Visit link:
Stem Cell Therapy for Autism Shows Promise - WebMD

Stem cell treatment begins for dystrophy patients from Bangladesh … – Daily News & Analysis

Three Bangladeshis suffering from a highly debilitating muscular dystrophy, who arrived in Mumbai on Sunday have begun their treatment at a Navi Mumbai spine clinic.

Abdus, Rahinul and Shorab aged 24, 14 and 8 respectively were diagnosed with this crippling disease at the time of their birth.

They arrived on Sunday evening and we started the treatment on Monday, said Avantika Patil, spokesperson NeuroGen Brain and Spine Institute in Seawoods, Navi Mumbai, who is treating them for free.

They are undergoing an autologous bone marrow derived stem cell treatment. Stem cells are taken from the bone marrow in their hip bone, treated in our lab and then injected into to the patients again. We will provide a combination of stem cell therapy and neuro-rehabilitation which will also includes yoga and speech therapy sessions, Patil explained.

While the hospital is not willing to say what kind of progress can be expected in these particular cases, they revealed that in one case, a bed-ridden patient was able to walk slowly after six years of treatment.

In January, fruit seller Tofazzal Hossain sparked a rare debate about euthanasia in conservative Bangladesh in January when he pleaded with the authorities to allow his grandson and two sons to die.

See the original post:
Stem cell treatment begins for dystrophy patients from Bangladesh ... - Daily News & Analysis

Stem cells offer hope for autism – CNN

It wasn't always so. Just a couple years ago, Ryleigh, 11, was scared of her sister when she'd throw tantrums and screaming fits.

"She would've fought and kicked," Ryleigh says, noting that it wouldn't have been possible to sit like this next to Gracie.

Gracie, 7, interrupts: "I don't even remember it."

"We do," says her mother, Gina Gregory.

Gracie has autism, a condition that affected nearly every aspect of her family's life after she was diagnosed at 2. But a new study is offering hope for the Gregorys and families like them.

The results were impressive: More than two-thirds of the children showed reported improvements. A larger second trial is underway, one its researchers hope will lead to long-term treatment for children with autism.

But for the Gregorys, the change in their daughter has been monumental.

Gone are the days of Gracie throwing fits in long lines at Disney World or during dinner at restaurants. When a tantrum intruded on family outings, her mom and dad wished they had T-shirts that said "My kid has autism" to ward off judgmental stares.

During autism therapy sessions, Gracie would kick, scream, spit and hit at her occupational therapist. "It was horrible to try to get her to sit there," her mother says.

Even just brushing her teeth or combing her hair could set her off.

Gracie, then 5, was on the mild to moderate autism scale, but her parents say the disorder consumed about 75% of their daily routine. After her participation in the study, that figure has been reduced to a mere 10%.

On a scale of 1 to 10, they rate her improvement around an 8 or 9; it's been that dramatic. She's even begun attending a "regular" school and thriving there, something her parents never thought possible. She'd been in various specialized school programs, and nothing was the proper fit.

Are Gracie's changes a result of the cord blood transfusion stimulating her brain? Or did her brain just mature as she got older? Could it be that her parents were subconsciously determined to magnify her improvements, given all their family had been through?

Those are questions the Gregorys still ask. But they do know that their daughter's transformation appeared to begin about six months after her transfusion in January 2015 and has continued ever since.

Her father's favorite adjustment is her newfound affection. Instead of shunning hugs, she now welcomes an embrace.

"We will say we don't think it's cured her. You still see some of the small idiosyncrasies that she does have," says her father, Wade Gregory. "But again, I think it's supercharged her learning curve. It's pushed her to do things she normally wouldn't do."

Her mother adds, "She got better, and we're just thankful for that -- whether it be the stem cells or not. We're just thankful for what changes have happened."

Each unit is designated by labels with specially designed adhesive to withstand extremely cold temperatures for decades. There are 14 cord blood freezers in all.

It is the cord blood in those freezers -- stored or donated by parents in case a serious illness develops -- that's at the cutting edge of this research.

About 30% never learn to speak, and many children even with early behavioral interventions still struggle to adapt. There also are no FDA-approved medications that improve the core symptoms of autism.

"I was very interested in collaborating with people here at Duke who could offer medical approaches that could enhance neuroplasticity, or the brain's ability to respond to treatment," Dawson says.

"We've been able to show that with some of these diseases, a cord transplant rescues them from death and also improves their neurologic outcome," she says.

She began wondering: Could cord blood help other children?

About a decade ago, her laboratory began clinical tests of children with cerebral palsy whose parents had banked their cord blood. Again, they saw positive results. And in some of those children who had autistic tendencies, they saw autistic symptoms improve. Another spark went off: What if they tested cord blood specifically for autism?

The safety trial began a little over a year and a half ago. Not only did it find cord blood to be safe, but 70% of the 25 children, age 2 to 6, had behavioral improvements as described by their parents and tracked by the Duke researchers. The research is largely funded by a $40 million donation from the Marcus Foundation, a nonprofit created by Home Depot co-founder Bernie Marcus.

The children traveled to Duke three times over the course of a year. They underwent a series of evaluations such as autism assessments, MRIs and EEGs to track their brain activity. On the first trip, the children received the cord blood infusion along with the intense evaluations. Each child received 1 billion to 2 billion cells, given through an IV in their arms or legs. At six months and then a year later, the children returned for more tests and observations.

"Some children, who were not speaking very much, had big increases in their vocabulary and their functional speech," Kurtzberg says. "Many children were able to attend to play and have meaningful communication in a way that they weren't before. Some children had less repetitive behaviors than they did when they came onto the study."

Adds Dawson, "The study was very encouraging. We did see positive results. However, it did not have a comparison group, which is very important in establishing whether a treatment is actually effective."

Both researchers can't stress that enough: that although they're cautiously optimistic about the results, they want the science to play out. They are now in the midst of the definitive trial on whether cord blood can treat autism -- a double-blind, placebo-controlled trial involving 165 autistic children, ranging in age from 2 to 8. The FDA has oversight of the study.

During the phase II study, the children on their first visit receive a cord blood infusion -- either their own or from a donor -- or they get a placebo. They also undergo a battery of assessment tests and brain monitoring.

On their second visit six months later, the children receive a second infusion with whatever preparation they did not receive the first time and undergo more evaluations. The order of the infusions is not known. Researchers will monitor them for the next year for any sign of behavioral improvements.

It's known as a crossover trial, in which each subject gets the treatment and the placebo but in a different order. Researchers say it would have been nearly impossible to find participants if parents knew that their children might not receive an infusion.

How groundbreaking would it be if the trial shows similar results to the safety study?

"If we can show that receiving an infusion of cord blood is more effective for improving social behavior than the placebo," Dawson says, "then this will be game-changing."

Kurtzberg adds, "We'll be extraordinarily encouraged if the second trial shows that the cells benefit children when the placebo does not. We will consider that a breakthrough."

Both researchers were shaped early in life by the struggles families face raising autistic children. As a teen, Dawson babysat twins with autism who lived across the street. "It was just an inspiration to devote my career to improving the lives of people with autism," she says.

Kurtzberg was similarly affected. When she was a junior in college, she would visit a girl with severe autism and play with her as a means of behavioral intervention. "The family still writes to me," she says.

It is for this reason -- their longtime devotion to families raising children with autism -- that both issue a heap of caution. Although they're excited about the results of the first study, Kurtzberg says, "we don't want to mislead people and claim it's working before we have definitive proof."

Adds Dawson, "It's important for parents who might hear about cord blood as a potential treatment for autism to know that we are working very hard to know the answer to that question. We aren't there yet."

Kurtzberg has a hypothesis about what may be happening: that certain immune cells within the cord blood are crossing the blood-brain barrier and altering brain connectivity while also suppressing inflammation, which may exist with autism.

"I feel more confident now because of our (cerebral palsy) study, which preceded this study and does show benefits," Kurtzberg says.

"One has to be very careful when interpreting results that haven't come from properly controlled, double-blind studies," he said. "All I can say is that it would be wonderful if this treatment was effective, but one has to be very cautious before reaching any conclusions."

Even without a placebo effect, he says, many factors could have resulted in an improved outcome in the first study: The growing children could have acquired skills simply through maturation, possibly enhanced by occupational therapy, and their parents may have clung to positive gains, creating a biased outcome.

Kriegstein of UCSF also wonders whether cord blood is really stimulating cells in the brain and creating new connections. "There are so many unanswered questions about what might be going on here, it becomes very difficult to evaluate the proposed mechanism," he said.

"The question remains: How do these cells injected intravenously wind up in the brain, how do they target the appropriate brain regions, and what are they doing that could improve brain function?"

An 8-year-old boy with autism sits at a table in a room within Duke's Center for Autism and Brain Development. Clinical research specialist Michelle Green watches from behind a two-way mirror. Two cameras in the room feed computer monitors, allowing her to further analyze his behavior.

Dr. Lauren Franz, a clinician, works with the boy in the room.

"What kind of things make you feel threatened or anxious?" she asks.

"Like when I'm done with a test," the boy says.

"How does it feel when you're frightened or anxious? How does that feel?"

"Like pretty weird," he says.

The boy is participating in the second trial, and he's returned for his six-month assessment and second infusion. Researchers don't know which infusion he received first: the cord blood or the placebo.

But they track, record and monitor the slightest of details. Although it might seem like an innocuous conversation, researchers will compare the results with those of his first visit and any follow-ups. Was he able to sit still at the table before? Could he articulate his thoughts? Did he talk before the study? Has he improved?

At the Gregorys' home in Florida, Gracie's parents remember when she went through those same tests. The best investment they ever made, they say, was the $2,000 spent on banking her cord blood. At the time, it was just a precaution; her autism diagnosis didn't come until three months after her second birthday.

They know the desperation of families raising a child with autism -- of longing for their daughter to have a shot of normalcy in life. "You can't quantify it. You can't measure it. You want to see your child succeed," her father says.

Mom and Dad recently watched old home videos, of Gracie singing inaudibly, of her covering her ears when "Happy Birthday" was sung for her third birthday, of showing no emotion on Christmas when she was 2. "I forgot how bad it was," her mother says.

They hope the current study leads to similar successes -- and results in breakthrough treatment for autistic children everywhere.

Visit link:
Stem cells offer hope for autism - CNN

Stem-cell therapy is poised to disrupt the Tommy John epidemic in baseball – Quartz


Quartz
Stem-cell therapy is poised to disrupt the Tommy John epidemic in baseball
Quartz
For about half a decade, it's been something of an open secret in baseball that playerspitchers especiallyregularly undergo stem-cell therapy to stave off surgeries and lost playing time. It's a cutting-edge medical procedure, done by everyone from ...

Read this article:
Stem-cell therapy is poised to disrupt the Tommy John epidemic in baseball - Quartz

The Shady Business Of Experimental Stem Cell Treatments – Worldcrunch

GENEVA At the Geneva University Hospitals, pneumologist Jean-Paul Janssens receives patients suffering from Amyotrophic Lateral Sclerosis (ALS). This rare disease is caused by the degeneration of motor neurons and kills patients within a few years. It is incurable.

And yet patients often receive invitations from private clinics or doctors promising a miracle cure using stem cells, which can be multiplied in specialized settings or surfaces. "Patients are ready to enter into any protocol or clinical trial rather than stay inactive. Even if it means overstepping clinical research rules," says Janssens.

The pneumologist tries to warn patients about the illegal nature of the untested stem-cell treatments. Some listen. But others, usually those with more money to spend, try their luck anyway. Janssens remembers one patient, a few years back, who accepted an offer from a clinic in Tel Aviv in Israel. The treatment cost him 35,000 Swiss francs (a little under 33,000 euros). The plan was to remove some of his cells in French-speaking Switzerland, send them for isolation and cultivation in Israel, and then send the cells back to Switzerland for injection.

"We realized this was a bad procedure when the Swiss clinic refused to remove the cells," the doctor recalls. "So the patient had to go to Israel, but his condition prevented him from making the trip. A family member went instead to give his cells. The Swiss clinic then withdrew from the protocol, so the stem cells were injected into the patient at home." He died a short while later, for reasons "unrelated to this treatment," says Janssens.

A global affair

That kind of desperation on the part of patients is boosting a growing market for clinics that offer non-approved stem-cell treatments for conditions such as ALS, multiple sclerosis, Parkinson's disease, diabetes or heart attacks. Already well established in some developing countries, these kinds of clinics are now despite the presence of powerful health agencies regulating the pharmaceutical market gaining a foothold in places like Switzerland, Australia, Italy, Japan or in U.S. states like Florida or California.

In an article published last June in the review Cell Stem Cell, bioethicist Leigh Turner of the University of Minnesota counted 570 clinics illegally offering such treatments, a number big enough to exert economic power and bend laws in the sector's favor.

The clinics often look very respectable.

In Switzerland, investigations led in recent months by the Swiss Agency for Therapeutic Products (Swissmedic) led to authorities to ban two clinics, Med Cell Europe and Swiss Medica, from offering these treatments, and to identification of Intercare as a brokering service. While Stem Cell Europe has ceased all activity in Switzerland, Swiss Medica continues to recruit patients in its premises in Saint Gall, whence they are sent to affiliated centers in Serbia or Russia to undergo treatments banned in Switzerland.

Networking between patients, brokers, clinics and doctors is "what is making things difficult" says Christian Schaerer, head of investigations at Swissmedic. He says such treatments are not in any case offered by well-known clinics, and "can be done in a hotel room" where a foreign guest has brought in a doctor. "It's quite a global affair through international websites where a patient can search for a treatment or doctor, or choose a clinic of interest from among various proposed worldwide," he says.

A sample of stem cells for research conducted in Germany Photo: Oliver Berg/DPA/ZUMA

No reliable data

Clinics like to wrap themselves in legitimacy by stating with the backing of scientific references that their treatments work. Doctors practicing them are raised to the level of pioneers of the new age of regenerative medicine, all in a discourse that tends to ignore the lack of reliable clinical data, not to mention documented and serious risks to patients, like pulmonary embolism, heart attacks, tumors or blindness.

Leigh Turner says the clinics often look very respectable. They cite studies published in scientific journals, he says, and provide guarantees on the doctors they employ. But unless patients make the effort to actually look at those studies, they don't know that the only research done "is on mice," the University of Minnesota bioethicist explains.

In the United States, this illegal market draws strength from the libertarian discourse elaborated since the 1970s by several winners of the Nobel Prize in Economic Sciences and adopted today in business papers like the Wall Street Journal. Its partisans say the U.S. Food and Drug Administration impedes innovation and access to medicines by making the evaluation process too long and costly.

Doug Sipp, a political science researcher at the Riken Institute in Japan, says that with regards to stem cell research, supporters of deregulation see "an opportunity to make their discourse heard and apply their theories."

The lack of reliable clinical data is only one of the serious ethical questions surrounding stem cell treatments. People with serious illnesses, as Turner points out, will go to desperate lengths to find a treatment. Which is "understandable," he adds. "But does that mean we should allow a market that profits from that despair and vulnerability?"

Read the original here:
The Shady Business Of Experimental Stem Cell Treatments - Worldcrunch