UCSD Researchers Win $18 Million Grant to Fund B-Cell Cancers Clinical Trial – Times of San Diego

Share This Article: Scanning electron micrograph of B lymphocyte. Image courtesy of National Cancer Institute.

The UC San Diego School of Medicine is receiving an $18.29 million grant to fund a clinical trial of a combination drug therapy to fight B-cell cancers, the university has announced.

The grant from the California Institute for Regenerative Medicine was approved Aug. 24.

The new combined drug trial, intended to study both safety and efficacy, is headed by Thomas Kipps, MD, PhD, Distinguished Professor of Medicine and deputy director of research at UC San Diego Moores Cancer Center, in collaboration with colleagues at the UC San Diego CIRM Alpha Stem Cell Clinic the cell therapy arm of the Sanford Stem Cell Clinical Center at UC San Diego Health.

The clincal trial combines an experimental antibody-based drug called cirmtuzumab with ibrutinib. Marketed as Imbruvica, ibrutinib is already approved to treat B-cell cancers, like chronic lymphocytic leukemia and mantle cell lymphoma. Cirmtuzumab is currently in clinical trials for the treatment of chronic lymphocytic leukemia.

We are very excited about evaluating this combination of targeted therapies in the clinic, Kipps said. Although ibrutinib has been approved for treatment of patients with CLL or MCL, it is exceptionally rare for this drug by itself to get rid of all the leukemia cells or cause long-lasting remissions without continuous therapy.

As a result, patients are recommended to take ibrutinib indefinitely until they develop intolerance or resistance to this drug, Kipps continued. By blocking a survival/growth-stimulating pathway that provides a lifeline to the leukemia cells of patients taking ibrutinib, cirmtuzumab can work together with ibrutinib to potentially kill all the leukemia cells, allowing patients to achieve a complete remission and stop therapy altogether.

Kipps noted, too, that cirmtuzumab targets cancer stem cells, which behave somewhat like the roots of the disease, resisting many forms of treatment and allowing a malignancy to grow back after apparently successful therapy. By targeting cancer stem cells, Kipps said cirmtuzumab may improve our capacity to achieve more complete and longer lasting remissions when used in combination with targeted drugs, such as ibrutinib, or other anti-cancer drugs for the treatment of patients with many different types of cancer.

The California Institute for Regenerative Medicinewas created in 2004 by California voters with $3 billion in funding support to accelerate stem cell research and treatments. Since 2004, UC San Diego researchers have received at least 96 CIRM awards, totaling more than $182 million.

Staff

UCSD Researchers Win $18 Million Grant to Fund B-Cell Cancers Clinical Trial was last modified: September 5th, 2017 by Toni McAllister

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UCSD Researchers Win $18 Million Grant to Fund B-Cell Cancers Clinical Trial - Times of San Diego

Ryan Custer, Elder grad injured at Oxford party, thanks community for their support – WCPO

CINCINNATI -- Ryan Custer tearfully thanked the community for their support at his prayer service Sunday.

I cant thank you guys enough, he said in front of a standing ovation at Elder High Schools Fieldhouse.

Custer, an Elder grad and Wright State freshman, suffered a traumatic spinal injury at a large party in April after he tried to jump into a shallow, makeshift pool.

Family and friends welcomed Custer home on Wednesday. He had been been recovering and undergoing therapy at University of Cincinnati Medical Center. He also traveled to Chicago to be considered for a stem cell study at Rush University.

Doctors injected 20 million stem cells into Custers neck, and HBO has been following his progress.

Ryans brother, Nick Custer, thanked the West Side community for being so uplifting to his family.

It means the world to us. It just shows you what a special kid Ryan is as a 19-year-old kid going through this, its just overwhelming support, he said.

Nick said Ryan will continue rehabilitation in Cincinnati, and he said Ryan is looking forward to the start of Wright States season.

Ryan wants to get back to the team as soon as possible, and they all want him to come back and help however he can. He misses them, definitely, Nick said.

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Ryan Custer, Elder grad injured at Oxford party, thanks community for their support - WCPO

Stem Cells and "Mishandling" Smallpox – Liberty Nation – Liberty Nation (registration) (blog)

GABRIELLA FIORINO

We trust our doctors with our lives. However, what is the reaction when some medical professionals allow unsanitary measures and diseases to break out into the population? Four institutions in the U.S. came under fire recently by the FDA for improperly handling microbiological organisms and exposing the public to smallpox after conducting unapproved techniques, endangering hundreds of lives.

The FDA identified four medical centers in California and Florida as utilizing unapproved stem cell therapies for those with cancer and other serious illnesses. One of the institutes, California Stem Cell Treatment Centers, applied a method developed by StemImmune Inc., which consisted of injecting clients with a mixture of the smallpox vaccine and stem cells. Dr. Mark Berman, co-founder of the California center, described their methods as cutting edge therapy for stage-4 cancer patients, as reported by the Los Angeles Times.

The consequences of such methods are worrisome; as the FDA claims exposure to the smallpox vaccine significantly increases the risk of life-threatening complications, including heart inflammation. Perhaps even more troubling is the fact that individuals in contact with those receiving the vaccine may develop similar symptoms, possibly infecting hundreds of others. The FDA is currently investigating how StemImmune Inc. received shipments of the vaccine, as the product is unavailable on the market.

The Stem Cell Clinic of Sunrise, Florida is another facility under investigation by the FDA for taking improper sanitary measures to prevent contamination during their therapies. According to the agency, the clinic refused to permit entry of an FDA inspector without an appointment, which is a violation of federal law. This refusal would not be the first time the Florida institution came under fire. According to the New England Journal of Medicine, three clients suffering from macular degeneration sustained blindness following treatment at the facility.

A variety of sources derive stem cells, including bone marrow, blood, umbilical cords, and controversially, human embryos. These products aid in the development and restoration of healthy human tissue, and help battle cancer, heart disease, and Parkinsons disease, as noted by the University of Utah. These products are also employed for spinal cord injuries, indicating critical applications, as the central nervous system does not naturally permit neuro-regeneration following damage. Excitingly, organs growth for those requiring life-saving transplants is another possible advancement.

These innovations are not without consequences, however. According to the Mayo Clinic, some may develop graft-versus-host disease, a condition in which a donors stem cells attack the patients tissues and organs, possibly leading to death. Risks of brain tumor development are also an increased possibility for those receiving injections in the spinal cord, as abnormal tissue growth may result.

As the FDA investigates unsound practices by the four institutes endangering the lives of hundreds, Americans should not be misled regarding stem cell therapies. Through proper sanitary measures, their uses are a huge medical development, comprising a myriad of medical advantages. Liberty Nation will keep readers up to date regarding the actions of the FDA against the four clinics.

Gabi is a Biomedical Sciences major and manages a Cognitive Neuroscience Research Lab at the University of Central Florida. A Libertarian, Gabi says shes surrounded on by whiny, wannabe anti-capitalists, posting about their victimhood on Facebook.Although leftists often confuse her with privileged white girls, Gabi is Puerto Rican and Italian.Make sense of that, liberals!

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Stem Cells and "Mishandling" Smallpox - Liberty Nation - Liberty Nation (registration) (blog)

Family hope to raise 160k for groundbreaking stem cell treatment for daughter, Ivy, who suffers from cerebral palsy – Scottish Daily Record

Little Ivy Rose has a smile that lights up a room but unless her parents raise enough money for groundbreaking treatment she will have to use a wheelchair for the rest of her life.

The three-year-old faces a life of isolation because her cerebral palsy means she can do very little for herself. But she is a delightfully engaging child who shows courage beyond her years.

Stephen and Sky Summers, from Shotts, Lanarkshire, were devastated when their little girl was born prematurely with medical difficulties.

Ivy was born just a year after the couples twins, Xander and Sandy died after being born too prematurely.

Sky, 36, said: They died in my arms. One was just under an hour, the other just over an hour.

When Ivy also arrived early her parents feared she would die too.

Now they are determined to do everything within their power to ensure she gets the very best chance to live as normal a life as possible.

Sky said: When Ivy arrived, she was whisked off to ICU. I didnt even get to touch her. We didnt think there were going to be big problems at first. She came out crying and gurgling.

Initially, Ivy was tube fed and it was three weeks before she could have milk from a bottle. Her problems didnt become completely apparent until Ivy came home at five weeks.

Sky said: We brought Ivy home and within the first 24-48 hours, she had what we call her first episode.

She stopped breathing. She was sleeping in the carrycot next to our bed. I fed her, put her into carrycot, turned round and heard a commotion.

Her arms were shaking and she was very distressed. She couldnt breathe. I picked her up put her across my knee, patting her back but I couldnt get her to start breathing. She started turning blue.

It was a terrifying moment. I started to very gently breathe into her mouth and she came round and started breathing again.

That was the beginning of many episodes over the next eight months. It was a very traumatic time where we just tried to keep her alive.

It transpired the tot had acid reflux and the pain and shock of the acid was enough to stop her breathing.

As she grew, her condition improved but Ivy has never been able to eat anything other than mushy food because of her cerebral palsy.

She is a happy, bright little girl but her mum is not prepared to accept there is no hope of any improvement.

Sky said: Ivy sees NHS specialists but they are only interested in managing her condition, not in curing or rehabilitating it.

When the cerebral palsy diagnosis came through around her second birthday, Sky said: I felt hopeless.

I remember very specifically being told the likely scenario was Ivy would never be able to walk unaided but she would maybe be able to manage around the house, holding on to furniture. She would most likely be in a wheelchair. The best hope is for Ivy to start any therapies as soon as possible because once she is seven her ability to be improve her mobility will diminish.

A connection through family led to meeting Dr Joanne Kurtzberg, who is awaiting approval from the US Food and Drug Administration for stem cell treatment with donor cells on cerebral palsy patients. Kurtzberg has agreed to accept Ivy on to the trial if she meets the criteria.

Ivy also has the opportunity to have treatment from specialists RehabMart including sensory therapies involving work with horses, special suits and trapezes among others.

While some of the therapies will be free, many others are expensive.

The family will have to live in the US for six months to give Ivy her best chance of improvement but it will cost 162,000 which they are hoping to crowdfund.

Sky said: It is a once-in-a-lifetime opportunity for Ivy. I am so blessed she is so happy, so affectionate, intelligent and funny but she is excluded from everywhere in life.

Exclusion is a horrendous part for a child with cerebral palsy.

Cerebral palsy is the name for a group of lifelong conditions which affect movement and co-ordination, caused by a problem with the brain which occurs before, during or soon after birth.

The symptoms arent usually obvious just after a baby is born. They become noticeable during the first two or three years. It affects each person differently but the condition may limit a childs activities and independence.

The problem with the brain doesnt worsen but the condition can put a lot of strain on the body.

To donate, go to: http://www.justgiving.com/crowdfunding/ivyrosesummers .

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Family hope to raise 160k for groundbreaking stem cell treatment for daughter, Ivy, who suffers from cerebral palsy - Scottish Daily Record

Stem Cell Therapy and Its Revolutionary Purposes Guardian … – Guardian Liberty Voice

Stem cell therapy is reaching another stage in the healthcare world by offering hope through revolutionary solutions to complex diseases. However, with progress come controversy.

Part of the debate lies in the disbelief stem cell therapy is as revolutionary asresearchers claim. The forerunners of this therapy want to replace the current treatment of Alzheimers, and cancer. There are even biotech scientists who claim experiments have shown promisebringing thebrain dead back to life, although, nothing concrete has been published.

Supporting scientists of the therapy have solid evidence thatevery disease originatesin specific cells. It is key to work with cells to find a potential cure for any illness. The first cell of a human is the stem cell; a pluripotent cell is a component of life and capable of replicating any other cell in the body. In fact, every cell in the human body comes from this cell. Pluripotent cellsare found in embryos or created from other cells making the process expensive.

With a cell capable of transforming into others, lab developers hope to find simple solutions to complexproblems. Alzheimers disease is the deteriorationof the brain cells (neurons), causingthem to die. Scientists can reverse thisby administrating stem cells into the brain to create new neurons, according to stem cell therapy supporters.

The Food and Drug Administration (FDA) is becoming the fiercest enemy of stem cell therapy. Recently, theagency sanctioned clinics that useunapproved therapies. They seizedvials of the smallpox vaccinefrom some clinics. The FDA attacked them for not having enough proof of their practices. Somehow, the FDA is right to think this way because of the public silence of the therapys developers. People need more information about the treatment and general development.

The medical gesture of health and procedures, as well asdiagnosis, is based on scientific and proven knowledge. Contrary to the aforementioned therapy, there is a long list of publishing in medicine. It is certain that there are professionals working on stem cells, but the mistrust is justified.

Whether the therapy is legit, trustworthy, or efficient, ithas a bright future. The need forlargeamounts of money to fund theproject is undeniable. Big relevant companies, such as CSL Behringare investing moneyto accelerate the growth of the therapy.

A new groundbreaking technique is being tested that couldbring brain dead patients back to life. People who cannot live without a machine. Specialists say it is impossible to reverse that kind of damage, but stem cells therapy offersa new alternative.

People notice how much power the stem cell industry has right now. Even if individualsdo not have the legal backing, they enjoy the advocacy of powerful individuals. It is sane to remember that the major scientific progress made in history was due to experimentation. Is better if it sounds impossible to accomplishbecause it can prove the human greatness to fight against something as natural as death.

Opinion News by Gian Torres Edited Jeanette Smith

Sources:

CBS NEWS:FDA cracks down on clinics selling unapproved stem cell therapies BioPharma:CSL adding scalable stem cell gene therapy tech in $91m Calimmune buy Wall Street Pit:Brain Dead Patients Could Be Brought Back to Life in Groundbreaking Stem Cell Therapy

Featured and Top Image Courtesy of Berkshire Community College Open Bioscience Image Librarys Flickr Page Creative Commons License

alzheimers, FDA, spot, stem cell, Stem-cell Therapy, treatments

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South Bend man a ‘walking miracle’ after cancer treatment breakthrough – South Bend Tribune

Video: CAR T treatment gives hope in cancer fight

In CAR T-cell therapy, a type of white blood cell called T-cells are extracted from the patients blood and modified in the lab to recognize specific cancer cells. These supercharged T-cells are then infused back into the patient, where they search out and destroy cancer cells.

The therapy, often described as a living drug because it is customized with each patients T-cells, will be marketed as Kymriah by Swiss pharmaceutical maker Novartis.

Scott was excited to hear news Wednesday that the FDA approved the same treatment for a form of childhood leukemia, meaning, he hopes, that it won't be long before it's approved for his form of cancer, diffuse large B-cell lymphoma. The FDA called the approval "historic" because it marks the first cell-based gene therapy approved in the United States.

Scott is one of 130 patients nationally in the clinical trial for his form of lymphoma, and he was the first to receive the treatment at UCM. That happened in May 2016, when he had exhausted all other options.

Scott has been feeling good for just less than a year. Chemotherapy has taken his hair three times but he has a full head of it once again. He can play an entire round of golf with his son. An avid Notre Dame football fan and season ticket holder, he had to miss each game in 2015, but plans to attend every game this season.

In May 2013, Scott noticed a painful growth in his groin area. His family doctor, Dr. Joseph Caruso, said he had developed a swollen lymph node, which could have resulted from his body trying to fight off an infection. Caruso asked him if he had recently had an infection, and Scott recounted recently stepping on a rusty nail while the roof on his home was being replaced. Caruso prescribed an antibiotic and the swelling seemed to go away.

But four months later, while in the shower, Scott noticed another lump under his arm. He went back to Caruso, who referred him to South Bend-based Beacon Health System oncologist Dr. Thomas Reid. After some scans, Reid diagnosed Stage 3 lymphoma.

Reid administered the standard treatment, four cycles of a chemotherapy regimen known as R-CHOP, an effective but highly toxic blend of drugs causing severe side effects. The fourth cycle had to be delayed because he developed appendicitis, and it was tougher than the first three.

After all of that, the cancer started growing again just two months later.

Reid referred him to Dr. Sonali Smith, professor of medicine and director of UCMs lymphoma program. Smith and her team knew the CAR T-cell therapy was being investigated in a few select centers. Their short-term goal was to keep him alive until they could be cleared to administer the clinical trial.

In February 2015, Scott received a stem-cell transplant, which went smoothly. But three months later, the cancer again started growing. Participation in two more clinical trials and some precisely targeted radiation therapy bought a little more time, but by late 2015, his lymphoma was gaining on him.

Then, in early February 2016, the UCM team received the go-ahead for the CAR T-cell treatment and began harvesting his T cells, a process that resembles dialysis. Scott said another patient had been slated to receive the treatment first, but that patient died.

It was during an appointment in May 2016, just a week before the treatment, that Scott first grasped how close he was to dying. Smith told him the treatment could cause severe side effects, including death. Five people in the trial had died.

I said, I understand. What other options do I have? Scott recalled. She says, Oh youve already surpassed all expectations. I said, What do you mean by that? And thats when she said, after the stem cell, if it comes back, life expectancy is six months. It was a rough day. On the way home I was pretty shaken up.

A little after 9:30 a.m. on May 18, 2016, Scott, sporting a Notre Dame baseball cap, was prepared for the treatment. Carefully observing was Dr. Michael Bishop, professor of medicine and director of the Hematopoietic Cellular Therapy Program at UCM, and about a dozen members of his team. A technician brought in his modified T-cells, thawed them out and infused them into Scott intravenously.

Ten minutes later, the treatment was finished. Afterward, he and his wife Cindy spent 28 days in the hospital and then were required to live in an apartment within 10 minutes of the university hospital. They were allowed to move back home to South Bend in July, about two months after the treatment.

Its incredible, Cindy said of Scotts recovery thus far. We did not realize what we were getting into, all of the risks, until days before. She (Dr. Smith) may have mentioned it but it didnt sink in. We both realized that win, lose or draw, theyre going to learn so much, just from how he responds to it.

Cindy praised how well Drs. Reid and Smith worked together between South Bend and Chicago, and how they told them just enough to be informed without telling them so much that they panicked.

She said, theres this trial, Cindy said. This is for you. You were designed for this trial and it was designed for you. We just have to keep you going until we can give it to you.

The treatment was on a Wednesday. By Friday night, his first fever came and it wasnt a surprise. Once they enter the body, each T cell multiplies rapidly, producing thousands of offspring. Then they launch a vigorous assault. All of that warfare occurring inside the body can cause severe flu-like symptoms: fever, swelling, low blood pressure.

On Sunday his fever spiked to 104 degrees. They packed him in ice around his neck and under his arms, and managed to break the fever without sending him into intensive care.

He also experienced some neurological effects, including tremors, cognitive delays and blurred vision.

Now, more than a year later, Smith still wants to see Scott every three months, and he remains very susceptible to infections because his immunity will always be compromised not from the CAR T-cell but from all of the chemotherapy. He still has some swelling because the scar tissue from three surgeries restricts the flow of lymphotic fluids.

I feel it all the time and I have very limited range of movements but it doesnt stop me, he said.

Unless the lawn needs to be mowed, then it really bothers him, she said. Some things will never change.

She said she never imagined she had married a pioneer.

I knew I had married somebody very unique, very special, but definitely not a pioneer, she said. He was the last person you ever thought would be sick. Doesnt drink. Doesnt smoke. Never had ventured on the wild side. This wasnt supposed to happen.

So far the FDA has only approved T-cell treatments for blood cancers, such as lymphoma and leukemia, but not solid tumor cancers, such as breast and colon cancer, which kill many more people. But Bishop of UCM said that day is coming. He expects those clinical trials to begin within a year or two, and receive FDA approval within about five years.

Its very exciting, Bishop said. The technology is a little more complicated but it has the potential to treat a broad spectrum of cancers. Ive been doing this for 25 years and this is one of the most significant advances Ive seen in my career.

Meanwhile, Scott will keep telling his story of hope to everyone he can, including himself. Bishop said Scott's cancer has a 10- to 20-percent chance to recur.

Youre still thinking that the other shoe can drop, Scott said. The mantra I use when negative thoughts enter my head is, Alright Scott, are you giving up? No. Are you quitting? No. Then shut up. I dont know if that will ever go away.

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South Bend man a 'walking miracle' after cancer treatment breakthrough - South Bend Tribune

FDA announces first US gene therapy approval for cancer treatment – kfor.com

The US Food and Drug Administration approved a new leukemia treatment, which the agency considers the first gene therapy it has cleared to hit the market in the United States.

The treatment, called Kymriah, aims to give some patients a second chance after first-line drugs have failed. This may happen in up to a fifth of patients, according to the FDA.

Each dose of Kymriah contains a patients own immune cells, which are sent to a lab to be genetically modified using a virus. The therapy known as chimeric antigen receptor T-cell therapy, or CAR-T gives the cells the ability to recognize and kill the source of the cancer.

Were entering a new frontier in medical innovation with the ability to reprogram a patients own cells to attack a deadly cancer, said FDA Commissioner Dr. Scott Gottlieb ina statement.

Weve never seen anything like this before, and I believe this therapy may become the new standard of care for this patient population, said Dr. Stephan Grupp, director of cancer immunotherapy at Childrens Hospital of Philadelphia, which spearheaded this research.

An FDA advisory committee hadrecommended the therapyfor approval in July to treat the relapse of a blood cancer known as B-cell acute lymphoblastic leukemia, or ALL.

Based on available data, patients on the treatment have had an 89 percent chance of surviving at least six months and a 79 percent chance of surviving at least a year, with most being relapse-free at that point.

Almost 5,000 people were diagnosed with ALL in 2014, according to the US Centers for Disease Control and Prevention. More than half were children and teens. ALL is the most common type of cancer among children, according to the National Cancer Institute.

Most patients with ALL recover through other treatments such as radiation, chemotherapy and stem cells. But, if the cancer recurs, the prognosis is poor.

There has been an urgent need for novel treatment options that improve outcomes for patients with relapsed or refractory B-cell precursor ALL, said Novartis, the drug company that makes Kymriah, in a statement.

Kymriah is a first-of-its-kind treatment approach that fills an important unmet need for children and young adults with this serious disease, said Dr. Peter Marks, director of the FDAs Center for Biologics Evaluation and Research, in a statement.

The one-time treatment has a boxed warning for cytokine release syndrome or CRS, a life-threatening side effect that can cause blood pressure to drop dangerously low. It is caused by overactive genetically modified immune cells. The FDA said hospitals and clinics must become certified to distribute the treatment, meaning they are prepared to recognize and treat CRS and other potentially fatal neurological events. Novartis said it hopes to have an initial network of 20 treatment centers within a month with plans to expand that to 32 by the end of the year.

Kymriah has a $475,000 price tag, however patients who do not respond within a month of treatment will not be charged, according to Novartis.

Novartis is collaborating with (Centers for Medicaid Services) to make an outcomes-based approach available to allow for payment only when pediatric and young adult ALL patients respond to Kymriah by the end of the first month. Future potential indications would be reviewed for the most relevant outcomes-based approach, the drug company said in a statement.

On Wednesday, the FDA also expanded approval for another drug, tocilizumab, to treat CRS in patients 2 and older.

In the main studythat informed the advisory committees decision in July, roughly half of 68 patients experienced high-grade CRS, though none died from it. Slightly fewer patients experiencedneurological events, such as seizures and hallucinations.

Novartis is required to conduct followup study to assess the safety of the treatment long-term.

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FDA announces first US gene therapy approval for cancer treatment - kfor.com

Stem Cell Market Analysis 2022: Latest Trends, Top Manufactures and Business Opportunities – satPRnews (press release)

In this report, the global Stem Cells market is valued at USD XX million in 2016 and is expected to reach USD XX million by the end of 2022, growing at a CAGR of XX% between 2016 and 2022.

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The Stem Cell market report includes a comprehensive analysis of the present state of the market. The report starts with the basic Stem Cell industry overview and then goes into each and every detail.

Access Stem Cell Market Report at: https://www.marketreportsworld.com/10383969

The Stem Cell market overview, which is the beginning of the report consists of various factors such as definitions, applications, and classifications of the Stem Cell. Industry chain structure, industry news analysis, and industry policy analysis are also covered in the industry overview section of the market research report.

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In-depth analysis of the company profiles and competitive strategies offered in the Stem Cell market research report

Top Manufacturers Mentioned In Stem Cell Market report are:CCBC, Vcanbio, Boyalife, Beikebiotech and more.

Regions covered in theStem Cell Market report include:North America, China,Europe,Japan,India and Southeast Asia.

Further in the Plasmid Sales Market research report, following pointsProduction, Sales and Revenue, Supply and Consumption and other analysisare included along with in-depth research. Stem Cell Market Product Types include: Umbilical Cord Blood Stem Cell, Embryonic Stem Cell, Adult Stem Cell along with Applications that include: Diseases Therapy, Healthcare

Get Stem Cell Market Purchase Report at: https://www.marketreportsworld.com/purchase/10383969

The Stem Cell industry research report analyses the supply, sales, production, and market status comprehensively. Production market shares and sales market shares are analysed along with the study of capacity, production, sales, and revenue. Several other factors such as import, export, gross margin, price, cost, and consumption are also analysed under the section Analysis of Stem Cell production, supply, sales and market status.

In the end, Stem Cell market report is a treasured source for both the individuals as well as the businesses as it provides detailed SWOT analysis along with the new project investments feasibility study.

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Stem Cell Market Analysis 2022: Latest Trends, Top Manufactures and Business Opportunities - satPRnews (press release)

Landmark stem cell paper questioned – BioEdge

Oh no! Not again! Such must be the sentiments of stem cell scientists after a paper to be published in Nature cast cold water on landmark research about editing the genome of a human embryo.

On August 2, a team led by Shoukhrat Mitalipov, of Oregon Health and Science University, announced in Nature that they had successfully deleted a disease-causing faulty gene and replaced it with a healthy copy using the CRISPR-Cas9 technique. Their innovative experiment introduced the CRISPR machinery earlier. When they examined the embryos, they found that they did not contain the faulty sequence.

This discovery was greeted around the world as a first step towards freeing mankind from genetic disorders or towards a eugenicist society, depending on your attitude towards modifying the human genome. Technically, it was a tour de force, as it was relatively easy and accurate and did not result in mosaic embryos.

With 10,000 harmful single-gene mutations known, there is a lot at stake.

However, a closer examination of the exciting paper has sparked a lot of debate amongst stem cell scientists. In a preprint release of a paper in Nature on bioRxiv, Dieter Egli, of Columbia University, and Maria Jasin, of Memorial Sloan Kettering Cancer Center, along with Harvard geneticist George Church, have questioned whether Mitalipovs team has actually succeeded, as the new technique contradicts the conventional wisdom about how fertilisation occurs. They point out that although the disease-causing gene had disappeared, there was no proof that the correct sequence had been inserted.

Furthermore, the DNA from the sperm and the egg are probably not close enough in the brief interval after fertilisation to interact or share genes. Mitalipov and his team had speculated that the embryos used the DNA of the egg as a guide to repair the mutation carried by the sperm.

In my view Egli et al. convincingly provided a series of compelling arguments explaining that the correction of the deleterious mutation by self repair is unlikely to have occurred, Gatan Burgio, a geneticist at the Australian National University told Nature News.

Mitalipov has responded, promising to answer the critiques point by point in the form of a formal peer-reviewed response in a matter of weeks.

Inevitably, this latest breakthrough recalls a string of too-good-to-be true-and too-amazing-to-reject articles about stem cell research. They were published in leading journals, hyped in the media and then crashed and burned. Time will tell whether Mitalipovs paper will be vindicated.

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Landmark stem cell paper questioned - BioEdge

UNMC research traces glaucoma, often associated with aging, to earliest days of development – Omaha World-Herald

Glaucoma is known as a disease of aging, the kind that creeps up on people and slowly robs them of vision. But a researcher at the University of Nebraska Medical Center has traced the roots of a common form of the eye disease to a much earlier time, literally the earliest days of human growth and development.

The discovery, published recently in the journal Stem Cells, may offer opportunities for earlier diagnosis of the disease as well as new treatment options.

Iqbal Ahmad, a professor in the ophthalmology and visual sciences department at UNMC, said there are several forms of glaucoma, which ranks as the second-leading cause of blindness and affects approximately 3 million people in the United States and some 60 million worldwide.

All forms, said Ahmad, who led the team of researchers, have one thing in common: Cells inside the eye known as retinal ganglion cells, which extend from the retina and give rise to the optic nerve, begin to degenerate. The optic nerve carries visual messages from the eye to the brain.

The condition typically comes on with little notice and few symptoms, creeping up so slowly that patients often dont notice until their optic nerve is compromised and, with it, their vision. The loss begins on the periphery. Many unconsciously compensate by turning their heads.

Thats why they call it the silent robber of vision, Ahmad said.

High pressure inside the eye is a risk factor for glaucoma, he said. But in some cases, patients with normal eye pressures suffer optic nerve degeneration. Such cases were one of the factors that led Ahmad and his team to look to the early days of development.

Ahmad said the team hypothesized that the retinal ganglion cells, which form during gestation, were somehow vulnerable or even flawed from the start in those who develop glaucoma.

To study them, however, they had to go back to those early stages of development. So the researchers took blood from adults with primary open angle glaucoma, which affects 90 percent of glaucoma patients, and reprogrammed the blood cells back into an earlier state, known as induced pluripotent stem cells. Such cells, by definition, have the potential to differentiate into a number of different cell types, from bone to heart, with the right programming.

The team figured out how to make them differentiate into retinal ganglion cells in an unlimited supply they could use for research. Pooja Teotia, a post-doctoral scholar in Ahmads lab, played a crucial role in the work.

The stem cell model was based on a gene variation known to be associated with primary open angle glaucoma. About 40 percent of Caucasians have at least one copy, said Dr. Shane Havens, a glaucoma specialist at UNMCs Truhlsen Institute who is familiar with Ahmads work. More than 99 percent of people of African descent have it, which partially explains why African-Americans have higher rates of glaucoma.

Ahmad stressed that the process did not involve the use of embryonic stem cells. Research based on embryonic cell lines has been controversial because the original cells were derived from human embryos. The ethical dilemma we used to face has been circumvented, he said.

The researchers then compared the retinal ganglion cells derived from the glaucoma patients blood with those from a healthy adult who didnt have glaucoma. The glaucoma patient-derived cells differed in form, function and gene expression.

They even looked different, Ahmad said. The nerves that came out of the young retinal ganglion cells looked much weaker and smaller than the normal retinal ganglion cells. At the functional level, they were not behaving normally.

Ahmad said the team is excited about the next steps. Being able to study the abnormal cells in a dish is giving the researchers an amazing amount of information about what might have gone wrong at the molecular level as well as along the intricate signaling pathways in their development.

Both offer the potential for earlier diagnosis and for new treatments. Ideally they would be able to identify patients who might develop the disease decades down the road and treat them before degeneration occurs.

Havens said treatments for glaucoma currently involve lowering eye pressure with medication, lasers or surgery. But that often comes after people have lost a significant portion of the optic nerve.

About 2 percent of people in the United States have glaucoma, but about half of them dont know it.

This would allow us to start earlier in patients who are at risk, he said.

Ahmad said the researchers also are working to see whether they can correct abnormalities in the cells and to determine whether they would find their way and connect with the brain. If that works they may be able to transplant them into patients who already have the disease and reverse the degeneration.

Were seeing some encouraging signs, he said.

Havens said the work, particularly the stem cell technique involved, also has broader implications for the study and treatment of other diseases, such as Parkinsons disease, that involve the nervous system.

Its exciting work, for sure, he said.

julie.anderson@owh.com, 402-444-1066

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The only sure way to diagnose glaucoma, according to the American Academy of Ophthalmology, is with a complete eye exam. A glaucoma screening that checks only eye pressure is not enough to find glaucoma.

So when should someone have an eye exam? According to the group, adults with no signs or risk factors for eye disease should have a comprehensive medical eye evaluation at age 40, if they havent had one already. After age 40, the recommended interval is:

Age 40 to 55, every two to four years

Age 55 to 64, every one to three years

Age 65 and older, every one to two years

For those at higher risk of certain diseases, including African-Americans and Hispanics who are at higher risk for glaucoma, comprehensive eye exams should be considered:

Under age 40, every two to four years

Age 40 to 54, every one to three years

Age 55 to 64, every one to two years

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UNMC research traces glaucoma, often associated with aging, to earliest days of development - Omaha World-Herald