Author Archives: admin


Trump’s travel restrictions will hurt cell therapy sector says ISCT – In-PharmaTechnologist.com

If reinstated, Donald Trumps order restricting travel to the US would hurt the cell therapy sector according to the International Society for Cellular Therapy (ISCT).

US President Donald Trump issued an executive order on January 27 that limited immigration from seven predominantly Muslim countries, halted refugee admission for 120 days, and barred all Syrian refugees.

Last Friday , a judge in Seattle suspended implementation of the order after lawyers representing Washington and Minnesota argued it was unconstitutional and discriminatory.

In response, Trump criticized the presiding judge and vowed to have the order reinstated. However, at the time of writing, nothing has been decided.

If reinstated, the travel restrictions will negatively impact the cell therapy sector according to the International Society for Cellular Therapy (ISCT) a Canada-based group representing doctors, regulators, researchers and industry which raised concerns in a statement today.

The US plays an essential part in cell therapy research as a leading country in the life science industry. It hosts the highest number of international conferences, critical for scientific collaboration and sharing of ideas.

The ISCT also highlighted the leading roles US investors and the FDA play in shaping the global cell therapy sector and warned against any regulations that restrict international collaboration.

ISCT views any policies that would prevent the free movement of properly credentialed scientists, patients, care givers and/or their families from entering the US, as significantly harmful to the sharing of key scientific findings and the ability to deliver cell therapy to all patients.

ISCT President Catherine Bollard told us The Executive Order may result in a loss of talented researchers being able to come and work in the US to develop cell therapeutics given how much the US relies on foreign talent in the research and development sector.

She also suggested that some researchers returning to their country of origin because they do not feel comfortable continuing to live in the US.

Bollard confirmed that ISCT has one member from a country covered by the executive order.

View post:
Trump's travel restrictions will hurt cell therapy sector says ISCT - In-PharmaTechnologist.com

British Synbio’s Llama Antibodies recruited for Cancer T-Cell Therapy – Labiotech.eu (blog)

Isogenica has licensed its synthetic llama antibody library to Maverick Therapeutics, which develops cancer T-cell therapies designed to reduce side effects.

Isogenica is a synthetic biology company near Cambridge that develops libraries of therapeutic antibodies. The biotech has granted US-based Maverick Therapeutics licenses to its llamdA VHHantibody library for the discovery, development and commercialization of therapeutic products. In exchange, it will receive upfront, annual and milestone payments as the antibodies are developed by the client.

Isogenicas llamdA VHH library comprisessingle domain llama antibodies created and screened in vitro,which consumes half the time and creates greater diversity than immunizing llamas. According to the company, its llamdA system routinely interrogates the equivalent to the whole antibody repertoire of one million llamas.

Maverick Therapeutics is a very young biotech, spun out from Harpoon Therapeuticsjust last year. The company is backed by MPM Capital, a USVC managed by biotech veteran Patrick Bauerle from Munich.

The company is developing a unique approach to T-cell cancer therapy. Its antibodies are designed to be inactive when administered and only activate in the tumor microenvironment. This way, theT-cells do not attack healthy tissues, avoiding side effects. Japanese big pharma Takeda recently offered the young company 117M ($125M) to develop this technology.

Mavericks approach looks promising since severe side effects are common in T-cell therapies such asCAR-T, with some companies reporting thedeathof several patients. Other companieslike the French Cellectis and Stimunity are also developing their own strategies to increase the safety of CAR-T.

If successful, the development of Isogenicas antibodies by Maverick could bring the British biotech revenues to accelerate the launch of its new library of fully synthetic human antibodies.

Images from Sergey Didenko /Shutterstock

View post:
British Synbio's Llama Antibodies recruited for Cancer T-Cell Therapy - Labiotech.eu (blog)

Clinic claims it has used stem cells to treat Down’s syndrome | New … – New Scientist

Downs: an extra chromosome 21

Department of Clinical Cytogenetics, Addenbrookes Hospital/Science Photo Library

By Andy Coghlan

A CLINIC claims it has used stem cells to treat Downs syndrome in up to 14 people. As far as we know, its the first time that stem cells have been used to treat Downs syndrome, says Jyoti Titus, manager at Nutech Mediworld clinic in New Delhi, India.

The announcement has set alarm bells ringing. Its not clear to independent stem cell or Downs experts how stem cells which can form many types of tissue might treat Downs, a genetic disorder caused by having an extra chromosome. The use of these cells does not make biological sense and may place the babies at considerable risk of side effects,says John Rasko of the International Society for Cellular Therapy.

Clinically proven stem cell therapies are only just starting to become available. The first off-the-shelf stem cell treatment to gain regulatory approval was launched in Japan last year, and prevents transplanted organs from attacking their recipients. A number of research teams are putting other experimental stem cell therapies through stringent clinical trials.

But hundreds of clinics worldwide already offer stem cell treatments unvetted by regulatory authorities. A patent held by the clinics medical director, Geeta Shroff, from 2007 suggests that the cells offered by Nutech Mediworld could be helpful for over 70 types of conditions, from Downs syndrome to Alzheimers disease, and even vegetative states.

The use of stem cells doesnt make sense and may place the babies at considerable risk

Most treatments for children with Downs syndrome centre on support including speech and behavioural therapies. But in a study published last year Shroff, reported that a baby with Downs syndrome developed better understanding, improved limb muscle tone, and the ability to recognise his relatives after receiving stem cells (Journal of Medical Cases, doi.org/bx3v).

Theres no comparison to similar individuals with Downs syndrome, and no indication this therapy had any effect whatsoever, so the author has no basis at all for saying the injections were beneficial, says Elizabeth Fisher at University College London.

But since no other treatment was given, it is evident that the childs improvements were due to stem cell treatment, says Titus. He started babbling and crawling, and his facial features underwent a change. The boy, who lives in Singapore, is now 3 years old. He continues to develop age-appropriate skills, says Titus.

Shroffs study says she injected the cells, developed from a donated embryo, into his blood, back muscles and under his skin, as well as giving them as a nasal spray. Stem cells have an innate ability to repair and regenerate, and that is how the babys condition improved, says Titus.

Theres no obvious way in which this treatment would have worked, says Victor Tybulewicz at the Francis Crick Institute in London. To have any effect, neural stem cells would need to be injected into the brain, he says.

The author appears to have no idea of where [the cells] are going, or what theyre doing, says Fisher. Its even worse now we know theyve treated 14 patients, not just one.

Titus says that the way the cells were developed means recipients dont need immunosuppressants. But Tybulewicz disagrees. I expect the most likely outcome of the injections would have been that they were recognised as foreign and eliminated by the immune system, he says. More details of the biological impact of the stem cells will be revealed in a study that has been submitted for publication, says Titus.

Nutech Mediworld isnt the only clinic offering stem cells. An analysis led by Rasko last year identified 417 unique websites advertising stem cell treatments directly to patients. Of these, 187 were linked to 215 clinics in the US. Thirty-five websites were linked to organisations in India.

Although India introduced national guidelines on clinical stem cell research and treatments a decade ago, these are not legally binding.

This article appeared in print under the headline Clinic claims stem cells treat Downs syndrome

More on these topics:

View original post here:
Clinic claims it has used stem cells to treat Down's syndrome | New ... - New Scientist

‘Stem cells grew me a new heart’ says Gordon Foster after treatment … – Hull Daily Mail

An East Yorkshire dad who missed out on a heart transplant by just one per cent has become the first patient in Europe to undergo revolutionary treatment on compassionate grounds.

Gordon Foster suffered his first heart attack at 30 and went on to have two major and several smaller heart attacks which caused severe damage to his heart muscle.

Yet, despite his heart working at only 17 per cent of its normal function, he missed out on a heart transplant because it was just above the threshold of 16 per cent.

Now, Gordon has become the first patient to undergo stem cell treatment to regenerate part of his dead heart muscle through the new Compassionate Treatment Programme, the first of its kind in Europe, at the world-famous St Bartholomew's Hospital in London.

Read more: Migraines change Hull mum's accent into Scouse, Geordie and Irish

At his home in the hamlet of Thornholme near Bridlington, Gordon, 59, said: "I thought last year would be my last. Now, I have so much hope for the future.

"I have had the best care I could ever wish for from the NHS. I can't believe how lucky I've been. Someone up there must be looking out for me."

Gordon developed cancer when he was 22 and believes his illness may have been linked to his father's work for the RAF testing British nuclear weapons in Christmas Island in the 1950s. Around 21,000 British servicemen were exposed to explosions wearing no protective clothing and dressed in khaki desert fatigues.

He said: "I remember as a child, the radio used to crackle when my dad walked past and when he died, he was riddled with cancer."

Gordon underwent intensive radiotherapy which may have damaged his heart and suffered the major heart attack eight years later as he renovated his home for him and his bride-to-be Joanne. The couple brought forward their wedding day in case he did not survive.

However, they went on to have two children James, now 25, and Rebekah, 23, but Mr Foster's health declined over the years despite him throwing himself into his job as a welder fabricator for structural steel firm Severfield Reeve.

"I worked in heavy industry, handing upside down off beams welding, and I was putting in 110-hour weeks, often away from home for seven weeks at a time," he said.

More news: Nurses quit after 138m NHS contract is awarded to health care company

"I just got it into my heard that I had to prove to people that I wasn't on the scrap heap and threw myself into work. With hindsight, it was the wrong thing to do."

After experiencing more heart attacks and being told by a cardiology specialist he needed a heart transplant, Gordon went to Papworth Hospital in Cambridgeshire. Tests showed his heart function rate was 17 per cent, just one per cent too high for a heart transplant.

He said: "It was a very humbling experience. I thought I had it bad but when I saw some of the other patients, it was unbelievable how sick they were.

"I thought they were far more deserving than me and I would have felt guilty if they had put me on the transplant list."

So, Gordon soldiered on, his health deteriorating by the day. And he sank into a deep depression as his life became more restrictive. Despite his employers changing his role several times in an attempt to reduce his workload, he had to give up work on medical grounds about 10 years ago.

At home, a stair lift was fitted and his home was adapted because he ended up with terrible pains in his chest and on his knees by the time he reached the top of the stairs.

Five years ago, Gordon was invited to take part in a Stem Cell Research Trial, funded by the Heart Cells Foundation, to help patients with heart failure. However, he was selected at random as part of the group receiving a placebo so his condition did not improve.

More news: Government accused of smoke screen over 'health tourism' plan

However, in September, the Stem Cell Research Team invited him back down to St Bart's to see if he was suitable for treatment under its new Compassionate Treatment Programme and treatment began in November.

Jenifer Rosenberg, chairwoman of the Heart Cells Foundation, said the programme's aim was to treat patients with severe heart disease with stem cell therapy on compassionate grounds to give them back their lives.

For five days, Gordon had injections to stimulate the growth of his own stem cells and on the sixth day, the team extracted bone marrow from the bottom of his back.

His bone marrow was sent by express courier across London to a laboratory where scientists extracted stem cells which were then put straight into the dead section of Gordon's heart muscle in an attempt to regenerate it. And it worked.

More news: Tributes as Bobby Kamara and Carlos Delgado die in Hull flat

"When I got back home, I felt really good," he said. "I could walk up the stairs without getting the pain and it was so marvellous."

Although he still has a lung condition and is about to begin another trial at Castle Hill Hospital in Cottingham to help his breathing, his heart continues to repair itself thanks to the stem cell treatment.

He said: "I will forever be thankful to the Heart Cells Foundation and the team at St Bart's. Without them, I wouldn't be here today and I'm enjoying every moment I spend with my wife and my children.

"Not only has the stem cell treatment I received helped to improve my physical health, but it has also massively improved my mental health and I now live every day with hope for the future."

Consultant cardiologist Professor Anthony Mathur, a director of interventional cardiology at St Bart's, said: "The launch of the programme is a momentous milestone in our research and Gordon's story proves just how important it is to offer cell therapy to those who have no other medical choice.

"With more than one million people suffering with heart disease and failure in the UK, the need for treatment in this field has never been greater.

"We hope to lead the way to the treatment ultimately being available to thousands of other patients through the NHS so we can help people like Gordon to lead near normal lives again."

Visit here to donate to Heart Cells Foundation and the Compassionate Treatment Programme.

More news: Travellers pitch up outside historic Lord Line in Hull

Excerpt from:
'Stem cells grew me a new heart' says Gordon Foster after treatment ... - Hull Daily Mail

Stem cell treatment effective in anterior cruciate ligament tear – Daijiworld.com

New Delhi, Feb 6 (IANS): With stem cell treatment effective in several health conditions, including spinal problems, doctors say the medical procedure can also help in speedy recovery of anterior cruciate ligament tear - a common chronic sports injury.

The medical procedure has advantage over surgeries because they are less invasive and focus on regeneration and healing of the tissues and ligaments rather than to cut and replace it.

In a case study, 28-year-old Mohan Verma - - a footballer suffering from anterior cruciate ligament was cured through Stem Cell treatment also known as Human Embryonic Stem Cell (HESC) in just eight months time.

Initially he was told to undergo a surgery and was informed that the complete recovery would take at least a year.

According to the doctors, HESC is used in three phases for ACL, so that the stem cells could grow, repair and regenerate the ligaments, tissues in the knee.

"Each treatment phase lasts 4-6 weeks during which 0.05 ml human embryonic stem cells is injected. The physician continuously administers the HESC. No immune-suppressants are given to the patients. In addition to HESC therapy, the patient receives physiotherapy and occupational therapy," said Geeta Shroff, stem cells specialist at Delhi-based Nutech Mediworld Hospital.

Comparing it to the conventional treatment, Shroff said: "In surgical procedure the graft goes in at a steeper angle than the original ACL which causes compression of the cartilage and hence most of the young athletes undergoing surgery end up with arthritis by the age of 30."

"Moreover the position sense and the strength of the knee can never be restored," she added.

Read this article:
Stem cell treatment effective in anterior cruciate ligament tear - Daijiworld.com

From Down syndrome to ‘near normal’? New Delhi clinic makes stem cell claims that worry experts – National Post


National Post
From Down syndrome to 'near normal'? New Delhi clinic makes stem cell claims that worry experts
National Post
A New Delhi clinic that has claimed to help paralyzed Canadians walk again by injecting them with stem cells now says it can use the same treatment to make children with Down syndrome almost near normal. Nutech Mediworld says it has treated up to 16 ...

Read more:
From Down syndrome to 'near normal'? New Delhi clinic makes stem cell claims that worry experts - National Post

Experimental Stem Cell Therapy Stops Multiple Sclerosis In Its … – Vocativ

The prognosis for people affected by multiple sclerosis (MS), a degenerative autoimmune disorder that decimates the central nervous system, is a bleak one. The disease oftenbegins with a sudden burst of neurological symptoms like muscle spasms, vision problems, and trouble walking, then progresses differently, depending on which form of MS someone has. But eventually, nearly everyone with the disease comesto the point of being unable to move, breathe, or live independently. And sufferers on average live anywhere from five to ten years less than the general public.

Currently, the best medications we have available do little more than slow MS down, or tamp down peoples symptoms. But an experimental therapy continues to provide the first glimmers of something ground-breaking an actual way to stop one form of the disease in its tracks, and maybe even reverse some of the damage already done.

In this months Neurology, researchers detailed the final five-year-old results of a small clinical trial called HALT-MS. Twenty-four volunteers with MS who hadnt responded to conventional drugs were first given a powerful form of chemotherapy, high-dose immunosuppressive therapy (HDIT), that wiped out their immune system. Then they were given a transplant of their own stem cells taken out earlier, known as autologous hematopoietic cell transplant (HCT). These purified cells, the researchers theorized, would seed a new generation of uncorrupted white blood cells and reset the immune system, freezing MS in its place.

For the most part thats exactly what the combination HDIT/HCT therapy did. Nearly 70 percent of patients, five years in, have experienced no signs of the disease progressing. They havent had a relapse of symptoms, become more disabled, or had new brain lesions show up in imaging exams. Some have actually improved physically in the years since the treatment. And even those not in complete remission appear to be suffering less than before. Importantly, though the treatment isnt free of side-effects, there havent been severe ones. There were three deaths seen during the trial, all of whom experienced worsening MS, but none were attributed to the treatment.

The volunteers all had relapsing-remitting MS, the most common form, in which symptoms come and go with little rhyme or reason.

The evidence at this time is encouraging, but it isnt definitive, study author Dr. Linda Griffith, a researcher at the National Institute of Allergy and Infectious Diseases (NIAID), which sponsored the study, told Vocativ.

As Vocativ has previously reported, this isnt the first trial to find similar success rates for HDIT/HCT, though it does come with its own dangers. Patients can die from it, and like all kinds of chemotherapy, the deliberate weakening of the immune system often leads to more infections. It also doesnt seem to be as effective for more advanced types of MS, when the disease has stopped causing active inflammation, said Griffith. And while it could be promising for people in the earliest stages of MS, the research needed to promote it as a first-line treatment isnt there yet either, she added.

For now, the only trials of HDIT/HCT have been small and isolated. And though the effects of it when successful seem to extend as far out as 13 years later, its too early to call it a full-on cure. We still dont have a clear grasp of why MS happens in the first place, but its thought that multiple triggers like infections and unlucky genetics combine to increase peoples risk. So even if resetting someones immune system does treat MS completely, its plausible that some percentage of patients could fall victim to it again down the road, Griffith explained. We just dont know enough right now.

But Griffith is hopeful that larger, randomized studies will be underway within the next year or so. And if those prove to be as successful as the HALT-MS trial and others, the therapy could someday soon lead to a light at the end of tunnel for the millions of MS sufferers alive today.

View original post here:
Experimental Stem Cell Therapy Stops Multiple Sclerosis In Its ... - Vocativ

Stem Cell Therapy Offers Hope to Multiple Sclerosis Patients (VIDEO) – Newsy

ByEthan Weston February 2, 2017

Stem cell research is making medical breakthroughs, and now, it could offer hope to people who have multiple sclerosis.

A newNational Institutes of Healthstudy suggests one-time stem cell transplants might be more effective than long-term medicinal treatment at treating relapsing-remitting MS.

Multiple sclerosis is an autoimmune disease that causes a person's immune system to attack their central nervous system. Common symptoms are impaired motor function, weakness and chronic pain. Relapsing-remitting MS is the most common form of the disease.

Stem cells are cells that haven't decided what they want to be when they grow up. That means they can develop into different types of cells. Because of that, they can be used to heal older damaged cells, like those attacked by the immune system.

The study followed 24 people who weren't having success with the typical MS medications. The experimental treatment suppressed participants' immune systems with chemotherapy. Then, their own stem cells were transplanted back into their bodies to rebuild their immune systems.

Related StoryPart-Pig, Part-Human Embryos Could Give Us Replacement Human Organs

Five years after treatment, most participants' symptoms were in remission. Some of them even showed some improvements.

Larger studies will be needed to confirm these findings. But the head of the study said it's a good first step toward more effective treatment for an incredibly debilitating and deadly disease.

See the original post:
Stem Cell Therapy Offers Hope to Multiple Sclerosis Patients (VIDEO) - Newsy

California’s stem cell program ponders a future of new challenges and old promises – Los Angeles Times

Evangelina Padilla Vaccaro of Coronais the new face of stem cell science in California. Born with bubble baby disease that deprived her of a functioning immune system, she was cured with stem cell therapy developed in Donald Kohns lab at UCLA, which has received millions of dollars in grants from the California stem cell program.

Now shes a vivacious 4-year-old, depictedastride a hobby horse and clad in a pink sweatshirt bearing a lightning bolton the programs 2016 annual report under the legend CURED.

Thank you all for the amazing work you do, her father told the program board during its Dec. 13 meeting.

Evangelina represents the great potential of the $3-billion state program, formally known as the California Institute for Regenerative Medicine, or CIRM, but also its dilemma as it ponders its next chapter. Established in 2004 by a nearly 60-40 vote for Proposition 71, CIRM began issuing grants in 2006. Now, after 10 years, the program has committed $2.2 billion of its bond-funded war chest. Its expecting to spend the rest by the end of 2020.

So it wont be long before CIRM must confront the question of whether to fold up shop when its well runs dry, seek outside funding from foundations and industry, or appeal to voters for more public money. If it returns to the ballot, CIRM would have a chance to reconsider its administrative structure, the inflated expectations it gave voters in 2004, its embedded conflicts of interestand even whether it should be limited to funding research into stem cells. All these features of Proposition 71 have created complications during the programsfirst decade.

Robert Klein II, the real estate investor who was the driving force behind Proposition 71 and chaired the institutefor its first seven years, already has said that he intends to place a funding measure on the November 2018 ballot.

CIRM officials, wary of rules limiting how far public agencies can go in lobbying for ballot measures, arent yettaking an official stand on Kleins effort. Were leaving it to Bob, Chairman Jonathan Thomas says; he told the oversight board in December, We keep him updated on CIRMs progress so that his effort is fully informed.

Thomas added, however, that he and other officers have started discussions with philanthropists and medical foundations that could be potential sources of funds to keep CIRM going in the event Bobs measure is not successful.Klein didnt respond to a requestfor comment.

The success of any ballot initiativewill depend on two factors, says Henry T. Greely, director of the Center for Law and the Biosciences at Stanford University: The two big variables are whether any of their clinical trials pay off, and what the Trump administration does.

The public wants evidence that its heavy investment in CIRM has yieldedcures for diabetes, Alzheimers, Parkinsons, spinal cord injuries orother conditions that were touted as research targets by the Proposition 71 campaign. Evangelinas improvement notwithstanding, no CIRM-funded research has yet reached the marketing stage, although CIRM officials say some initiativesare getting close.

Greelys allusion to White House policy harks back to the very genesis of the stem cell program, President George W. Bushs 2001 ban on federal funding for research on stem cellsderived from humanembryos. The imposition of an essentially ideological test forscientific research was what spurred California voters to enactProposition 71 as a constitutional amendment three years later. The measure endowed CIRM with $3 billion in bond revenue to fund California stem cell laboratories and attract world-class researchers.

The program certainly has helped turn California into a global center of stem cell research. California is the place to be if you want to develop stem cell treatments, says Jeanne Loring of Scripps Research Institute in La Jolla, a CIRM grantee who is researching possible treatments for Parkinsons.A lot of my colleagues in other states are envious.

President Obama lifted the Bush ban in 2009, but by then CIRMs role as a bulwarkof Californias research infrastructure was secure. Whether Trump might reimpose the ban is unknown.

Trump himself hasnt left a record of his views on embryonic stem cells, which typically are derived from unused embryos developed for in vitro fertilization and donated for research. ButVice President Mike Pence labeled suchresearch morally wrong in the pages of Christianity Today.

A new ballot campaign would present an opportunity to fix some of the stem cell programs flaws that were written into Proposition 71 and consequently embedded in the state Constitution.

The measure gave CIRM unique exemptions from most legislative oversight and state laws mandating public accountability and transparency. By dictating that seats on CIRMs 29-member oversight board would be filled almost exclusively by representatives of grant-eligible institutions or patient advocacy groups, it institutionalizedconflicts of interest and an atmosphere of cronyism.

The Institute of Medicine of the National Academy of Sciences found in a 2012 report that this setup bedeviled the program with persistent questions about the integrity and independence of some of CIRMs decisions. Indeed, an analysis by David Jensen of the California Stem Cell Report found that about 90% of the $1.7 billion in CIRM grants by 2013 had gone to institutions with present or past representatives on the board.

Lasting damage to CIRMs mission also may have been done by the tenor of the Proposition 71 campaign, which used such high-profile victims of neurological conditions as Michael J. Fox and Christopher Reeve to give voters the impression that money was the sole obstacle to miraculous stem cell cures, and that successful treatments would yield immense profits for the state. Neither claim was realistic, but they set benchmarks for success that CIRM has been unable to meet.

A new funding campaign could give the program a much-needed reboot. The ballot measure could restructure CIRM as an ordinary agency of the state subject to legislative oversight, open meetings lawsand other good-government statutes, says Marcy Darnovsky, executive director of the Berkeley-based Center for Genetics and Society.

Especially in its early years during Kleins chairmanship, the program guarded its independence from oversight truculently. Since then, Darnovsky says, its been more accommodating: Theyve been much better than they have to be by the letter of the law, she says approvingly. But she says the program has never resolved the conflicts of interest inherent in who decides where the money goes and who gets it.

A new campaign could instill more public realismabout the potential of the research being funded. If they ask for money, it would be really important that they level with the people of California and educate them about how science really works, Darnovsky said.

CIRMs leadership knows that the publics inflated expectations threaten to obscurethe programs real accomplishments. With multiple clinical trials of CIRM-funded researchunderway, the first government approval of treatments isexpected in the not-too-distant future, C. Randal Mills, the programs president, said in an interview.

But he acknowledged that expectations need to be tempered with humility at the enormity of the task before us. We dont want to overpromise or overhype. CIRM is doing what it was set up to do, but it might be taking longer than people thought or hoped.

Still, the programs future may depend more on politics than science. If it looks like Washington is flipping off California, that could have political ramifications at the ballot box, Greely says. Some researchers arent optimistic about the prospects for independent, federally funded science under the Trump administration.

The only thing Ican predict, Loring says, is that it will be neutral or negative. It wont be positive.

Keep up to date with Michael Hiltzik. Follow@hiltzikmon Twitter, see hisFacebook page, or emailmichael.hiltzik@latimes.com.

Return to Michael Hiltzik's blog.

Read more:
California's stem cell program ponders a future of new challenges and old promises - Los Angeles Times

Stem Cell Day of Discovery introduces students to USC scientists – USC News

You can be anything you want just like a stem cell. That was a key lesson for the 500 middle and high school students at the USC Stem Cell Day of Discovery on USCs Health Sciences Campus.

It was a true joy to welcome the middle and high school students from our neighboring communities in Boyle Heights, El Sereno, Lincoln Heights, the San Gabriel Valley and throughout Los Angeles, said Rohit Varma, dean of the Keck School of Medicine of USC. This bright young generation brings tremendous potential to their future pursuits in biotechnology and beyond.

Hosted by USC Civic Engagement and USC Stem Cell, the Feb. 4 event introduced the students to stem cell scientists.

Dont be shy, said Andy McMahon, director of the Eli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research at USC. Ask our scientists questions. Ask them about their science, but also ask them about their personal journeys that led to where they are.

The students followed McMahons advice as they engaged in fun activities and lively conversations. They visited labs to get hands-on experience with microscopes and pipettes. They competed as contestants in a stem cell edition of Family Feud, viewed colorful microscopy at a 3-D computer station and attended a research poster session and resource fair. They also toured the USC Norris Comprehensive Cancer Center and Keck Hospital of USC.

California currently has biotechnology as the biggest-growing sector, said junior Richard Coca of Reseda High School. Its really important that students are visiting labs and learning more about the industry so they can potentially see where theyre going with their lives and careers.

Stem cell technology

Earlier in the day, the students enjoyed hearing from Senta Georgia, a USC Stem Cell researcher with a lab at Childrens Hospital Los Angeles, who is seeking stem cell-based treatments for diabetes. Ismael Fernndez-Hernndez, a postdoctoral fellow at USCs stem cell research center from Guadalajara, Mexico, also gave a talk about how stem cell technology could offer ways to counteract brain degeneration from disease, aging or injury.

Throughout the festivities, Felipe Osorno, associate administrator of performance management for Keck Medicine of USC, served as master of ceremonies.

The exposure to the Keck School of Medicine of USC is invaluable for the students, said Maria Elena Kennedy, a consultant to the Bassett Unified School District. Our students come from a Title I School District and they dont often have the opportunity to come to a campus like the [one for the] Keck School.

In addition to students, teachers and parents, the event welcomed leaders from the community, business and biotech sector, and local government.

Together with these partners, USC will continue to build the future of Los Angeles as an incubator for the biosciences and world leader in stem cell research.

As USC continues the important work of expanding our biomedical research, we will not walk this path alone, said Earl C. Paysinger, vice president of USC Civic Engagement. We will do so in collaboration and with the strong support of the people in our communities.

More stories about: Community Outreach, Stem Cells

USC event in East L.A. on careers in STEM science, technology, engineering and math features retired astronaut and leading physician, both of them Trojans.

The annual open house offers art, research and networking opportunities.

In honor of Stem Cell Awareness Day, USC Stem Cell is hosting a series of public events to celebrate and raise awareness of this promising field of medicine.

Adnan Chowdhury ventures into uncharted scientific territory.

Visit link:
Stem Cell Day of Discovery introduces students to USC scientists - USC News