Could these senolytic drugs halt the spread of COVID-19? – Health Europa

Professor Michael P Lisanti, Chair in Translational Medicine at the University of Salford, has been an active research scientist for more than 30 years and is an expert in the field of cellular senescence. He tells HEQ about the potential of readily available, low cost, MHRA- and FDA-approved drugs to possibly treat and prevent the spread of COVID-19.

Senolytic drugs can be used to prevent or reverse ageing. There have been studies in mice that have shown that if you use a genetic trick, you can reverse ageing-associated disease characteristics but the problem is you cant do that in humans, so you would need a drug. We set out to identify drugs that would selectively kill senescent cells, but not harm normal cells; for this purpose, we developed a drug screen where we looked at various agents which prohibit cancer stem cell activity and we came across azithromycin, which selectively killed senescent cells with efficiency of nearly 97% and did not harm the normal cells. When we looked at the literature, we saw that patients with cystic fibrosis had been treated with azithromycin cystic fibrosis is similar to accelerated ageing as a disease, because theres a huge amount of inflammation and fibrosis and it dramatically increased their lifespan and their survival rates.

Fibrosis is normally an ageing-associated disease characteristic: its what kills patients with cystic fibrosis, because their lungs become stiff and can no longer expand and contract, in order to breathe. The azithromycin was also behaving as an antifibrotic, removing or preventing the formation of senescent myofibroblast cells; so we actually had proof In previous studies that our drug was actually a senolytic. If you reread the literature with senolytic glasses, you realise that the proof of its efficacy in humans is already there.

Another study in Japan looked at azithromycin based on its activity in cystic fibrosis patients and then applied these finding to patients with idiopathic pulmonary fibrosis. The control group survival rate in that paper was 25%, but on azithromycin it was nearly 80%. There is evidence in the published literature that its either preventing or removing fibrosis which is consistent with our data, but nobody thought about cystic fibrosis or about idiopathic pulmonary fibrosis as diseases of senescence: they thought it was preventing the formation of the myofibroblasts, but we believe it was killing the myofibroblasts, which are now known to be senescent cells.

The reason you want to get rid of the senescent cells is because they are actually contagious. They secrete IL-6, which is an inflammatory mediator; and they make other cells senescent by diffusion of the inflammatory mediators, which explains why as you get older you accumulate more and more senescent cells. By the time youre 40 or 50 years old, you have aches and pains and you feel stiffness: these are a symptom that you are beginning to accumulate senescent cells.

All of this is very reminiscent of what happens in patients with COVID-19. Fatality rates are much higher in older patients and in patients with ageing-associated diseases, such as diabetes or coronary artery disease. IL-6 levels have been shown to be the best predictor for whether or not a patient will to wind up on a respirator and these patients may die from inflammation in the lung and the resulting fibrosis. It all sounds similar to a very acute episode of either cystic fibrosis or of idiopathic pulmonary fibrosis.

The virus has something called a host receptor, which allows the virus to bind the surface of the cells and then get internalised. For COVID-19, there are two proposed host receptors: one is CD-26, which is a marker of senescence; and the other one is ACE-2, which is also increased during senescence. This would suggest that the virus is preferentially targeting cells with markers of senescence.

We think of senescent cells as old and not very energetic, but they have to secrete a lot of inflammatory mediators, like IL-6, so they actually have very active protein metabolism and they do a lot of protein synthesis IL-6 is a protein and they produce inflammatory mediators of the senescence associated secretory phenotype (SASP). Therefore, the virus would want to invade a cell that is better at protein synthesis in order to make more copies of itself and the necessary viral spiked glycoproteins, to package the viral RNA or DNA for viral replication. This virus is seeking out the cells that are the best at making protein, to make more copies of itself, so it gets in the cell and takes over.

The predilection for fatalities in patients with advanced chronological age suggests there is a connection with senescence; and azithromycin, which appears to be working in clinical trials, is a senolytic and an antifibrotic. Certain antibiotics of the azithromycin class of which there are many are inhibitors of protein synthesis. The same is true of tetracyclines like doxycycline. These drugs would inhibit protein synthesis, so they would block IL-6 production and also block viral replication. Azithromycin has been shown to inhibit Zika virus and Ebola virus replication; and doxycycline has been shown to inhibit Dengue virus replication. Any drug which is a protein synthesis inhibitor, like certain classes of antibiotics, would also inhibit viral replication not because of any characteristics specific to the virus, but because its inhibiting protein synthesis, which is required for their viral replication.

The question, then, is why we cant use these drugs now in the clinic. In the United States, if a drug is prescribed off-label, its perfectly legal: the FDA approves a drug after Phase 1, Phase 2 and Phase 3 clinical trials for a particular indication. Then because the drug already went through Phase 1, which is a safety trial, it can be legally prescribed for any other disease indication off-label. The FDA will not actually have to directly approve doxycycline or azithromycin for treatment of COVID-19, because doctors can already prescribe it.

In a time of crisis, we need to practise what people are calling battlefield medicine, where we think outside the box. Theres already evidence in the published literature that these antibiotics have the protein synthesis inhibition side effect and have already been shown to inhibit viral replication. The problem in this country is people are rightfully afraid of antibiotic resistance. Its the kind of thing that has been ingrained in the mindset of doctors in the UK. However, I think we need to rethink the whole use of antibiotics to target viral infections. In fact, if you look in the literature for herpes virus (HSV), its already been shown that erythromycin, which is another protein synthesis inhibitor, is used either orally or as a cream to treat herpes outbreaks.

If we could give NHS workers either doxycycline or azithromycin prophylactically, the viral load would likely be gone or severely diminished. This would prevent the spread of the virus from one person to another, protecting clinicians against people who come to the hospital; and could also be used to treat patients. But, I think the key here is to avoid the fibrosis and the inflammation, which starts with the fever. When a patient comes down with a fever, they should immediately give them the doxycycline or the azithromycin, which will shut down IL-6 production and shut down the viral replication; so the patient is less likely to transmit the disease to healthcare workers.

All these drugs are very inexpensive the cost of doxycycline is 10 pence a day; azithromycin is also very cheap, because it came off patent in 2017 so these drugs could be used for prophylaxis and for treatment. Then potentially we could relax some of the social distancing and we could all go back to work. The problem is were not going to have vaccines for another 12 to 24 months, so we need something now thats already safe, thats MHRA- or FDA-approved for at least one indication. It may be something that can be used in conjunction with social distancing: some people dont have extra space in their house where they can really isolate, so then they could take an antibiotic like doxycycline or azithromycin to reduce viral loads. This would reduce the stress on the healthcare system, because if you treat people in the early stages and it works, they wont get to the ventilator stage and the problem is when you get to the ventilator stage, the patients lungs have effectively turned to cement from all the fibrosis, so the chances of getting people off the ventilator is rather low. Its very serious once you get to the ICU, so you want to prevent the onset of respiratory symptoms, by treating patients as soon as possible with an antibiotic that will shut down viral replication.

Doxycycline is the number one drug prescribed worldwide for any indication: its used for malaria, its mainly used for acne; and people will take it for six months at a time without any real issues, except maybe some stomach upset. People with acne rosacea take it for their whole life, especially in very disfiguring cases usually they recommend a drug holiday for a week or two, every six months. Doxycycline was approved first in 1967. Its not a senolytic, but it does inhibit IL-6 and it inhibits viral replication; and it has been shown by other people to be an anti-ageing drug as well. Both of these drugs are very cheap; and they should be in abundant supply worldwide.

SARS-CoV-1, the precursor for COVID-19, shows the same pattern of infection. They conducted experiments in humans and mice and saw that, for example, young mice will become infected, but it doesnt cause any real disease there is no inflammation or fibrosis; and a very mild pneumonia but if they use older mice aged 12 to 14 months, they see very severe inflammation, fibrosis and death. This is due to the induction of a very strong inflammatory response, which includes the IL-6. This original mouse model could be used to test this hypothesis regarding senolytics, but as these drugs are already FDA-approved, we can do that in parallel. The problem is its a question of time; and the longer we wait, the more people are infected, when we could just shut it down now. We could use patients already in hospital, you would have instant clinical trials. This is battlefield medicine. We should take advantage of the patient population with drugs that have very few side effects, and conduct clinical trials on a large scale.

I think people are in a state of helplessness. They dont know what to do, and the solution could be right under our noses. What were doing is not working, for many patients, and we need to change something; and the first step would be propagate the idea of field clinical trials. We can record all the data from the treatment of the patients as it progresses thousands of people have the disease and it could be a multicentre trial, the most important thing is to get something going now.

Much research into the treatment of COVID-19 is currently focused on the drugs chloroquine and azithromycin; and the FDA has granted an emergency licence for the use of chloroquine to treat COVID-19 patients. The European Medicines Agency has not yet followed suit, asserting that more research should be conducted; and some researchers have highlighted concerns over toxicity issues associated with chloroquine and its derivative, hydroxychloroquine.

Patients who are prescribed chloroquine or hydroxychloroquine normally would have to take a test for a glucose-6-phosphate dehydrogenase deficiency (G6PD) [an hereditary condition which increases the risk of haemolysis when chloroquine is administered]; and there are other issues with both chloroquine and hydroxychloroquine. I think the side effects may outweigh the benefits, because its not an inhibitor of viral replication; its an inhibitor of viral entry. If the patient is already sick, they already had the viral entry, then chloroquine will not necessarily shut down the viral replication. It only works for patients who have not already been infected.

In the clinical data from the French trial of hydroxychloroquine and azithromycin, the chloroquine did relatively little by itself and that has been called into question in terms of the effects. The combination with azithromycin was much more effective, but they didnt test azithromycin alone, which would probably be sufficient; because even if viral entry does occur, as long as the viral replication is inhibited, the virus will not propagate. We believe that the hydroxychloroquine isnt necessary; and we can reduce the risk to older patients by eliminating the hydroxychloroquine.

Azithromycin has some very mild side effects, but theyre not very prevalent; if they had been prevalent the drug would have been pulled off the market. There was some controversy as to the reproducibility of the studies regarding its side effects: multiple studies were done and some are positive, some are negative, so theres still a warning out there but the side effects only really occur with high doses of azithromycin, which would not be needed in this case. If azithromycin did cause problems for a patient they could switch to doxycycline, or they could start with doxycycline in the first place. These are just two examples of classes of drugs; there are other drugs which inhibit protein synthesis: erythromycin is in the same class as azithromycin, and it inhibits protein synthesis. It doesnt have the senolytic activity, but it would still inhibit the IL-6 and the viral replication.

The same is the case for the tetracyclines these are classes of drugs which are relatively similar and interchangeable, so if we run out of doxycycline, we would still have minocycline, tetracycline and all these other variations which have a similar effect on protein synthesis. The main issue with doxycycline is patients can experience some stomach upset or some nausea, but this can be alleviated by using a probiotic.

That would be the primary role of these drugs. Based on the results of clinical trials, the NHS could implement its usage. For example, ICU staff could receive it first, as they are in contact with patients that pose the most severe risk. Hospital staff right now are probably terrified of catching it, so why not take a prophylactic antibiotic, which has a chance of preventing infection? Im sure theyre doing a great job taking care of the patients, but it is traumatic to be under all this stress constantly. Its very stressful to be in such a high pressure situation, where youre afraid for your own life, but youre also trying to help other people at the same time. Then, you have your family at home and you dont want to also make them sick either. Healthcare workers are the people who are at the greatest risk; and already weve seen a reduction in NHS staff levels around one in four NHS staff are not at work, because they have either been infected or are isolating because they have symptoms.

We dont want to lose too many of the doctors and nurses in this crisis, so this would be helpful for everyone especially for preventing the further spread to shut down viral replication and contagion. Anything that can be done to reduce the viral load will reduce the contagion. They can do trials with young healthy volunteers who are asymptomatic, but it would be better to do it with the NHS staff who would need it most as a preventative approach for prophylaxis. We have recently proposed and published this prophylaxis strategy in a Letter to the Editor at the British Medical Journal (BMJ), which is widely read by GPs and consultants in the UK.

1 Letter to the Editor, British Medical Journal: https://www.bmj.com/content/368/bmj.m1252/rr-20

2 Lisanti, Sotgia et al. (2020). Senescence, ageing and potential COVID-19 treatments. Aging-US. https://www.aging-us.com/article/103001/text

Professor Michael P Lisanti, MD-PhD, FRSA, FRSBChair in Translational MedicineSchool of Science, Engineering & EnvironmentUniversity of Salford+44 (0)1612 950 240M.P.Lisanti@salford.ac.uk

This article is from issue 13 of Health Europa. Clickhere to get your free subscription today.

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Could these senolytic drugs halt the spread of COVID-19? - Health Europa

Doctors revealed details of the new rescue of Michael Schumacher – The Times Hub

Legendary German racing driver expects to implement the next batch of stem cells into heart tissue

Sevenfold champion of Formula 1 Michael Schumacher will have to go through another operation, according to GrandPX with reference to the Italian source Contro Copertina. As noted cardiac surgeon, Dr. Phillip Menashe, who was already engaged in treatment of the legendary German racer earlier, Schumacher will conduct the experimental operation on the introduction of stem cells into heart tissue.

Last year it was reported that Michael has already passed a similar procedure. The goal is to restore the nervous system Michael, said Menashe.

Neurosurgeon Dr. Nikola Acciari told that a famous former pilot Ferrari also suffers from muscle atrophy and osteoporosis. Over the last 20 years science has made enormous progress in the field of stem cell treatment. But it doesnt change the fact that we still know little about the human brain. We cant tell what results it will bring, said the doctor.

Michael Schumacher. Photo skysports.com

Recall Michael Schumacher suffered a severe head injury in December 2013 in the result of a fall at a ski resort in France. Since then Schumacher, who in January turned 51, never appeared in public.

About the state of his health there is no reliable information because the family prefers to keep it a secret. However, last fall it became known that Michael Schumacher is secretly transported to a clinic in Paris. In this case an unnamed member of the medical personnel told reporters: He is conscious.

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Doctors revealed details of the new rescue of Michael Schumacher - The Times Hub

Autologous Bone Marrow Transplantation and Metformin, a Hope for the Cure of Multiple Sclerosis – Gilmore Health News

On Friday, June 5, a few days after World MS Day on May 30, there was a day of online conferences and workshops to learn more about multiple sclerosis. It was an opportunity to shed light on autologous bone marrow transplantation, a little known treatment that could cure multiple sclerosis.

Neuron

Multiple sclerosis (MS) is a neurodegenerative autoimmune disease that causes stiffness, pain, and fatigue. It is the main cause of disability, exclusion from the labor market, and social exclusion among young people, as it occurs mainly among people between 25 and 35 years old. According to the National MS Society, approximately 1 million people in the United States suffer from MS.

Currently, there is no treatment to cure MS, but there is hope: Autologous bone marrow transplantation or autologous hematopoietic stem cell transplantation. This treatment allows patients to go from the more common forms of multiple sclerosis into remission. If carried out early enough, it enables at least partial recovery from the disability.

Read Also: Combo of Diabetes and Hypertension Drugs Causes Cancer Cell Death, Researchers Find

The aim of this treatment is to rebuild a new immune system in patients. This includes intensive chemotherapy followed by reinjection of the patients hematopoietic stem cells. Several studies conducted between 2015 and 2019 on this technique have shown that 83.3 of patients with the relapsing-remitting form had no attack in the four years following auto-transplantation and three years after transplantation 78% of patients with secondary progressive multiple sclerosis and 66% of patients with primary progressive multiple sclerosis experienced no worsening of their disability, Mediapart continues.

One of the main obstacles to this treatment remains the difficulty of access. Many patients testify that their neurologist often finds this method too experimental and too risky. Another factor that discourages the use of autologous bone marrow transplantation is the risk-benefit ratio, which is considered unbalanced. Transplant-related mortality is between 5 and 10%, which justifies doctors preference for a treatment that is considered safer.

Read Also: Diabetes: Metformin Transfers Blood Sugar From the Blood to the Intestines

Another treatment has shown encouraging results in multiple sclerosis. This is a drug for diabetes, metformin, which rejuvenates stem cells to convert them into myelin-producing cells and thus help combat multiple sclerosis. These results have been published in the journal Cell Stem Cell, and it is expected that the tests, which are currently only carried out on mice, will also be carried out on humans within a year. I am very optimistic, study author Professor Robin Franklin told The Guardian newspaper.

References

Metformin Restores CNS Remyelination Capacity by Rejuvenating Aged Stem Cells

https://blogs.mediapart.fr/noelle-tassy/blog/300520/journee-mondiale-de-la-sep-et-si-parlait-du-traitement-dont-ne-parle-pas

Autologous Hematopoietic Cell Transplantation in Multiple Sclerosis: Changing Paradigms in the Era of Novel Agents

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Autologous Bone Marrow Transplantation and Metformin, a Hope for the Cure of Multiple Sclerosis - Gilmore Health News

R3 International Now Offering New Stem Cell Therapy Program for Lyme Disease in Mexico – Yahoo Finance

R3 Stem Cell International announced that it is now offering a new program with stem cell therapy for Lyme disease. R3 has been offering effective treatment at its international clinics for a while, but with the new program patients receive more cost effective options with 100 to 200 million stem cells involved.

SAN DIEGO, June 8, 2020 /PRNewswire-PRWeb/ -- R3 Stem Cell International announced that it is now offering a new program with stem cell therapy for Lyme disease. R3 has been offering effective treatment at its international clinics for a while, but with the new program patients receive more cost effective options with 100 to 200 million stem cells involved.

Stem cell treatment for Lyme disease in Mexico has been very effective at helping patients achieve symptom relief and regain an improved quality of life. Depending on a patient's history, the R3 International licensed provider will decide whether to add additional exosomes along with stem cells to the regimen.

The new program for Lyme disease involves either 150 million stem cells or 200 million. While these cell counts are incredibly high, it needs to be noted that the biologics come from a Mexico lab that achieves quality standards that exceed those of the FDA in the US.

There are two options for the Stem Cell Lyme disease program. One is a 5 day stay where Lyme patients receive several treatments during that time. The second option is for a patient to return to the Center for four visits over a year. The decision of which program to participate in is up to the patient and his/her family.

R3 Stem Cell International in Tijuana Mexico is only 20 minutes from the San Diego International Airport. R3 provides concierge escorted transportation to and from the clinic from San Diego, with hundreds of patients over the past year receiving successful care at the modern center.

The stem cell and exosome biologics used for Lyme disease care come from a lab that has an incredible safety record, and each treatment's biologic comes with a full Certificate of Analysis. Because Mexico allows stem cell culturing, the cell counts are extremely high with a viability of over 90%. No preservative is even necessary.

According to R3 International CEO David Greene, MD, MBA, "Patients and their families dealing with Lyme disease deserve a safe, clinically effective and cost effective option. We put that together in Mexico, with all inclusive treatment starting at $8975 which includes hotel and ground transportation. Tough conditions like Lyme disease necessitate large cell counts for optimal outcome, and most international centers charge 3 to 5 times our fees. Not with us!"

Each patient undergoes a free phone consultation with R3 International's licensed, experienced stem cell doctor. Simply call (888) 988-0515 to set one up.

SOURCE R3 Stem Cell International

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R3 International Now Offering New Stem Cell Therapy Program for Lyme Disease in Mexico - Yahoo Finance

Nick Cordero’s Wife Says His COVID-19 Recovery Is ‘Going in the Right Direction’ – countryliving.com

Nick Cordero's wife, Amanda Kloots, shared a hopeful update on her husband's condition as he continues to recover from his battle with COVID-19 and related complications.

In a series of videos posted to her Instagram stories on Sunday, Amanda said, "S0 I think this weekend was a good weekend, it was uneventful. Which, uneventful in the ICU is a good weekend. I think he had a weekend of rest, a weekend of growing, strength in his body and recovering a little bit."

"Not too many changes were made, which is also a good sign, but one really good sign is his white blood count number is way down," she continued. "So it has been as high as 65,000; we are now at 30,000. A frame of reference: a normal healthy person is around 15-20,000, even lower sometimes. So 30,000 is a great sign that things are moving in the right direction."

The Tony Award-nominated Broadway actor has been hospitalized at Cedars-Sinai Medical Center in Los Angeles for more than two months after being diagnosed with COVID-19.

Amanda's optimistic update comes almost a month after her husband woke up from a medically-induced coma and almost two months after he had his right leg amputated due to blood-clotting complications from the virus.

Nick, who is also known for his recurring roles on Blue Bloods and Law & Order: SVU, has started stem cell treatment to help his recovery, Amanda shared in another recent Instagram story.

"This could be really great ... Even if it just bridges us to the next level in healing for him," she said on Friday.

Amanda ended her weekend Instagram stories on a positive note, saying, "I don't know why I just have a really good feeling about this week, so I'm just gonna keep praying for our miracles and keep praying for that healing and God is with us ... Love you!"

We are also praying for Nick's full recovery and wishing him and his family all the best during this difficult time.

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Memorial Sloan Kettering – Hackensack Meridian Health Partnership Announces Funding for Inaugural Immunology Research Collaboration Projects – The…

HACKENSACK, N.J. and NEW YORK, June 5, 2020 /PRNewswire/ -- As part of the Memorial Sloan Kettering Hackensack Meridian Health Partnership, the two organizations have formed an Immunology Research Collaboration. Through this joint initiative, researchers can apply for funding to support innovative investigations to explore the power of the immune system and ways it may be harnessed to fight cancer.

The three researchers with projects selected in 2020 for funding support over one to two years are:

"Immunotherapy has become an essential pillar of cancer treatment, but much remains to be discovered about the immune system and new ways to take advantage of its power to treat cancer effectively," said Paul Sabbatini, M.D., deputy physician-in-chief for clinical research at Memorial Sloan Kettering. "The Immunology Research Collaboration between Memorial Sloan Kettering and Hackensack Meridian Health gives researchers an opportunity to delve deeply into unexplored facets of the immune system, both in the lab and clinic, and speed discoveries that will ultimately contribute to reducing the burden of cancer on our patients, their families, and the world. We are enthusiastic about the potential of these three research projects and look forward to their results."

"While immunotherapy is revolutionizing cancer treatment, its benefits are not always sustainable over the long term," noted Andrew Goy, M.D., M.S., chairman and executive director of John Theurer Cancer Center and physician-in-chief of the Hackensack Meridian Health Oncology Care Transformation Service. "The work of these investigators will expand our knowledge of the immune system and glean new insights which may lead to novel immunotherapeutics that are more powerful and more durable than those we are using today. These projects capture the collaborative spirit of this initiative and could have a significant impact on patient outcomes."

ABOUTHACKENSACKMERIDIAN HEALTH

Hackensack Meridian Health is a leading not-for-profit health care organization that is the largest, most comprehensive and truly integrated health care network in New Jersey, offering a complete range of medical services, innovative research and life-enhancing care.

Hackensack Meridian Health comprises 17 hospitals from Bergen to Ocean counties, which includes three academic medical centers Hackensack University Medical Center in Hackensack, Jersey Shore University Medical Center in Neptune, JFK Medical Center in Edison; two children's hospitals - Joseph M. Sanzari Children's Hospital in Hackensack, K. Hovnanian Children's Hospital in Neptune; nine community hospitals Bayshore Medical Center in Holmdel, Mountainside Medical Center in Montclair, Ocean Medical Center in Brick, Palisades Medical Center in North Bergen, Pascack Valley Medical Center in Westwood, Raritan Bay Medical Center in Old Bridge, Raritan Bay Medical Center in Perth Amboy, Riverview Medical Center in Red Bank, and Southern Ocean Medical Center in Manahawkin; a behavioral health hospital Carrier Clinic in Belle Mead; and two rehabilitation hospitals - JFK Johnson Rehabilitation Institute in Edison and Shore Rehabilitation Institute in Brick.

Additionally, the network has more than 500 patient care locations throughout the state which include ambulatory care centers, surgery centers, home health services, long-term care and assisted living communities, ambulance services, lifesaving air medical transportation, fitness and wellness centers, rehabilitation centers, urgent care centers and physician practice locations. Hackensack Meridian Health has more than 35,000 team members, and 7,000 physicians and is a distinguished leader in health care philanthropy, committed to the health and well-being of the communities it serves.

The network's notable distinctions include having four hospitals among the top in New Jersey by U.S. News and World Report. Other honors include consistently achieving Magnet recognition for nursing excellence from the American Nurses Credentialing Center and being named to Becker's Healthcare's "150 Top Places to Work in Healthcare/2019" list.

The Hackensack Meridian School of Medicine at Seton Hall University opened in 2018, the first private medical school in New Jersey in more than 50 years, welcomed its second class of 96 students in 2019 to its ON3 campus in Nutley and Clifton. Additionally, the network partnered with Memorial Sloan Kettering Cancer Center to find more cures for cancer faster while ensuring that patients have access to the highest quality, most individualized cancer care when and where they need it.

Hackensack Meridian Health is a member of AllSpire Health Partners, an interstate consortium of leading health systems, to focus on the sharing of best practices in clinical care and achieving efficiencies.

For additional information, please visit http://www.HackensackMeridianHealth.org.

ABOUT MEMORIAL SLOAN KETTERING

As the world's oldest and largest private cancer center, Memorial Sloan Kettering has devoted more than 135 years to exceptional patient care, influential educational programs, and innovative research to discover more effective strategies to prevent, control and, ultimately, cure cancer. MSK is home to more than 20,000 physicians, scientists, nurses, and staff united by a relentless dedication to conquering cancer. Today, we are one of 51 National Cancer Institute-designated Comprehensive Cancer Centers, with state-of-the-art science and technology supporting groundbreaking clinical studies, personalized treatment, and compassionate care for our patients. We also train the next generation of clinical and scientific leaders in oncology through our continually evolving educational programs, here and around the world. Year after year, we are ranked among the top two cancer hospitals in the country, consistently recognized for our expertise in adult and pediatric oncology specialties. http://www.mskcc.org.

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Memorial Sloan Kettering - Hackensack Meridian Health Partnership Announces Funding for Inaugural Immunology Research Collaboration Projects - The...

Reports: F1 Legend Michael Schumacher is Set for Another Operation on His Road to Recovery – Essentially Sports

F1 and Ferrari legend Michael Schumacher is all set for another operation as he continues on his road to recovery. It has been 6 and a half years since Schumacher suffered a brain injury when he had a skiing accident in the French Alps. After the first couple of years, news has been scarce regarding the health of the 7-time world champion. However, in a bit of an update, Schumi is scheduled for a transfusion.

Italian source, Contro Copertina claims the aforementioned. They say that Dr Philippe Menasche, who is regarded as a pioneer in cell surgery will be in charge of the operation. Menasche was also in charge of a similar operation on Schumacher last year. Regarding the aim of the operation, Menasche said, The goal is to regenerate Michaels nervous system.

Dr Nicola Acciari claims that Michael Schumacher is suffering from muscle atrophy and osteoporosis. Both these conditions arise due to the lack of physical activity. Acciari adds, Over the past 20 years, science has made enormous progress in the field of stem cell treatment. But that doesnt change the fact that we still know little about the human brain. We are not able to say what results it (the treatment) will bring.

Earlier this year, When Dr Nicola Acciari spoke to Contro Copertina she had said, We must imagine a person very different from the one we remember on the track, with a very altered and deteriorated organic, muscular and skeletal structure. All as a result of the brain trauma he suffered.

Generally, the Schumachers have been very private about any news about the F1 legends health. However, Former Ferrari team principal, Jean Todt had revealed last year, that he had watched a race with Schumi at the Germans house in Switzerland. Todt said, He does not give up and keeps fighting.

We wish Schumi the best of luck on his road to recovery.

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KOCO 5’s Zach Rael heading to California to help cousin with rare form of blood cancer – KOCO Oklahoma City

KOCO 5 reporter and anchor Zach Rael is heading to California to help his cousin in a battle against a rare form of blood cancer called myelofibrosis.Raels cousin reached out to him about eight months ago for him for help, saying her brother had been diagnosed with myelofibrosis. Rael said his cousin is doing well and there is an up-and-coming treatment that requires a healthy person to donate their stem cells from their blood.Ideally, the donor is a family member because there is a high chance of a match and a positive result, Rael posted on social media.Tests revealed that many family members were not suitable donors, so the family reached out to Rael and others with the hopes that someone would be a match. Rael submitted his DNA and, a few weeks later, learned he was a match.Rael took a flight Tuesday to California, where he will be for the next 10 days as part of the donation process.Over the next few days, I will be documenting my experience, he wrote. I plan on posting daily updates on my social media accounts and will be putting together a special story for air on KOCO when Im done.You can read Raels full story below:Hello everyone! I hope you are doing well on this Tuesday. Im writing this while on board an airplane somewhere over Arizona, on my way to Los Angeles, California. This is my first time flying post-pandemic. Besides the face masks - its been relatively normal.Unfortunately, this is not a vacation or a trip for fun.About 8 months ago my cousin Kathy (2nd cousin on my moms side) reached out to me asking for help. Her brother, my cousin Don, is battling Myelofibrosis, a rare form of blood cancer. While any type of cancer is scary, he is doing as well as he can and luckily there is an up and coming treatment used to treat it. The treatment essentially requires a healthy person to donate their stem cells from their blood to the person with cancer (Ill explain more on that later). Ideally, the donor is a family member because there is a high chance of a match and a positive result.Don and Kathy had already asked all their extended family to submit their DNA, but to no luck. No one came back as a suitable donor. So, they opened the search to extended family and I happily agreed to submit my DNA. Basically, I got a tube in the mail and was asked to spit in it. A few weeks later and I got a call from my cousins that I came back as a match to submit my stem cells to my cousin Don!Truth be told, before all of this, I was not very close with this side of my family. As it happens with extended family - we would only see each other at special family events like weddings, graduations, or funerals. So, I was a little surprised that I came back as a match. But I could not be more thrilled I did! This will be the best possible shot of giving cousin Don a chance to beat this thing!Flash forward to today. Ill be in California for the next 10 days as part of the donation process.A quick breakdown of what is to come: once I land, I will be going straight to City of Hope, the hospital system that is performing the donation and treating Don. They will be running some final tests on me this afternoon, including taking 20 of my vitals (Im told this is normal). Later this week I will have to take a COVID-19 test, an information class, and receive a few dosages of special shots. Ill be taking these shots once a day for 5 days before the donation. They help generate my stem cells so they are more easily extracted. One week from today will be my actual donation. It is a 6-8 hour process where I will be hooked up to a machine. They will take my blood from one arm, run it through a machine, and put my blood back in me through my other arm. Im told its just like giving blood.Over the next few days I will be documenting my experience (see the pic with all my equipment). I plan on posting daily updates on my social media accounts and will be putting together a special story for air on KOCO when Im done. My bosses at KOCO have been so understanding and willing to do what they can so I was able to come out to California for nearly two weeks. Im so thankful.Anyway this post is getting long. I hope you follow along and I hope to shed some light on what it is like to become a stem cell donor. There is a HUGE need for them.Talk soon. Cheers!-Zach

KOCO 5 reporter and anchor Zach Rael is heading to California to help his cousin in a battle against a rare form of blood cancer called myelofibrosis.

Raels cousin reached out to him about eight months ago for him for help, saying her brother had been diagnosed with myelofibrosis. Rael said his cousin is doing well and there is an up-and-coming treatment that requires a healthy person to donate their stem cells from their blood.

Ideally, the donor is a family member because there is a high chance of a match and a positive result, Rael posted on social media.

Tests revealed that many family members were not suitable donors, so the family reached out to Rael and others with the hopes that someone would be a match. Rael submitted his DNA and, a few weeks later, learned he was a match.

Rael took a flight Tuesday to California, where he will be for the next 10 days as part of the donation process.

Over the next few days, I will be documenting my experience, he wrote. I plan on posting daily updates on my social media accounts and will be putting together a special story for air on KOCO when Im done.

You can read Raels full story below:

Hello everyone! I hope you are doing well on this Tuesday. Im writing this while on board an airplane somewhere over Arizona, on my way to Los Angeles, California. This is my first time flying post-pandemic. Besides the face masks - its been relatively normal.

Unfortunately, this is not a vacation or a trip for fun.

About 8 months ago my cousin Kathy (2nd cousin on my moms side) reached out to me asking for help. Her brother, my cousin Don, is battling Myelofibrosis, a rare form of blood cancer. While any type of cancer is scary, he is doing as well as he can and luckily there is an up and coming treatment used to treat it. The treatment essentially requires a healthy person to donate their stem cells from their blood to the person with cancer (Ill explain more on that later). Ideally, the donor is a family member because there is a high chance of a match and a positive result.

Don and Kathy had already asked all their extended family to submit their DNA, but to no luck. No one came back as a suitable donor. So, they opened the search to extended family and I happily agreed to submit my DNA. Basically, I got a tube in the mail and was asked to spit in it. A few weeks later and I got a call from my cousins that I came back as a match to submit my stem cells to my cousin Don!

Truth be told, before all of this, I was not very close with this side of my family. As it happens with extended family - we would only see each other at special family events like weddings, graduations, or funerals. So, I was a little surprised that I came back as a match. But I could not be more thrilled I did! This will be the best possible shot of giving cousin Don a chance to beat this thing!

Flash forward to today. Ill be in California for the next 10 days as part of the donation process.

A quick breakdown of what is to come: once I land, I will be going straight to City of Hope, the hospital system that is performing the donation and treating Don. They will be running some final tests on me this afternoon, including taking 20 of my vitals (Im told this is normal). Later this week I will have to take a COVID-19 test, an information class, and receive a few dosages of special shots. Ill be taking these shots once a day for 5 days before the donation. They help generate my stem cells so they are more easily extracted. One week from today will be my actual donation. It is a 6-8 hour process where I will be hooked up to a machine. They will take my blood from one arm, run it through a machine, and put my blood back in me through my other arm. Im told its just like giving blood.

Over the next few days I will be documenting my experience (see the pic with all my equipment). I plan on posting daily updates on my social media accounts and will be putting together a special story for air on KOCO when Im done. My bosses at KOCO have been so understanding and willing to do what they can so I was able to come out to California for nearly two weeks. Im so thankful.

Anyway this post is getting long. I hope you follow along and I hope to shed some light on what it is like to become a stem cell donor. There is a HUGE need for them.

Talk soon. Cheers!

-Zach

Read the rest here:
KOCO 5's Zach Rael heading to California to help cousin with rare form of blood cancer - KOCO Oklahoma City

COVID-19 Impact on Global Cancer Stem Cell Therapy Industry 2020: Market Trends, Size, Share, Growth Applications, SWOT Analysis by Top Key Players…

The Global Cancer Stem Cell Therapy Market was estimated to be valued at USD XX million in 2019 and is projected to reach USD XX million by 2026, at a CAGR of XX% during 2019 to 2026.

The market is primarily driven by increasing number of cancer patients suffering from many different types of cancer. In addition, stem cell therapy is a painless and incision less treatment procedure is likely to boost the market growth.

However, lack of suitable and donor matching sample might restrict the market growth.

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Development policies and plans are discussed as well as manufacturing processes and cost structures are also analyzed. This report also states import/export consumption, supply and demand Figures, cost, price, revenue and gross margins.

Top Key Companies Analyzed inGlobal Cancer Stem Cell Therapy Market are Thermo Fisher Scientific, Merck Kgaa, Bionomics, Lonza, Stemline Therapeutics, Miltenyi Biotec, Promocell, Macrogenics, Oncomed Pharmaceuticals and Irvine Scientific

Key Benefit of This Report:

Global Cancer Stem Cell Therapy Industry 2019 Market Research Report is spread across 121 pages and provides exclusive vital statistics, data, information, trends and competitive landscape details in this niche sector.

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Target Audience:

Research Methodology:

The market is derived through extensive use of secondary, primary, in-house research followed by expert validation and third party perspective, such as, analyst reports of investment banks. The secondary research is the primary base of our study wherein we conducted extensive data mining, referring to verified data sources, such as, white papers, government and regulatory published articles, technical journals, trade magazines, and paid data sources.

For forecasting, regional demand & supply factors, recent investments, market dynamics including technical growth scenario, consumer behavior, and end use trends and dynamics, and production capacity were taken into consideration.

Different weightages have been assigned to these parameters and quantified their market impacts using the weighted average analysis to derive the market growth rate.

The market estimates and forecasts have been verified through exhaustive primary research with the Key Industry Participants (KIPs), which typically include:

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Major Points Covered in Table of Contents:

1 Introduction

2 Research Methodology

3 Executive Summary

4 Global Cancer Stem Cell Therapy Market Overview

5 Global Cancer Stem Cell Therapy Market, by Product Type

6 Global Cancer Stem Cell Therapy Market, by Application

7 Global Cancer Stem Cell Therapy Market by Region

8 Competitive Landscape

9 Company Profiles

10 Key Insights

Customization Service of the Report:Orian Research provides customisation of reports as per your need. This report can be personalised to meet your requirements. Get in touch with our sales team, who will guarantee you to get a report that suits your necessities.

About Us:Orian Research is one of the most comprehensive collections of market intelligence reports on the World Wide Web. Our reports repository boasts of over 500000+ industry and country research reports from over 100 top publishers. We continuously update our repository so as to provide our clients easy access to the worlds most complete and current database of expert insights on global industries, companies, and products. We also specialize in custom research in situations where our syndicate research offerings do not meet the specific requirements of our esteemed clients.

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COVID-19 Impact on Global Cancer Stem Cell Therapy Industry 2020: Market Trends, Size, Share, Growth Applications, SWOT Analysis by Top Key Players...

Saudi Govt. Stresses Need to Respect COVID-19 Preventive Measures – Asharq Al-awsat – English

The Saudi government stressed on Tuesday the need for citizens and residents to adhere to the preventive measures aimed at curbing the novel coronavirus.

Custodian of the Two Holy Mosques King Salman bin Abdulaziz chaired the virtual cabinet meeting.

The ministers reviewed the measures the Kingdom has been taking to ease the restrictions imposed over the outbreak.

King Salman emphasized that the health of the citizens and residents was his top priority.

The cabinet hailed the huge support King Salman and Crown Prince Mohammed bin Salman, Deputy Prime Minister and Minister of Defense, have offered the concerned sectors, allowing them to improve their efforts in preparing for and containing the outbreak.

They praised the concerned authorities for raising awareness among the people, maintaining the health sector and doubling the capacities of labs, intensive care units and number of ventilators.

The cabinet expressed its great confidence in the capacity of the health sector and its advanced capabilities, which were provided by the wise leadership through financial and moral support.

It noted the states investment in the health infrastructure over the years, which has allowed it to respond rapidly and with high efficiency to the challenges caused by the pandemic. This has enabled it to provide health care to all despite the difficult conditions sparked by the outbreak and effectively saving lives.

The government also addressed last week's 2020 donor conference for Yemen that was hosted by Saudi Arabia in partnership with the United States at the directives of King Salman and Crown Prince Mohammed. The event saw the participation of 126 parties from 66 countries, as well as several UN and non-government agencies. The conference pledged 1.35 billion dollars for Yemen, including 50 million pledged by Saudi Arabia.

The Kingdom will continue to support the Yemeni people and exert all efforts to reach a sustainable political solution to their conflict.

The cabinet reviewed the latest regional and international developments. It again welcomed Egypts efforts that are aimed at resolving the Libyan conflict. The Cairo Declaration, announced on Saturday, called for a ceasefire, resuming political talks and electing a leadership council.

The ministers also rejected Israels plans to annex territories in the occupied West Bank, condemning any potential unilateral measures and any violations of international resolutions. The ministers also expressed their rejection of any move that would hamper the resumption of the peace process that is aimed at achieving security and stability in the region. Saudi Arabia remains committed to Palestinian people and their choices.

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Saudi Govt. Stresses Need to Respect COVID-19 Preventive Measures - Asharq Al-awsat - English