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Cleveland Clinic Appoints Timothy Chan, M.D., Ph.D., as Director of Center for Immunotherapy and Precision Immuno-Oncology – Health Essentials from…

Posted: April 27, 2020 at 2:49 pm

Timothy Chan, M.D., Ph.D.

Timothy Chan, M.D., Ph.D., has been appointed director of the Center for Immunotherapy and Precision Immuno-Oncology at Cleveland Clinic.

A renowned immuno-oncology and cancer genomics expert, Dr. Chan leads the new center which brings together multidisciplinary experts from across the Cleveland Clinic enterprise to advance research and treatment related to the rapidly growing field of immuno-oncology.

The center will comprise four arms, including a Cleveland cell therapy program in collaboration with the Case Comprehensive Cancer Center, and will recruit national and international experts in computational science, immunotherapy and cancer immunology. The new center will initially have sites in Cleveland and the soon-to-open Cleveland Clinic Florida Research and Innovation Center in Port St. Lucie, Florida, both focused on immunotherapy research and developmental therapeutics.

Dr. Chan will also collaborate with experts in the new Center for Global and Emerging Pathogens Research, which is focused on broadening understanding of immunology and microbial pathogenesis with the goal of improving treatment for a variety of diseases, including virus-induced cancers.

Immunotherapy is the future of research in cancer and various other diseases and Cleveland Clinic has made it a priority by establishing this new center, said Serpil Erzurum, M.D., chair of Cleveland Clinics Lerner Research Institute. The Center for Immunotherapy and Precision Immuno-Oncology will empower clinicians and scientists throughout the enterprise to advance personalized cancer care and breakthrough immunotherapy research at Cleveland Clinic.

Dr. Chan joins Cleveland Clinic from Memorial Sloan Kettering Cancer Center and Weill Cornell School of Medicine, where he leads the Immunogenomics and Precision Oncology Platform and was a tenured professor, the PaineWebber Chair, and the Translational Oncology Division chair. He is an internationally recognized expert in precision immuno-oncology and a pioneer in using genomics to determine which patients will respond best to certain types of immunotherapies. He has published over 200 articles in peer-reviewed journals, has made landmark discoveries in his field, and has received numerous awards, including the National Cancer Institute Outstanding Investigator Award in 2018.

Innovation in precision immunotherapy is one of the most exciting areas in cancer research, said Brian Bolwell, M.D., chairman of Taussig Cancer Institute, Cleveland Clinic Cancer Center. The addition of Dr. Chan, a pioneer in cancer genomics, and the new centers focus on research and clinical trials will strengthen our ability to provide advanced treatment options for our patients.

Dr. Chan also joins the leadership of the National Center for Regenerative Medicine of Case Western Reserve University. Dr. Chan is also on staff in the Genomic Medicine Institute of the Lerner Research Institute; and the Department of Radiation Oncology of the Taussig Cancer Institute.

Dr. Chan earned his M.D. and Ph.D. in genetics from Johns Hopkins University, where he also completed a residency in radiation oncology and a postdoctoral fellowship in the division of tumor biology. He is board certified in radiation oncology and is an elected member of the Association of American Physicians (AAP).

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Cleveland Clinic Appoints Timothy Chan, M.D., Ph.D., as Director of Center for Immunotherapy and Precision Immuno-Oncology - Health Essentials from...

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How Coronavirus Pandemic Will Impact Regenerative Medicine Products Market, Share, Growth, Trends And Forecast To 2026 – Jewish Life News

Posted: April 27, 2020 at 2:49 pm

Analysis of the Global Regenerative Medicine Products Market

The report on the global Regenerative Medicine Products market reveals that the market is expected to grow at a CAGR of ~XX% during the considered forecast period (2019-2029) and estimated to reach a value of ~US$XX by the end of 2029. The latest report is a valuable tool for stakeholders, established market players, emerging players, and other entities to devise effective strategies to combat the impact of COVID-19

Further, by leveraging the insights enclosed in the report, market players can devise concise, impactful, and highly effective growth strategies to solidify their position in the Regenerative Medicine Products market.

Research on the Regenerative Medicine Products Market Addresses the Following Queries

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Competitive Landscape

The competitive landscape section offers valuable insights related to the business prospects of leading market players operating in the Regenerative Medicine Products market. The market share, product portfolio, pricing strategy, and growth strategies adopted by each market player is included in the report. The major steps taken by key players to address the business challenges put forward by the novel COVID-19 pandemic is discussed in the report.

Regional Landscape

The regional landscape section provides a deep understanding of the regulatory framework, current market trends, opportunities, and challenges faced by market players in each regional market. The various regions covered in the report include:

End-User Assessment

The report bifurcates the Regenerative Medicine Products market based on different end users. The supply-demand ratio and consumption volume of each end-user is accurately depicted in the report.

Market Segment AnalysisThe research report includes specific segments by Type and by Application. This study provides information about the sales and revenue during the historic and forecasted period of 2015 to 2026. Understanding the segments helps in identifying the importance of different factors that aid the market growth.Segment by Type, the Regenerative Medicine Products market is segmented intoCell TherapyTissue EngineeringBiomaterialOthers

Segment by ApplicationDermatologyCardiovascularCNSOrthopedicOthers

Global Regenerative Medicine Products Market: Regional AnalysisThe Regenerative Medicine Products market is analysed and market size information is provided by regions (countries). The report includes country-wise and region-wise market size for the period 2015-2026. It also includes market size and forecast by Type and by Application segment in terms of sales and revenue for the period 2015-2026.The key regions covered in the Regenerative Medicine Products market report are:North AmericaU.S.CanadaEuropeGermanyFranceU.K.ItalyRussiaAsia-PacificChinaJapanSouth KoreaIndiaAustraliaTaiwanIndonesiaThailandMalaysiaPhilippinesVietnamLatin AmericaMexicoBrazilArgentinaMiddle East & AfricaTurkeySaudi ArabiaU.A.EGlobal Regenerative Medicine Products Market: Competitive AnalysisThis section of the report identifies various key manufacturers of the market. It helps the reader understand the strategies and collaborations that players are focusing on combat competition in the market. The comprehensive report provides a significant microscopic look at the market. The reader can identify the footprints of the manufacturers by knowing about the global revenue of manufacturers, the global price of manufacturers, and sales by manufacturers during the forecast period of 2015 to 2019.The major players in global Regenerative Medicine Products market include:AcelityDePuy SynthesMedtronicZimmerBiometStrykerMiMedx GroupOrganogenesisUniQureCellular Dynamics InternationalOsiris TherapeuticsVcanbioGamida CellGolden MeditechCytori TherapeuticsCelgeneVericel CorporationGuanhao BiotechMesoblastStemcell TechnologesBellicum Pharmaceuticals

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Essential Findings of the Regenerative Medicine Products Market Report:

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How Coronavirus Pandemic Will Impact Regenerative Medicine Products Market, Share, Growth, Trends And Forecast To 2026 - Jewish Life News

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Pluristem Secures 50 Million Non-Dilutive Financing from the European Investment Bank to Support its COVID-19 Project and Phase III StudiesEXPECTED…

Posted: April 27, 2020 at 2:49 pm

HAIFA, Israel, April 24, 2020 (GLOBE NEWSWIRE) -- Pluristem Therapeutics Inc. (Nasdaq:PSTI) (TASE:PSTI), a leading regenerative medicine company developing a platform of novel biological therapeutic products, announced today that the European Investment Bank (EIB) has approved a 50 million non-dilutive financing for the Company (the Approved Financing). This Approved Financing, once received, will support Pluristems research and development in the EU to further advance its regenerative cell therapy platform, and to assist moving the products in its pipeline to market, with a special focus on clinical development of PLX cells as a treatment for complications associated with COVID-19. The Approved Financing will be deployed in three tranches, subject to the achievement of certain clinical, regulatory and scaling up milestones, with the first tranche consisting of 20 million. The expected signing date of the financing agreement relating to the Approved Financing is April 30, 2020.

Pluristem recently formed a wholly-owned subsidiary in Berlin, Germany, underscoring the Companys commitment to having a physical presence in Europe to advance research and development, and to prepare for commercialization, for its product candidates.

The Approved Financing is backed by a guarantee from the European Fund for Strategic Investments (EFSI), the financial pillar of the Investment Plan for Europe, under which the EIB and the European Commission are working together as strategic partners to boost Europes economic competitiveness. The transaction has been initiated by kENUP Foundation, a global partnership in innovation, promoting research-based innovation for Europe with public and societal benefit.

The Approved Financing, once granted, will not be secured and will be payable to the EIB in a single payment following five years from the disbursement of the first and second tranches and in two annual payments starting on the fourth year from disbursement of the third tranche, with each tranche having an interest rate of between 3% to 4%. The Approved Financing will support up to 50% of Pluristems R&D project cost. In addition, the EIB would be entitled to receive royalties from future revenues for a period of seven years starting 2024, at a rate of 0.2% to 2.3%, pro-rated to the amounts that the Company received from the Approved Financing.

We are extremely honored to have been selected by the EIB for this prestigious financing. We believe that this financing will allow us to significantly advance the clinical development of our lead product candidates, which if successful we expect will improve the quality of life for millions of patients around the world. Having established research partnerships with leading European institutions such as Charit University of Medicine Berlin, BIH Center for Regenerative Therapy (BCRT) and the Berlin Center for Advanced Therapies (BeCAT), as well as formed a subsidiary in Berlin, we understand the importance of having a physical presence in key markets, stated Pluristem CEO and President, Yaky Yanay. As we move forward into a multinational clinical trial for PLX cells to treat patients suffering from complications associated with COVID-19, we expect this EIB financing will accelerate our path to approval and to making a potentially effective COVID-19 treatment available worldwide.

About the European Investment Bank The European Investment Bank (EIB) is the long-term lending institution of the European Union, owned by its Member States. It makes long-term finance available for sound investment in order to contribute towards EU policy goals.

Investment Plan for Europe The Investment Plan for Europe (the Juncker Plan) is one of the EU's key actions to boost investment in Europe, thereby creating jobs and fostering growth. To this end, smarter use will be made of new and existing financial resources. The EIB Group, consisting of the European Investment Bank and the European Investment Fund, is playing a vital role in this investment plan. With guarantees from the European Fund for Strategic Investments (EFSI), the EIB and EIF are able to take on a higher share of project risk, encouraging private investors to participate in the projects. In addition to EFSI, the new European Investment Advisory Hub (EIAH) helps public and private sector project promoters to structure investment projects more professionally. The projects and agreements approved under EFSI (European Fund for Strategic Investments) so far are expected to mobilise almost 466 billion of investments and will benefit over 1 million start-ups and SMEs (Small Medium Enterprises) in the 27 Member States.

About Pluristem TherapeuticsPluristem Therapeutics Inc. is a leading regenerative medicine company developing novel placenta-based cell therapy product candidates. The Company has reported robust clinical trial data in multiple indications for its patented PLX cell product candidates and is currently conducting late stage clinical trials in several indications. PLX cell product candidates are believed to release a range of therapeutic proteins in response to inflammation, ischemia, muscle trauma, hematological disorders and radiation damage. The cells are grown using the Company's proprietary three-dimensional expansion technology and can be administered to patients off-the-shelf, without tissue matching. Pluristem has a strong intellectual property position; a Company-owned and operated GMP-certified manufacturing and research facility; strategic relationships with major research institutions; and a seasoned management team.

Safe Harbor Statement This press release contains express or implied forward-looking statements within the Private Securities Litigation Reform Act of 1995 and other U.S. Federal securities laws. For example, Pluristem is using forward-looking statements when it discusses its expectation that it will execute a definitive agreement for the Approved Financing and the proposed terms of such Approved Financing, the belief that the Approved Financing will support its research and development in the EU to further advance its regenerative cell therapy platform, to assist moving the products in its pipeline to market, with a special focus on clinical development of PLX cells as a treatment for complications associated with COVID-19, that such Approved Financing will allow it to significantly advance its clinical development of its lead product candidates which it expects will improve the quality of life for millions of patients around the world and the expectation that the Approved Financing will accelerate its path to approval of its COVID-19 multinational clinical trial and to making a potentially effective COVID-19 treatment available worldwide. While the EIB has announced the approval of the Approved Financing, there is no guarantee that the Company and the EIB will execute the definitive agreement on April 30, 2020, if at all, or that it will achieve the milestones necessary to receive any or all of the three tranches. These forward-looking statements and their implications are based on the current expectations of the management of Pluristem only, and are subject to a number of factors and uncertainties that could cause actual results to differ materially from those described in the forward-looking statements. The following factors, among others, could cause actual results to differ materially from those described in the forward-looking statements: changes in technology and market requirements; Pluristem may encounter delays or obstacles in launching and/or successfully completing its clinical trials; Pluristems products may not be approved by regulatory agencies, Pluristems technology may not be validated as it progresses further and its methods may not be accepted by the scientific community; Pluristem may be unable to retain or attract key employees whose knowledge is essential to the development of its products; unforeseen scientific difficulties may develop with Pluristems process; Pluristems products may wind up being more expensive than it anticipates; results in the laboratory may not translate to equally good results in real clinical settings; results of preclinical studies may not correlate with the results of human clinical trials; Pluristems patents may not be sufficient; Pluristems products may harm recipients; changes in legislation may adversely impact Pluristem; inability to timely develop and introduce new technologies, products and applications; loss of market share and pressure on pricing resulting from competition, which could cause the actual results or performance of Pluristem to differ materially from those contemplated in such forward-looking statements. Except as otherwise required by law, Pluristem undertakes no obligation to publicly release any revisions to these forward-looking statements to reflect events or circumstances after the date hereof or to reflect the occurrence of unanticipated events. For a more detailed description of the risks and uncertainties affecting Pluristem, reference is made to Pluristem's reports filed from time to time with the Securities and Exchange Commission.

Contact:Dana RubinDirector of Investor Relations+972-74-7107194danar@pluristem.com

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Pluristem Secures 50 Million Non-Dilutive Financing from the European Investment Bank to Support its COVID-19 Project and Phase III StudiesEXPECTED...

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Regenerative Medicine Products Market Overview, Top Companies, Region, Application and Global Forecast by 2026 – Latest Herald

Posted: April 27, 2020 at 2:49 pm

Bellicum Pharmaceuticals

Global Regenerative Medicine Products Market Segmentation

This market was divided into types, applications and regions. The growth of each segment provides an accurate calculation and forecast of sales by type and application in terms of volume and value for the period between 2020 and 2026. This analysis can help you develop your business by targeting niche markets. Market share data are available at global and regional levels. The regions covered by the report are North America, Europe, the Asia-Pacific region, the Middle East, and Africa and Latin America. Research analysts understand the competitive forces and provide competitive analysis for each competitor separately.

To get Incredible Discounts on this Premium Report, Click Here @ https://www.marketresearchintellect.com/ask-for-discount/?rid=222856&utm_source=LHN&utm_medium=888

Regenerative Medicine Products Market Region Coverage (Regional Production, Demand & Forecast by Countries etc.):

North America (U.S., Canada, Mexico)

Europe (Germany, U.K., France, Italy, Russia, Spain etc.)

Asia-Pacific (China, India, Japan, Southeast Asia etc.)

South America (Brazil, Argentina etc.)

Middle East & Africa (Saudi Arabia, South Africa etc.)

Some Notable Report Offerings:

-> We will give you an assessment of the extent to which the market acquire commercial characteristics along with examples or instances of information that helps your assessment.

-> We will also support to identify standard/customary terms and conditions such as discounts, warranties, inspection, buyer financing, and acceptance for the Regenerative Medicine Products industry.

-> We will further help you in finding any price ranges, pricing issues, and determination of price fluctuation of products in Regenerative Medicine Products industry.

-> Furthermore, we will help you to identify any crucial trends to predict Regenerative Medicine Products market growth rate up to 2026.

-> Lastly, the analyzed report will predict the general tendency for supply and demand in the Regenerative Medicine Products market.

Have Any Query? Ask Our Expert@ https://www.marketresearchintellect.com/need-customization/?rid=222856&utm_source=LHN&utm_medium=888

Table of Contents:

Study Coverage: It includes study objectives, years considered for the research study, growth rate and Regenerative Medicine Products market size of type and application segments, key manufacturers covered, product scope, and highlights of segmental analysis.

Executive Summary: In this section, the report focuses on analysis of macroscopic indicators, market issues, drivers, and trends, competitive landscape, CAGR of the global Regenerative Medicine Products market, and global production. Under the global production chapter, the authors of the report have included market pricing and trends, global capacity, global production, and global revenue forecasts.

Regenerative Medicine Products Market Size by Manufacturer: Here, the report concentrates on revenue and production shares of manufacturers for all the years of the forecast period. It also focuses on price by manufacturer and expansion plans and mergers and acquisitions of companies.

Production by Region: It shows how the revenue and production in the global market are distributed among different regions. Each regional market is extensively studied here on the basis of import and export, key players, revenue, and production.

About Us:

Market Research Intellect provides syndicated and customized research reports to clients from various industries and organizations with the aim of delivering functional expertise. We provide reports for all industries including Energy, Technology, Manufacturing and Construction, Chemicals and Materials, Food and Beverage and more. These reports deliver an in-depth study of the market with industry analysis, market value for regions and countries and trends that are pertinent to the industry.

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Mr. Steven Fernandes

Market Research Intellect

New Jersey ( USA )

Tel: +1-650-781-4080

Tags: Regenerative Medicine Products Market Size, Regenerative Medicine Products Market Growth, Regenerative Medicine Products Market Forecast, Regenerative Medicine Products Market Analysis

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Regenerative Medicine Market Segmentation, Application, Technology, Analysis Research Report and Forecast to 2026 – Cole of Duty

Posted: April 27, 2020 at 2:49 pm

Stryker Corporation and NuVasive

Global Regenerative Medicine Market Segmentation

This market was divided into types, applications and regions. The growth of each segment provides an accurate calculation and forecast of sales by type and application in terms of volume and value for the period between 2020 and 2026. This analysis can help you develop your business by targeting niche markets. Market share data are available at global and regional levels. The regions covered by the report are North America, Europe, the Asia-Pacific region, the Middle East, and Africa and Latin America. Research analysts understand the competitive forces and provide competitive analysis for each competitor separately.

To get Incredible Discounts on this Premium Report, Click Here @ https://www.verifiedmarketresearch.com/ask-for-discount/?rid=7157&utm_source=COD&utm_medium=005

Regenerative Medicine Market Region Coverage (Regional Production, Demand & Forecast by Countries etc.):

North America (U.S., Canada, Mexico)

Europe (Germany, U.K., France, Italy, Russia, Spain etc.)

Asia-Pacific (China, India, Japan, Southeast Asia etc.)

South America (Brazil, Argentina etc.)

Middle East & Africa (Saudi Arabia, South Africa etc.)

Some Notable Report Offerings:

-> We will give you an assessment of the extent to which the market acquire commercial characteristics along with examples or instances of information that helps your assessment.

-> We will also support to identify standard/customary terms and conditions such as discounts, warranties, inspection, buyer financing, and acceptance for the Regenerative Medicine industry.

-> We will further help you in finding any price ranges, pricing issues, and determination of price fluctuation of products in Regenerative Medicine industry.

-> Furthermore, we will help you to identify any crucial trends to predict Regenerative Medicine market growth rate up to 2026.

-> Lastly, the analyzed report will predict the general tendency for supply and demand in the Regenerative Medicine market.

Have Any Query? Ask Our Expert @ https://www.verifiedmarketresearch.com/product/global-regenerative-medicine-market/?utm_source=COD&utm_medium=005

Table of Contents:

Study Coverage: It includes study objectives, years considered for the research study, growth rate and Regenerative Medicine market size of type and application segments, key manufacturers covered, product scope, and highlights of segmental analysis.

Executive Summary: In this section, the report focuses on analysis of macroscopic indicators, market issues, drivers, and trends, competitive landscape, CAGR of the global Regenerative Medicine market, and global production. Under the global production chapter, the authors of the report have included market pricing and trends, global capacity, global production, and global revenue forecasts.

Regenerative Medicine Market Size by Manufacturer: Here, the report concentrates on revenue and production shares of manufacturers for all the years of the forecast period. It also focuses on price by manufacturer and expansion plans and mergers and acquisitions of companies.

Production by Region: It shows how the revenue and production in the global market are distributed among different regions. Each regional market is extensively studied here on the basis of import and export, key players, revenue, and production.

About us:

Verified market research partners with the customer and offer an insight into strategic and growth analyzes, Data necessary to achieve corporate goals and objectives. Our core values are trust, integrity and authenticity for our customers.

Analysts with a high level of expertise in data collection and governance use industrial techniques to collect and analyze data in all phases. Our analysts are trained to combine modern data collection techniques, superior research methodology, expertise and years of collective experience to produce informative and accurate research reports.

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Tags: Regenerative Medicine Market Size, Regenerative Medicine Market Trends, Regenerative Medicine Market Growth, Regenerative Medicine Market Forecast, Regenerative Medicine Market Analysis

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Regenerative Medicine Market Segmentation, Application, Technology, Analysis Research Report and Forecast to 2026 - Cole of Duty

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NFL Alumni Providing COVID-19 Rapid Antibody Screening Tests by Teaming Up With 1271 Partners, Streamline Medical Group, and RayBiotech – PRNewswire

Posted: April 27, 2020 at 2:49 pm

MOUNT LAUREL, N.J., April 23, 2020 /PRNewswire/ --1271 Partners, Streamline Medical Group, and RayBiotech have partnered to provide COVID-19 testing to the NFL Alumni Association and its members. The partnership is offering Coronavirus (COVID-19) IgM/IgG Dual Antibody Rapid Test Kits as a member benefit to NFL Alumni members with telemedicine consultations to help families screen and possibly prevent the spread of the virus.

1271 Partners and Streamline Medical Group have executed a distribution agreement that provides an exclusive license to provide RayBiotech's IgM/IgG Dual Antibody Rapid Test Kits to all of the professional sports leagues and arenas, such as the NFL, NBA, MLB, etc. In addition, 1271 Partners and Streamline can distribute the Rapid Test Kits in North America, South America, and Europe on a non-exclusive basis.

"As an ongoing effort to fight the COVID-19 crisis we are fortunate to offer, our members and NFL Alumni families,an option for a rapid screening test, thanks toRayBiotech, 1271 Partners and Streamline Medical Group's relationships," said NFLA CEO Beasley Reece.

"Streamline Medical Group has always been on the forefront of optimal health and wellness through our blood testing for our patients. Streamline now has the opportunity to address the emergency need for valid COVID-19 rapid screening in partnership with the NFL Alumni Association Athletica and 1271 Partners," says Gary Brecka, CEO of Streamline Medical Group. "Along with 1271 Partners, we chose to become a distribution partner with RayBiotech because of their location right here in the USA and their history of providing cutting-edge array technologies for the discovery of regenerative medicine and disease-related protein biomarkers. We have a very high degree of confidence in their testing capabilities."

"As a managing member of 1271 Partners and a fellow NFL Alumnus, I am more than thrilled to offer our constituents, families and consumers-at large through the NFL Alumni Athletica platform, the opportunity to distribute COVID-19 Rapid Test Kits manufactured right here in the U.S. We are all living in challenging times and to provide a quick solution for some peace of mind is very satisfying," said 1271 Partners Managing Member, Billy Davis.

"We are very excited to partner with this excellent group of organizations to help provide access to COVID-19 screening kits for its members, the sporting community, all the fans and businesses that surround them. Specifically having the ability to work with the NFL Alumni and the 35 chapters throughout the country, will provide a gateway of solutions not only for the Alumni members but also the consumers and local businesses trying to get back to work in a safe and effective manner,"said RayBiotech Senior Business Development Manager, Jarad Wilson.

About NFL Alumni:NFL Alumni, a non-profit organization founded in 1967, is comprised of former NFL players, coaches, staffers, cheerleaders, spouses, and associate members whose mission is to serve, assist and inform former players and their families. The NFL Alumni offers a variety of medical, financial, and social programs to help members lead healthy, productive and connected lives, as well as community initiatives under its "Caring for Kids" programs. Pro Football Legends is the commercial marketing arm of the NFL Alumni. For more information, please visitwww.nflalumni.org.

About 1271 Partners:1271 Partners LLC is the managing entity for the NFL Alumni Athletica. Empowering healthcare consumers with leading scientific, evidence-based treatment options. The same standards of medical care received by elite and professional athletes should be made available to all. 1271 Partners LLC is a premier distributor of tissue and medical device products to the healthcare markets. We have deep experience in sales, operations, and logistics to lead the industry in effectively innovating in order to serve evolving market demands.

About Streamline Medical Group:Streamline Medical Group, along with Streamline Wellness, an organization with anti-aging and regenerative medicine clinics across the U.S., is focused on empowering patients to take control of their health and wellness to help them reach optimal wellness and reduce their healthcare costs. Streamline bases its personalized treatment protocols on each patient's unique biomarkers and prescribes a variety of products and services to help that patient reach their health and wellness goals. Streamline's ability to educate and empower the patient is enhanced with its proprietary report called the Streamline360 that simply explains how each biomarker ties in to specific bodily functions and, when optimized, how that correlates to optimal wellness. For more information, please visithttps://www.streamlinewellness.com

About RayBiotech:RayBiotech is a leading life sciences company providing proteomic discovery tools. RayBiotech has nearly 150 employees whose objectives are to provide excellent products and service worldwide to RayBiotech customers which include scientists in industry, academic and research institutes in over 41 countries. RayBiotech is committed to accelerating customer success through innovation and leadership in the Life Sciences. For more information, please visithttps://www.raybiotech.com

MEDIA CONTACT:Benjamin LeeStreamline Medical Group561.628.8488[emailprotected]

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SOURCE National Football League Alumni Association

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NFL Alumni Providing COVID-19 Rapid Antibody Screening Tests by Teaming Up With 1271 Partners, Streamline Medical Group, and RayBiotech - PRNewswire

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Healing the heart by returning it to its infancy – FierceBiotech

Posted: April 27, 2020 at 2:49 pm

Nearly a decade ago, researchers at UT Southwestern Medical Center discovered that when mouse hearts were damaged in the first seven days of life, they would regenerate. They reasoned that if they could find a way to recreate that regenerative ability later in life, it might provide a new way to treat heart damage.

Now, that same team has discovered that a protein called calcineurin plays a key role in blocking the ability of heart muscle to regenerate after the first week of life. The discovery could be used to develop treatments that reverse this process, in essence returning the heart to its developmental stage, they reported in the journal Nature.

The discovery builds on previous work at UT Southwestern that focused on the protein Meis1, a transcription factor that prevents heart cells from dividing. When the researchers deleted the gene in mice that makes that protein, their cardiomyocytes continued to divide after the first week of life. But the effect was transient.

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RELATED: Stem cells don't repair injured hearts, but inflammation might, study finds

Then the researchers discovered that another protein called Hoxb13 was also key, because it shuttles Meis1 into the cell nucleus. So they deleted the genes for both Meis1 and Hoxb13 in adult mice to see what would happen after a heart attack.

It worked. The ability of the animals hearts to pump blood quickly returned to near-normal levels, they said. Even though the mice were adults, their hearts looked much like they would in animals that were still developing.

After a series of further experiments, the UT Southwestern scientists discovered that calcineurin regulates both Hoxb13 and Meis1. Inhibiting calcineurin prolongs the window of cardiomyocyte proliferation, they wrote in the study.

The idea of treating heart damage by turning back the clock isnt new. In fact, several research teams have tried using stem cells to repair damaged heart tissue. But those efforts have been disappointing so far.

Last year, a team from the Cincinnati Children's Hospital Medical Center tracked stem cells injected into the hearts of mice and concluded that it was not the cells themselves, but rather their ability to activate macrophage cells from the immune system that promoted healing. That led the researchers to suggest that efforts to regenerate the heart focus less on stem cells and more on other processes in the body that might promote healing.

The discovery of calcineurins role in regulating the regeneration of the heart is notable due to the fact that there are already drugs on the market that target the protein. Thats because calcineurin plays a role in a variety of diseases, including rheumatoid arthritis and diabetes. Testing these drugs, either individually or in combination, and developing new medicines that target calcineurin directly could offer new strategies for repairing hearts damaged by heart attacks, high blood pressure, viruses and more, suggested co-author Hesham Sadek, M.D., Ph.D., a professor of internal medicine, molecular biology and biophysics at UT Southwestern.

"By building up the story of the fundamental mechanisms of heart cell division and what blocks it, Sadek said in a statement, we are now significantly closer to being able to harness these pathways to save lives.

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Healing the heart by returning it to its infancy - FierceBiotech

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Science Becomes A Dividing Issue In Year Of Election And Pandemic – Wyoming Public Media

Posted: April 27, 2020 at 2:48 pm

It now seems apparent that COVID-19 will dominate American life for months to come, quite possibly through the national election in November.

That means the disease, and efforts to respond to it, will likewise dominate the 2020 campaign and make it largely about something it has never been about before.

That something is science.

It is hard to think of a time when hard science biology, virology, epidemiology has been so much the core of our political conflict. Issues from evolution to stem cells to vaccination have long been a part of our political conversation, but not at the forefront of presidential elections.

This virus crisis has largely taken over the political conversation. Americans are all learning new, polysyllabic vocabulary and complex truths about threats they cannot see.

And that is likely to bring out all of the culture's ambivalence about science.

Trust in science

Last summer, a Pew Research Center survey found that 86% of Americans expressed "a fair amount or a great deal of faith" that scientists act in their best interests.

But the survey's co-author told NPR, "It tends to be kind of soft support." In fact, only 48% were willing to say that medical doctors "make fair and accurate research statements and recommendations all or most of the time." And only 32% were willing to say as much for "medical research scientists."

A YouGov poll in April 2017 found an even less sanguine attitude, as reported in Scientific American. That measure found only 35% of Americans had "a lot of confidence" in scientists. A plurality (45%) had "a little," while those with "none at all" had grown substantially since YouGov polled the same question in 2013.

Little wonder then that political figures such as Texas Lt. Gov. Dan Patrick, a Republican, and media personalities such as Fox News' Tucker Carlson pounce on the difference between various projections of deaths from COVID-19.

They interpret lower death totals (thus far) as evidence that the threat was overblown, even though public health experts consider it proof that shutdowns and social distancing are working and note that the threat is not over.

Rejecting expertise

Scientific experts, like experts in general, have fared poorly in the populist atmosphere of the past decade in Europe and the United States.

"Voters say they reject expertise because experts, whom they think of as indistinguishable from governing elites, have failed them," writes Tom Nichols, a professor of national security affairs at the U.S. Naval War College.

Nichols published a book in 2017 called The Death of Expertise: The Campaign Against Established Knowledge and Why It Matters. Summing up his argument for Politico, Nichols observed that Americans have always had a healthy skepticism about "eggheads" of various kinds.

He says that skepticism renewed itself in the "social and political traumas" of the 1960s and 1970s. But since then, he argues, "Globalization and technological advances have created a gulf between people with enough knowledge and education to cope with these changes and people who feel threatened and left behind in the new world of the 21st century."

Lacking "scientific merit"

The plain fact is that for many, science is a source of wisdom but by no means the only one. There can be a "balancing" of science with religious teaching or humanistic ethics or what people may regard as their own common sense.

That is why so many Americans may identify with President Trump's overeagerness about potential drug therapies for COVID-19 that have worked on other diseases.

Trump's hopefulness for the antimalarial hydroxychloroquine, for example, was apparently not shared by one of the administration's own leading vaccine scientists, Richard Bright. Bright tried to limit broad use of the drug because its application lacked "scientific merit." As a result, he says, he was removed as director of the Biomedical Advanced Research and Development Authority.

In a statement released by his attorneys last week, Bright sounded the alarm: "To combat this deadly virus, science, not politics or cronyism, has to lead the way."

Also this past week, the president stood at the podium of the White House briefing room and cast doubt on the survival of the coronavirus in the fall. He then deferred to his top scientific adviser on the question.

"We will have the virus in the fall," said Dr. Anthony Fauci of the National Institutes of Health.

Trump also insisted the head of the Centers for Disease Control and Prevention had been misquoted about the difficulties of managing COVID-19 in the fall. Dr. Robert Redfield took the lectern to say he had not been misquoted.

But all this was prelude to the Thursday night stunner, when the president extended his embrace of "game-changer" therapy ideas to raising the question of whether injecting a disinfectant (which can kill the coronavirus on a surface) into a person could kill the virus (in reality, doing so would be toxic).

This prompted such immediate blowback from scientists, hospital personnel and even the makers of Lysol that the president later insisted he had made the comment sarcastically. And the next evening's briefing was cut off at just 22 minutes, with the president taking no questions.

A long-term struggle

The crisis is spreading through the body politic even as it spreads through the human population. It will stress both in myriad ways. Americans' conflicted relationship with science will play a role in how they deal with that stress.

For the moment, most are accepting the scientific approach of social distancing in service of a greater good. But there are rejections of stay-at-home orders in street protests and in some statehouses.

Saturday night, Trump repeated a line used to argue for reopening the country sooner rather than later: "Remember, the Cure can't be worse than the problem itself." He added, "Be careful, be safe, use common sense!"

The struggle has been joined, and it will likely outlast both this one campaign season and this one pandemic.

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Q&A on COVID-19 Antibody Tests – FactCheck.org

Posted: April 27, 2020 at 2:47 pm

Much of the focus on COVID-19 testing thus far into the pandemic has been on tests that can determine whether someone is actively infected with the novel coronavirus, or SARS-CoV-2. But, in his drive to open up America again, President Donald Trump has turned his attentionto blood-based antibody tests, which can show whether someone was previously infected with the virus.

This will help us assess the number of cases that have been asymptomatic or mildly symptomatic, and support our efforts to get Americans back to work by showing us who might have developed the wonderful, beautiful immunity, Trump said at anApril 17 press conference.

The tests do have the potential to relay valuable information about who might already have immunity and how widely COVID-19 has spread. But so far, the tests are not widely available and many of those that are available do not work as advertised.

The U.K., for instance, spent $20 million on antibody tests from China that the government subsequently found were not accurate enough to use. An emergency room in Laredo, Texas, also dropped half a million dollars on tests from China that were too unreliable to deploy.

Other tests are better but, like any test, will still miss some people who have antibodies or incorrectly tag others as having antibodies when they dont. And more fundamentally, experts told us too little is known about how the immune system responds to the new virus to know for sure whether antibodies actually protect a person from contracting the disease.

Well run through how the tests work and why its so hard to interpret what the results might mean.

What are antibodies and why is it useful to check for them?

Antibodies are specialized proteins that help clear the body of invading microbes. Made by immune cells known as B cells shortly after infection, antibodies specifically recognize pathogens, binding to the surfaces of viruses and stopping them from entering cells, for example, or marking them for destruction by other parts of the immune system.

The proteins dont exist until at least a few days into an acute infection, and often arent detectable until a week or more after symptoms appear, Rangarajan Sampath, the chief scientific officer of the nonprofit Foundation for Innovative New Diagnostics, told us.

But because some antibodies persist for months if not years after someone has recovered, they offer a glimpse into the past and can reveal whether someone was previously infected, potentially even if that person never had symptoms.

The earliest antibodies that B cells pump out known as immunoglobulin M, or IgM may overlap with infection, Sampath said. IgM antibodies bind a bit less well to pathogens, but are the first on the scene, peaking within several weeks or so andthen declining. The most common antibody, IgG, takes longer to ramp up, but is more finely tuned to recognize microbes and is longer-lasting. Other antibody types, including IgA, which is present in the respiratory tract, are also delayed.

Because of the time lag, antibody tests are not very good at determining whether someone is infected with SARS-CoV-2.

The antibody test by itself cannot tell you whether youre currently active with a live infection or not, said Sampath. You could be. You cannot rule it out. But its also possible that what you had was a past infection, as recently as a few days ago.

For this reason, the Food and Drug Administration says antibody tests should not be used as the sole basis to diagnose COVID-19. Molecular tests, which check for the presence of viral RNA, are needed to diagnose an infection.

Its worth mentioning that different antibodies have different functions, and most antibody tests cannot discriminate between those that may be able to bind to the virus, but arent able to prevent infection the way so-called neutralizing antibodies can.

These tests are just looking for the presence of antibodies that are able to recognize SARS-CoV-2, said Lisa Gralinski, a virologist who studies human coronaviruses at the University of North Carolina at Chapel Hill. Theyre not telling us anything about the quality of those antibodies, so we dont know if theyre neutralizing.

Usually we would expect that they are, but in the case of an ongoing pandemic, she added, we dont want to be providing people with false confidence or incorrect information.

This is one reason why health experts have been cautious about making sweeping claims that antibody tests can necessarily identify those who are immune, even if scientists think its highly likely that a person with antibodies will have at least partial immunity for some period of time.

In the context of the current pandemic, a persons antibodies may also be valuable as a possible COVID-19 treatment. Scientists are exploring delivering antibody-rich blood, or whats called convalescent plasma, from people who recovered from COVID-19 to help patients still struggling with the disease.

How do COVID-19 antibody tests work?

Precisely because antibodies are highly specific and bind to certain features of a pathogen for example, the spike protein that sticks out from the surface of the COVID-19 virus its possible to design tests that can fish them out and say whether a person has them in their blood. (Antibody tests are also known as serological tests, since antibodies are found in the serum portion of the blood.)

As Johns Hopkins Center for Health Security explains, this can be done in the lab with whats called an enzyme-linked immunosorbent assay, or ELISA. Scientists attach some SARS-CoV-2 surface protein to a plastic plate, then add a bit of patient serum. If there are antibodies in the serum that recognize the viruss surface protein, they will stick to the protein, which can then be seen by adding a lab antibody that recognizes human antibodies and has the ability to trigger a color change.

Other tests try to do something similar, but in a more user-friendly platform. Many rapid serology tests, for instance, look a bit like pregnancy tests, but instead of using a urine sample, require the user to add a small amount of blood. As the liquid moves through the test strip, SARS-CoV-2 antibodies, if present, encounter viral proteins, and can even be sorted according to whether they are IgM or IgG, with a positive result popping up as a colored band.

The rapid tests typically take 10-30 minutes per sample, whereas the lab-based ELISAs take several hours, but can test many samples at once.

How accurate are COVID-19 antibody tests?

Poor accuracy has plagued many of the first tests that companies developed. Sampath said the problems boil down to bad reagents, or the materials the tests use, and a general lack of validation to know whether the tests work.

Many of the tests that came out initially came out in a hurry, he said. And many of them were not tested widely. They were tested on a very small set of, lets say, highly positive patients that may have looked like this was really good. But now, when you start testing them on a broader population, you start finding that they didnt really have the performance that was needed.

One issue, Sampath said, is that some tests, especially the rapid ones, may be falsely detecting antibodies to other coronaviruses, including those that cause common colds. That could yield a high false positive rate, which could be dangerous if people are led to believe they might be immune. Tests, too, may not be sensitive enough to detect SARS-CoV-2 antibodies when they are present, producing false negatives.

Indeed, the two measures that dictate how reliable a test is are sensitivity, or how many people are correctly labeled as having antibodies, and specificity, or how many people are correctly told they lack them.

Many manufacturers report these figures based on small-scale, in-house tests, but those reports may not reflect reality on the ground, as some governments have found.

In one preliminary evaluation, posted as a preprint to medRxiv, nine commercially available rapid tests were found to miss as many as 35% to 45% of samples that were positive. The rapid tests generally produced fewer false positives 7% or less but even that performance may not be good enough, especially if the tests are used in a population in which few people have been infected.

This gets at a strange quirk of testing, in which test performance depends not just on the quality of the test, but also on the population its being tested in. A test thats 95% specific, for example, might sound pretty good, but if only 1% of people are infected, then 85% of the positive results could be wrong.

Sampaths organization, FIND, is working on independently evaluating a variety of antibody tests. The FDA is also partnering with the Centers for Disease Control and Prevention and the National Institutes of Health to assess serological tests. According to a CDC website, results are expected in late April.

Sampath, however, said he thought it would still be several months before there would be enough data on tests used for patient management. And until then, many bad tests are still out there. Many of those tests are still circulating, he said, and many of them continue to add to this noise and confusion.

Whats the status of COVID-19 antibody tests in the U.S.?

For most people, antibody tests are not yet available, although numerous companies are now making them, and some cities are beginning to roll out tests to determine how many people in the community have already been infected.

As of April 24, the FDA has given emergency use authorization, or EUA, to four antibody tests, including a point-of-care cartridge test from Cellex, a lab-based ELISA from Mount Sinai and a high-throughput test from Ortho Clinical Diagnostics.

Many more antibody tests are on the market, but have not received an EUA. The FDA permits this under a special emergency policy, as long as the test is validated by the manufacturer and test results do not claim the ability to diagnose COVID-19. At this time, the FDA does not allow any serological tests to be performed at home, so all tests must be conducted in clinical labs or by health care workers.

One such non-EUA test is from Abbott, which runs on existing machines in hospitals and reference labs, and has been mentioned by name by the president. The company has said it expects to be able to ship 4 million tests by the end of April and 20 million tests per month, starting in June.

Experts, however, are skeptical that companies will be able to meet the demand for serological tests anytime soon. Were really entering into this era of antibody testing, and were not anywhere close to where we need to be, said Michael Mina, an epidemiologist at Harvard Universitys T.H. Chan School of Public Health, in a press call. Its really going to make the demand for PCR testing look minimal, he added, referring to the molecular diagnostic tests for COVID-19.

Sampath also warned that none of the tests had been fully vetted yet. Even the EUA, its a really quick and dirty way of getting something in front of the FDA for an evaluation. Its not a true FDA-approved test that they would normally do.

And while some of the tests may work fine, Sampath said there was too little data to go on.

There are perhaps a handful of tests that may be on the border of being good enough, but we dont know, he said. And we dont know that because we only have the manufacturers claim.

Will someone be protected from being infected again if they have antibodies to the virus?

Its quite likely that someone with SARS-CoV-2 antibodies will have some degree of immunity to the virus because its a sign the body has seen and responded to the pathogen before and because its typical of most viruses that spark short-term infections.

Generally we know with infections like this, that at least for a reasonable period of time, youre going to have antibody levels that will be protective, said Anthony Fauci, director of the National Institute of Allergy and Infectious Diseases, in an April 8 interview with the Journal of the American Medical Association.

Scientists nevertheless caution that protection is not a given. UNCs Gralinski said immunity would be very likely, but because the virus is new and there isnt direct evidence yet it cant be known for certain.

The World Health Organization also warned against assuming antibodies confer immunity to the virus. Noting in an April 24scientific brief that there has yet to be any study showing that antibodies to SARS-CoV-2 prevent a second infection in humans, the group advised against policies that use antibody tests to identify individuals with immunity.

At this point in the pandemic, there is not enough evidence about the effectiveness of antibody-mediated immunity to guarantee the accuracy of an immunity passport or risk-free certificate,' the WHO said. People who assume that they are immune to a second infection because they have received a positive test result may ignore public health advice. The use of such certificates may therefore increase the risks of continued transmission.

Reports out of South Korea and other parts of Asia have raised concerns about reinfection or viral reactivation a term usually reserved for when viruses go dormant inside cells since some people who recovered from COVID-19 have tested positive again for the virus.

But many scientists are doubtful of those claims. Gralinski said coronaviruses dont reactivate, and rather than people becoming reinfected, its more likely that as patients eliminate the virus from their bodies, the amount of swabbed virus hovers around the diagnostic tests threshold of detection.

My suspicion is that were dealing with sensitivity issues, where people are kind of on the low edge of detectability with their infection as theyre clearing virus, she said. When theyre dancing around the detection limit for virus positivity, its easy to have things go down for a couple of days and then come back up.

Many other questions about potential COVID-19 immunity remain, including what antibody level might be needed to confer protection and whether people who were infected with SARS-CoV-2 but never developed symptoms are any less protected than those with more severe cases.

How long might someone be immune to COVID-19?

Scientists cant know with any certainty how long someone who contracted COVID-19 might be protected, but they can look to other human coronaviruses for clues.

In one experiment, volunteers were intentionally infected with a coronavirus that causes a common cold, and after a year, some participants were susceptible to infection again, although many did not develop noticeable symptoms.

Other studies of patients infected with severe acute respiratory syndrome, or SARS, in 2003 indicate antibodies begin to wane after about four months, but stick around in most people for two years. By year three, though, up to a quarter of patients no longer had detectable antibodies, and after six years,almost noone did.

If SARS-CoV-2 behaves like its predecessor, Gralinski said it might be possible to expect perhaps a couple of years of immunity, but not much more.

Reasonable guesses are that on the short end there might be partial protection for about a year or close to a year. And on the long end it might be longer it might be several years of good protection, said Marc Lipsitch, an epidemiologist and director of Harvards Center for Communicable Disease Dynamics, in a call with reporters. But its really speculative at this point.

Its worth noting that immune protection doesnt just stem from circulating antibodies, nor is it a simple on or off switch. As Vineet Menachery, a coronavirus researcher at the University of Texas, explained in a Twitter thread, there are other ways the body remembers the pathogens it has encountered. This includes so-called memory cells that can swing into action more quickly if a microbe returns. So, even if a person loses their neutralizing antibodies to SARS-CoV-2 and can become reinfected, theyre likely to at least be less sick the second time around.

What do antibody studies say so far about how much COVID-19 has spread?

In the U.S., a few so-called serosurvey or seroprevalence studies are beginning to be done that get at how many people in certain areas have already been infected.

Many of the results, however, are highly preliminary or lack sufficient detail for scientists to fully understand them.

New York state, for example, announced on April 23 that of its first phase of 3,000 antibody tests, 13.9% were positive, with a higher 21.2% positive rate in New York City.

A small survey of 200 people in Chelsea, Massachusetts, found that 64 people, or 32%, tested positive for SARS-CoV-2 antibodies.

Another study, in Santa Clara, California, estimated that 2.5% to 4.2% of all people in the county had been infected with COVID-19, and suggested that the number of COVID-19 cases could be some 50 to 85 times higher than the confirmed count.

The Santa Clara work, however, which has not yet been peer-reviewed and was posted to the preprint site medRxiv, has been heavily criticized for its data analysis and its methodology. Critics argue the population sample, which was recruited from Facebook, may have been biased, and that statistically, the researchers cant actually rule out that all of the positive antibody tests were false positives.

Experts say its important that these studies be done, but some are worried that they are not being done carefully enough. As A. Marm Kilpatrick, a professor at the University of California, Santa Cruz who studies infectious disease dynamics, said on Twitter of the Santa Clara study, We need these kinds of studies and data badly. Unfortunately this paper is badly misleading.

Part of the reason why its so important is because the information can be used to make a more accurate estimate of how dangerous COVID-19 is. If far more people have been infected than expected, that would lower estimates of how deadly COVID-19 is, which could influence public policy decisions about how important it is to keep instituting stringent physical distancing and other public health measures.

The other main reason to keep tabs on the figure is because it can say how close a community might be to achieving herd immunity, or the point at which people who are susceptible to the virus can still be protected because so many other people around them are already immune. This is based on how contagious a disease is, and since people with SARS-CoV-2 infect an average of two to three other people, youd need around 50% to 67% of the population to be immune to get herd immunity.

No results yet indicate any population is close to that. And in fact, most studies from around the world have suggested relatively few people have contracted COVID-19.

As the WHO noted on April 20, many studies indicate only 2% to 3% of people have been infected.

We absolutely must remain vigilant because what were learning fromthese early serologic studies, even with all of their faults and all of the limitations, said WHO scientist Maria Van Kerkhove, is that a lower proportion of people are actually, it appears, are infected. And that means a large proportion of the public remains susceptible.

Update, April 27: We updated the article to include a scientific briefing released by the WHO.

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Coronavirus Doctors experiment with stem cell therapy on COVID-19 patients CBS News 9:39 AM – KTVQ Billings News

Posted: April 26, 2020 at 8:45 am

Doctors are hoping stem cell therapy could be a weapon in the fight against coronavirus. On Friday, regenerative medicine company Mesoblast announced a 300-person trial to determine whether stem cell treatments will work in COVID-19 patients suffering from severe lung inflammation.

One hospital in New York tried it as an experiment with 12 patients, 10 of whom were able to come off of ventilators.

"What we saw in the very first patient was that within four hours of getting the cells, a lot of her parameters started to get better," Dr. Karen Osman, who led the team at Mount Sinai, told CBS News' Adriana Diaz.

The doctor said she was encouraged by the results, though she was hesitant to link the stem cell procedure to her patients' recovery.

"We don't know" if the 10 people removed from ventilators would not have gotten had they not gotten the stem cells, she said. "And we would never dare to claim that it was related to the cells."

She explained that only a "randomized controlled trial" would be the only way "to make a true comparison."

Luis Naranjo, a 60-year-old COVID-19 survivor, was one of Mount Sinai's stem cell trial success stories. He told Diaz in Spanish that he was feeling "much better."

Naranjo's daughter, Paola, brought him to the emergency room, fearful she would not see her father again. Like so many families struck by the coronavirus, she was not allowed inside with him.

"I forgot to tell him that I love him," she said. "All I said was go inside, I hope you feel better."

During his hospital stay, Naranjo was unconscious and on a ventilator for 14 days.

Doctors proposed giving him stem cells from bone marrow in hopes it would suppress the severe lung inflammation caused by the virus.

Now, Naranjo credits the doctors who treated him for his survival. Though income from his family's jewelry business has been cut off and they found themselves falling behind on rent, Naranjo said he is focused primarily on his recovery and regaining the 25 pounds he lost at the hospital.

Although stem cell treatment, usually reserved for other diseases like rheumatoid arthritis, might end up being another step toward helping coronavirus patients recover, Dr. Osman was quick to say it would not be a "miracle treatment."

"The miracle treatment will be a vaccine," she said.

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