Special Issue: The Year in Cognitive Neuroscience (vol 1464) – The New York Academy of Sciences

REVIEWS

The present and future use of functional nearinfrared spectroscopy (fNIRS) for cognitive neuroscience

Paola Pinti, Ilias Tachtsidis, Antonia Hamilton, Joy Hirsch, Clarisse Aichelburg, Sam Gilbert, Paul W. Burgess

Models, movements, and minds: bridging the gap between decision making and action

Nathan J. Wispinski, Jason P. Gallivan, Craig S. Chapman

Recent evidence that attention is necessary, but not sufficient, for conscious perception

Sean Noah, George R. Mangun

Between persistently active and activitysilent frameworks: novel vistas on the cellular basis of working memory

Jan Kamiski, Ueli Rutishauser

Challenging the neurobiological link between number sense and symbolic numerical abilities

Eric D. Wilkey, Daniel Ansari

Musical anhedonia and rewards of music listening: current advances and a proposed model

Amy M. Belfi, Psyche Loui

The intersection between the oculomotor and hippocampal memory systems: empirical developments and clinical implications

Jennifer D. Ryan, Kelly Shen, ZhongXu Liu

Allocentric representations for target memory and reaching in human cortex

Ying Chen, J. Douglas Crawford

Ovarian hormones: a long overlooked but critical contributor to cognitive brain structures and function

Adriene M. Beltz, Jason S. Moser

The importance of diversity in cognitive neuroscience

Vonetta M. Dotson, Audrey Duarte

A new look at the cognitive neuroscience of video game play

Gillian Dale, Augustin Joessel, Daphne Bavelier, C. Shawn Green

Inhibition in selective attention

Dirk van Moorselaar, Heleen A. Slagter

Beyond the feedforward sweep: feedback computations in the visual cortex

Gabriel Kreiman, Thomas Serre

Evaluating the neurophysiological evidence for predictive processing as a model of perception

Kevin S. Walsh, David P. McGovern, Andy Clark, Redmond G. O'Connell

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Special Issue: The Year in Cognitive Neuroscience (vol 1464) - The New York Academy of Sciences

Newly-Discovered Gene Mutation Improves Cognitive Flexibility in Mice | Biology, Neuroscience – Sci-News.com

A team of U.S. researchers has discovered a genetic mutation that improves cognitive flexibility in mice.

Hu et al reveal a novel mechanism regulating reversal learning and provide potential targets for the treatment of neuropsychiatric disorders characterized by cognitive inflexibility. Image credit: Alexas Fotos.

Electrical signals stimulate chemical messengers that jump from neuron to neuron.

A gene called KCND2 codes for a protein that regulates potassium channels, which control electrical signals that travel along neurons.

Dr. Dax Hoffman from NIHs Eunice Kennedy Shriver National Institute of Child Health and Human Development and colleagues found that altering a single base pair in the KCND2 gene enhanced the ability of the protein to dampen nerve impulses.

Mice with this mutation performed better than mice without the mutation in a cognitive task.

The task involved finding and swimming to a slightly submerged platform that had been moved to a new location.

Mice with the mutation found the relocated platform much faster than their counterparts without the mutation.

The scientists now plan to investigate whether the mutation will affect neural networks in the animals brains.

Studying the gene and its protein may ultimately lead to insights on the nature of cognitive flexibility in people, they said.

It also may help improve understanding of epilepsy, schizophrenia, Fragile X syndrome, and autism spectrum disorder, which all have been associated with other mutations in KCND2.

The findings are published in the journal Nature Communications.

_____

J. Hu et al. 2020. Activity-dependent isomerization of Kv4.2 by Pin1 regulates cognitive flexibility. Nat Commun 11, 1567; doi: 10.1038/s41467-020-15390-x

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Newly-Discovered Gene Mutation Improves Cognitive Flexibility in Mice | Biology, Neuroscience - Sci-News.com

Tracking the Spread of Tau Through the Brain – Technology Networks

In the fight against neurodegenerative diseases such as frontotemporal dementia, Alzheimer's and Chronic Traumatic Encephalopathy, the tau protein is a major culprit. Found abundantly in our brain cells, tau is normally a team player it maintains structure and stability within neurons, and it helps with transport of nutrients from one part of the cell to another.All that changes when tau misfolds. It becomes sticky and insoluble, aggregating and forming neurofibrillary tangles within neurons, disrupting their function and ultimately killing them. Worse, it probably can take relatively few misfolded tau proteins from one cell to turn its neighbors into malfunctioning, dying brain cells.

"This abnormal form of tau starts to spread from cell to cell," said UC Santa Barbara neuroscientist Kenneth S. Kosik. "It's reminiscent of a serious problem that's known in biology, called prion diseases, such as mad cow disease."

Importantly, unlike true prion diseases, which are spread by contact with infected tissue or bodily fluid, prion-like diseases such as frontotemporal dementia and other tauopathies aren't contagious they can't be spread from person to person or by coming into contact with infected tissue. However, the replication is eerily familiar: A misfolded tau protein gets out of a cell and gets taken up by a normal neighboring cell. It then acts as a template in that cell, Kosik explained, which subsequently produces misfolded tau. Over and over again, the cells produce and secrete the toxic knockoff version of tau until whole regions of the brain are affected, which over time will rob a person of their cognitive and physical functions.

What if the spread could be contained? If caught early enough, controlling the proliferation of pathological tau could keep the neurodegenerative disease from progressing, and give the patient a shot at a normal life. But in order to do that, scientists first have to understand how the protein gets around.

Kosik and his team have uncovered one such mechanism by which tau travels from neuron to neuron. Not only does it shed light on the extensively studied but rather poorly understood tau propagation in neurodegenerative disease, it hints at a way to control the spread of pathological tau.

"The discovery of a mechanism by which tau transits from cell to cell provides a clue that will open up a deep structural approach to the design molecules that can prevent tau spread," said Kosik, who is the Harriman Professor of Neuroscience Research in UC Santa Barbara's Department of Molecular, Cellular, and Developmental Biology.

The major player in this mechanism of uptake and spread, it turns out, is the low-density lipoprotein called LRP1 (low density lipoprotein receptor-related protein 1). It's located on the brain cell membrane and is involved is several biological processes, among them helping the neuron take in cholesterol, which is used as part of cellular structure.

LRP1, the researchers discovered, takes up tau in neighboring cells after it escapes from a cell into the extracellular space. One of several low density lipoprotein receptors, LRP1 was singled out by process of elimination: By systematically inhibiting the expression of each of the members of this family via CRISPRi technology, and exposing them to tau, the researchers determined that genetic silencing of LRP1 effectively inhibited tau uptake.

"This protein is an interesting one in its own right because it's a little bit like an extracellular trash can," Kosik said. "It doesn't just pick up tau; if there's other rubbish out there, it also picks it up."

But what about tau is LRP1 recognizing? Digging deeper, the scientists found that a stretch of the amino acid lysine on the tau protein acts as kind of the secret handshake that opens the doors to the neuron.

"So these are all clues," Kosik said.Stopping the Spread"Since our cellular work showed that tau can interact with the cell-surface receptor LRP1 and that this causes tau's endocytosis, our hypothesis was that if we reduce LRP1 expression in the mice we should reduce the ability for neighboring neurons to take up tau," explained the study's lead author, postdoctoral researcher Jennifer Rauch.

To back their in-vitro studies, the researchers injected tau into mice, some of which had their LRP1 genes downregulated by a LRP1 suppressor RNA. The tau proteins were bound by a small string of amino acids to a green fluorescent protein to help the scientists observe tau after it was injected.

"As soon as this construct is in a cell, the amino acid connector gets cut, and the fluorescent protein and tau separate from each other," Kosik explained. What they found was that in the animals with normal LRP1, the tau had a tendency to spread; in the LRP1-suppressed mice, the protein stayed put, greatly reducing the likelihood that it would be taken up and replicated by other, normal neurons. "This is the first time we've seen the complete obliteration of tau spread," he said.

"When we reduce LRP1 expression, we see reduced tau spread in the animals," said Rauch, who has previously worked on the role of heparan sulphate proteoglycans on tau uptake. She pointed out a recent study that included Kosik and graduate student Juliana Acost-Uribe that described a patient with a severe genetic form of early-onset Alzheimers's but was spared getting the disease due to a second mutation that appeared to prevent tau spread. The team is keen to learn how this patient's second mutation might prevent tau spread possibly by interacting with LRP1.

"Next," Rauch said, "we are focusing on trying to decipher the interface of the tau-LRP1 interaction and understand if this could be a drug-able target."ReferenceRauch et al. (2020) LRP1 is a master regulator of tau uptake and spread. Nature. DOI: https://doi.org/10.1038/s41586-020-2156-5

This article has been republished from the following materials. Note: material may have been edited for length and content. For further information, please contact the cited source.

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Tracking the Spread of Tau Through the Brain - Technology Networks

Neuroscience Market Detailed Analysis of Current Industry Figures With Forecasts Growth by 2026| GE Healthcare, Siemens Healthineers, Noldus…

Complete study of the global Neuroscience market is carried out by the analysts in this report, taking into consideration key factors like drivers, challenges, recent trends, opportunities, advancements, and competitive landscape. This report offers a clear understanding of the present as well as future scenario of the global Neuroscience industry. Research techniques like PESTLE and Porters Five Forces analysis have been deployed by the researchers. They have also provided accurate data on Neuroscience production, capacity, price, cost, margin, and revenue to help the players gain a clear understanding into the overall existing and future market situation.

Key companies operating in the global Neuroscience market include _ GE Healthcare, Siemens Healthineers, Noldus Information Technology, Mightex Bioscience, Thomas RECORDING GmbH, Blackrock Microsystems, Tucker-Davis Technologies, Plexon, Phoenix Technology Group, NeuroNexus, Alpha Omega Neuroscience Breakdown Data by Type

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Segmental Analysis

The report has classified the global Neuroscience industry into segments including product type and application. Every segment is evaluated based on growth rate and share. Besides, the analysts have studied the potential regions that may prove rewarding for the Neuroscience manufcaturers in the coming years. The regional analysis includes reliable predictions on value and volume, thereby helping market players to gain deep insights into the overall Neuroscience industry.

Global Neuroscience Market Segment By Type:

, Whole Brain Imaging, Neuro-Microscopy, Electrophysiology Technologies, Neuro-Cellular Manipulation, Stereotaxic Surgeries, Animal Behavior, Other, Whole Brain Imaging, Neuro-Microscopy, and Electrophysiology Technologies are the top three types of neuroscience, with a combined market share of 62% Neuroscience Breakdown Data by Application,

Global Neuroscience Market Segment By Application:

Hospitals, Diagnostic Laboratories, Research Institutes, Other, Neuroscience is applied mostly in the hospital with a market share of 47%. It is followed by Research Institutes and Diagnostic Laboratories

Competitive Landscape

It is important for every market participant to be familiar with the competitive scenario in the global Neuroscience industry. In order to fulfil the requirements, the industry analysts have evaluated the strategic activities of the competitors to help the key players strengthen their foothold in the market and increase their competitiveness.

Key companies operating in the global Neuroscience market include _ GE Healthcare, Siemens Healthineers, Noldus Information Technology, Mightex Bioscience, Thomas RECORDING GmbH, Blackrock Microsystems, Tucker-Davis Technologies, Plexon, Phoenix Technology Group, NeuroNexus, Alpha Omega Neuroscience Breakdown Data by Type

Key questions answered in the report:

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TOC

Table of Contents 1 Report Overview1.1 Study Scope1.2 Key Market Segments1.3 Players Covered: Ranking by Neuroscience Revenue1.4 Market Analysis by Type1.4.1 Global Neuroscience Market Size Growth Rate by Type: 2020 VS 20261.4.2 Whole Brain Imaging1.4.3 Neuro-Microscopy1.4.4 Electrophysiology Technologies1.4.5 Neuro-Cellular Manipulation1.4.6 Stereotaxic Surgeries1.4.7 Animal Behavior1.4.8 Other1.5 Market by Application1.5.1 Global Neuroscience Market Share by Application: 2020 VS 20261.5.2 Hospitals1.5.3 Diagnostic Laboratories1.5.4 Research Institutes1.5.5 Other 1.6 Study Objectives 1.7 Years Considered 2 Global Growth Trends by Regions2.1 Neuroscience Market Perspective (2015-2026)2.2 Neuroscience Growth Trends by Regions2.2.1 Neuroscience Market Size by Regions: 2015 VS 2020 VS 20262.2.2 Neuroscience Historic Market Share by Regions (2015-2020)2.2.3 Neuroscience Forecasted Market Size by Regions (2021-2026) 2.3 Industry Trends and Growth Strategy 2.3.1 Market Top Trends 2.3.2 Market Drivers2.3.3 Market Challenges2.3.4 Porters Five Forces Analysis2.3.5 Neuroscience Market Growth Strategy2.3.6 Primary Interviews with Key Neuroscience Players (Opinion Leaders) 3 Competition Landscape by Key Players3.1 Global Top Neuroscience Players by Market Size3.1.1 Global Top Neuroscience Players by Revenue (2015-2020)3.1.2 Global Neuroscience Revenue Market Share by Players (2015-2020)3.1.3 Global Neuroscience Market Share by Company Type (Tier 1, Tier 2 and Tier 3)3.2 Global Neuroscience Market Concentration Ratio3.2.1 Global Neuroscience Market Concentration Ratio (CR5 and HHI)3.2.2 Global Top 10 and Top 5 Companies by Neuroscience Revenue in 20193.3 Neuroscience Key Players Head office and Area Served3.4 Key Players Neuroscience Product Solution and Service3.5 Date of Enter into Neuroscience Market3.6 Mergers & Acquisitions, Expansion Plans 4 Breakdown Data by Type (2015-2026)4.1 Global Neuroscience Historic Market Size by Type (2015-2020)4.2 Global Neuroscience Forecasted Market Size by Type (2021-2026) 5 Neuroscience Breakdown Data by Application (2015-2026)5.1 Global Neuroscience Market Size by Application (2015-2020)5.2 Global Neuroscience Forecasted Market Size by Application (2021-2026) 6 North America6.1 North America Neuroscience Market Size (2015-2020)6.2 Neuroscience Key Players in North America (2019-2020)6.3 North America Neuroscience Market Size by Type (2015-2020)6.4 North America Neuroscience Market Size by Application (2015-2020) 7 Europe7.1 Europe Neuroscience Market Size (2015-2020)7.2 Neuroscience Key Players in Europe (2019-2020)7.3 Europe Neuroscience Market Size by Type (2015-2020)7.4 Europe Neuroscience Market Size by Application (2015-2020)(2015-2020) (2015-2020) (2015-2020) (2015-2020) 8Key Players Profiles8.1 GE Healthcare8.1.1 GE Healthcare Company Details8.1.2 GE Healthcare Business Overview and Its Total Revenue8.1.3 GE Healthcare Neuroscience Introduction8.1.4 GE Healthcare Revenue in Neuroscience Business (2015-2020))8.1.5 GE Healthcare Recent Development8.2 Siemens Healthineers8.2.1 Siemens Healthineers Company Details8.2.2 Siemens Healthineers Business Overview and Its Total Revenue8.2.3 Siemens Healthineers Neuroscience Introduction8.2.4 Siemens Healthineers Revenue in Neuroscience Business (2015-2020)8.2.5 Siemens Healthineers Recent Development8.3 Noldus Information Technology8.3.1 Noldus Information Technology Company Details8.3.2 Noldus Information Technology Business Overview and Its Total Revenue8.3.3 Noldus Information Technology Neuroscience Introduction8.3.4 Noldus Information Technology Revenue in Neuroscience Business (2015-2020)8.3.5 Noldus Information Technology Recent Development8.4 Mightex Bioscience8.4.1 Mightex Bioscience Company Details8.4.2 Mightex Bioscience Business Overview and Its Total Revenue8.4.3 Mightex Bioscience Neuroscience Introduction8.4.4 Mightex Bioscience Revenue in Neuroscience Business (2015-2020)8.4.5 Mightex Bioscience Recent Development8.5 Thomas RECORDING GmbH8.5.1 Thomas RECORDING GmbH Company Details8.5.2 Thomas RECORDING GmbH Business Overview and Its Total Revenue8.5.3 Thomas RECORDING GmbH Neuroscience Introduction8.5.4 Thomas RECORDING GmbH Revenue in Neuroscience Business (2015-2020)8.5.5 Thomas RECORDING GmbH Recent Development8.6 Blackrock Microsystems8.6.1 Blackrock Microsystems Company Details8.6.2 Blackrock Microsystems Business Overview and Its Total Revenue8.6.3 Blackrock Microsystems Neuroscience Introduction8.6.4 Blackrock Microsystems Revenue in Neuroscience Business (2015-2020)8.6.5 Blackrock Microsystems Recent Development8.7 Tucker-Davis Technologies8.7.1 Tucker-Davis Technologies Company Details8.7.2 Tucker-Davis Technologies Business Overview and Its Total Revenue8.7.3 Tucker-Davis Technologies Neuroscience Introduction8.7.4 Tucker-Davis Technologies Revenue in Neuroscience Business (2015-2020)8.7.5 Tucker-Davis Technologies Recent Development8.8 Plexon8.8.1 Plexon Company Details8.8.2 Plexon Business Overview and Its Total Revenue8.8.3 Plexon Neuroscience Introduction8.8.4 Plexon Revenue in Neuroscience Business (2015-2020)8.8.5 Plexon Recent Development8.9 Phoenix Technology Group8.9.1 Phoenix Technology Group Company Details8.9.2 Phoenix Technology Group Business Overview and Its Total Revenue8.9.3 Phoenix Technology Group Neuroscience Introduction8.9.4 Phoenix Technology Group Revenue in Neuroscience Business (2015-2020)8.9.5 Phoenix Technology Group Recent Development8.10 NeuroNexus8.10.1 NeuroNexus Company Details8.10.2 NeuroNexus Business Overview and Its Total Revenue8.10.3 NeuroNexus Neuroscience Introduction8.10.4 NeuroNexus Revenue in Neuroscience Business (2015-2020)8.10.5 NeuroNexus Recent Development8.11 Alpha Omega10.11.1 Alpha Omega Company Details10.11.2 Alpha Omega Business Overview and Its Total Revenue10.11.3 Alpha Omega Neuroscience Introduction10.11.4 Alpha Omega Revenue in Neuroscience Business (2015-2020)10.11.5 Alpha Omega Recent Development 9Analysts Viewpoints/Conclusions 10Appendix10.1 Research Methodology10.1.1 Methodology/Research Approach10.1.2 Data Source10.2 Disclaimer10.3 Author Details

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Neuroscience Market Detailed Analysis of Current Industry Figures With Forecasts Growth by 2026| GE Healthcare, Siemens Healthineers, Noldus...

Woman With COVID-19 May Have Developed Rare Brain Disease From Coronavirus, Her Detroit Doctors Say – Newsweek

A woman in Detroit is thought to be the first person to have brain damage linked to COVID-19, according to the doctors who treated her. The clinicians stressed it is not clear if the rare condition was caused by the new coronavirus, but said it was important for doctors to be aware of it as a possible complication.

The case of the unidentified 58-year-old COVID-19 patient diagnosed with a rare form of brain damage known as acute necrotizing hemorrhagic encephalopathy was detailed in the journal Radiology. The condition has been linked with other viral infections in the past but not yet COVID-19, the authors said.

Dr. Elissa Fory, a neurologist at Detroit's Henry Ford health system who helped to diagnose the woman, said in a statement the patient had experienced a fever, cough and muscle aches. She was rushed by ambulance to an emergency room on March 19, after becoming confused, lethargic and disoriented.

According to the journal article, the woman tested positive for COVID-19, and negative for the flu. The team were unable to test the woman's cerebrospinal fluid for SARS-CoV-2, the virus that causes COVID-19 (not to be confused with the SARS virus).

MRI scans showed abnormal lesions in parts of the woman's brain associated with consciousness, sensation and memory function, the statement explained. "The 58-year-old female patient is hospitalized in serious condition," the health system said.

The authors of the paper explained acute necrotizing encephalopathy is a "rare complication" of viral infections such as the flu, particularly in children. It has been linked to cytokine storms, where the immune system dangerously overreacts. This can "result in blood-brain-barrier breakdown," they said.

Growing evidence suggests some COVID-19 patients might experience cytokine storms, according to the team.

Fory said: "This is significant for all providers to be aware of and looking out for in patients who present with an altered level of consciousness. We need to be thinking of how we're going to incorporate patients with severe neurological disease into our treatment paradigm.

"This complication is as devastating as severe lung disease."

As indicated in the map by Statista below, COVID-19 has spread to almost every country and territory in the world. According to Johns Hopkins University, almost 1 million cases have been confirmed worldwide, 47,522 people have died, and at least 195,929 have recovered. According to the CDC, common COVID-19 symptoms include a fever, cough, and shortness of breath.

Professor Neil Scolding of the U.K.'s University of Bristol Institute of Clinical Neurosciences, who did not work on the paper, told Newsweek: "This is the first reported case of severe brain inflammation related to COVID-19 and so is highly significant.

"We had suspected this kind of inflammation could occur, since it happensthough rarelywith conventional influenza virus infection, and with other viruses related to COVID-19."

Scolding said the study "serves as a valuable reminder to the medical community to look out for this complication."

Asked who might be most at risk of such a complication, Scolding said: "We don't know who will be most susceptible. With flu, it is children who are more likely to get this complicationbut children seem rather resistant to COVID-19, and the individual in this report is an adult."

Scolding stressed: "We do think it will remain a rather rare complication, and so I do not think people should start routinely looking out for confusion or other brain-related symptoms."

Professor Cris S. Constantinescu, of the Division of Clinical Neuroscience at the U.K.'s University of Nottingham Queen's Medical Centre, told Newsweek that while the case study describes a single report, it adds to the emerging evidence that SARS-cov-2 can affect the nervous system.

As the test to detect the virus in the cerebrospinal fluid could not be performed, "it is unclear whether the encephalitis was the direct effect of viral invasion" he said.

Constantinescu said it is "important" for people to look out for symptoms such as confusion as a potential COVID-19 symptom.

"In particular people with neurological diseases requiring immunosuppressive treatments such as multiple sclerosis or myasthenia gravis should be vigilant as they are at higher risk of infection, and have diminished immune responses to the infection.

"They should not always attribute new neurological symptoms [to] their underlying neurological disease. Also COVID-19 patients and carers should be aware of potential neurological problems," he said.

As the disease spreads, said Constantinescu, "we will become increasingly aware of neurological complications of COVID-19 and of the implications of COVD-19 infections in people with underlying neurological conditions. Even rare complications such as this one have great informative value."

Hygiene advice

Medical advice

Mask and glove usage

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Woman With COVID-19 May Have Developed Rare Brain Disease From Coronavirus, Her Detroit Doctors Say - Newsweek

Lilly and Sitryx Announce Licensing and Research Collaboration to Discover and Develop New Immunometabolic Medicines – PharmiWeb.com

INDIANAPOLISandOXFORD, England,March 31, 2020/PRNewswire/ --Eli Lilly and Company(NYSE: LLY) today announced an exclusive global licensing and research collaboration with Sitryx, a biopharmaceutical company focused on regulating cell metabolism to develop disease-modifying therapeutics in immuno-oncology and immuno-inflammation. The collaboration will study up to four novel preclinical targets identified by Sitryx that could lead to potential new medicines for autoimmune diseases.

"AsLillyseeks to develop new and unique medicines for people suffering with autoimmune diseases, we are actively exploring a variety of scientific approaches both in our own labs and with external partners," saidAjay Nirula, M.D., Ph.D., vice president of immunology atLilly. "Regulating the metabolism of immune cells is a promising approach to treating these diseases, and we look forward to working with the talented researchers at Sitryx to advance their novel immunometabolism targets."

"We are excited to partner withLilly, one of the global leaders in the field of immunology, to pursue the discovery of novel targets and the development of innovative therapies for autoimmune and inflammatory diseases in the fast-emerging area of immunometabolism," saidNeil Weir, Ph.D.,chief executive officer of Sitryx. "This agreement is transformational for Sitryx and further validates the strength of our scientific expertise and that of our Founder network and the potential for Sitryx to become a leader in this field."

Under the terms of the agreement, Sitryx will receive an upfront payment of$50 millionandLillywill make a$10 millionequity investment in Sitryx. Sitryx will be eligible to receive potential development milestones up to$820 million, as well as commercialization milestones and royalty payments on potential sales in the mid- to high-single digit range. In return, Sitryx will grantLillyan exclusive, worldwide license to develop and commercialize up to four novel immunometabolism targeted therapeutics, including Sitryx's two lead projects.Lillyand Sitryx will establish a 5-year research collaboration to support the development of the therapeutics, with Sitryx responsible for drug discovery, whileLillywill fund and manage the clinical development and commercial phase of the collaboration.

This transaction is subject to customary closing conditions. The transaction will be reflected inLilly's reported results and financial guidance according to Generally Accepted Accounting Principles (GAAP). There will be no change toLilly's 2020 non-GAAP earnings per share guidance as a result of this transaction.

About SitryxSitryx is a biopharmaceutical company focused on regulating cell metabolism to develop disease-modifying therapeutics in immuno-oncology and immuno-inflammation. Sitryx's proprietary science is led by a highly experienced management team and supported by world class academic founders. Sitryx was founded by six world-leading researchers in the field of immunology and metabolism;Houman Ashrafian,Luke O'Neill,Jonathan Powell,Jeff Rathmell,Michael RosenblumandPaul Peter Tak. Together they have published more than 1,000 papers in the field, making multiple key breakthroughs in our understanding of how critical energetic status is to the behavior of immune cells and in the broader field of immunology. In 2018, Sitryx raised$30 millionSeries A funding from an international syndicate of specialist investors includingSV Health Investors,Sofinnova Partners,Longwood Fundand GSK. The company has a pipeline of projects at multiple stages of drug discovery. Sitryx is headquartered inOxford, UK. For more information, please visitwww.sitryx.com.

AboutEliLillyand CompanyLillyis a global healthcare leader that unites caring with discovery to create medicines that make life better for people around the world. We were founded more than a century ago by a man committed to creating high-quality medicines that meet real needs, and today we remain true to that mission in all our work. Across the globe,Lillyemployees work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to communities through philanthropy and volunteerism. To learn more aboutLilly, please visit us atwww.lilly.com. C-LLY

LillyForward-Looking StatementThis press release contains forward-looking statements (as that term is defined in the Private Securities Litigation Reform Act of 1995) about the benefits of a collaboration betweenLillyand Sitryx, and reflectsLilly's current beliefs. However, as with any such undertaking, there are substantial risks and uncertainties in the process of drug development and commercialization. Among other things, there can be no guarantee thatLillywill realize the expected benefits of the collaboration, or that the collaboration will yield commercially successful products. For a further discussion of these and other risks and uncertainties that could cause actual results to differ fromLilly's expectations, please seeLilly's most recent Forms 10-K and 10-Q filed with theU.S. Securities and Exchange Commission.Lillyundertakes no duty to update forward-looking statements.

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Lilly and Sitryx Announce Licensing and Research Collaboration to Discover and Develop New Immunometabolic Medicines - PharmiWeb.com

Heat Biologics Announces Formation of COVID-19 Advisory Board – Yahoo Finance

DURHAM, NC / ACCESSWIRE / April 1, 2020 / Heat Biologics, Inc. ("Heat") (HTBX), a clinical-stage biopharmaceutical company specialized in the development of novel therapeutic and prophylactic vaccines, including one for coronavirus COVID-19, announced today the formation of its COVID-19 Advisory Board (CAB) with four key appointments: Justin Stebbing MD, PhD, Raymond Pickles, PhD, Natasa Strbo MD, DSc, and Lanying Du, PhD.

Heat's COVID-19 Advisory Board was established with leading thought leaders to propel Heat's COVID-19 vaccine and COVID-19 diagnostic programs. The combined Advisory Board has expertise in areas of coronavirus and related respiratory virus biology and infection, immunotherapy, and vaccines. Heat recently announced a research collaboration with the University of Miami Miller School of Medicine to develop a vaccine leveraging Heat's proprietary gp96 platform designed to target the SARS-CoV-2 coronavirus that causes COVID-19. Under a separate collaboration with the University of Miami Miller School of Medicine, Heat also intends to develop a proprietary COVID-19 point-of-care diagnostic test.

The CAB members include:

Jeff Wolf, Chief Executive Officer of Heat Biologics, commented, "We are thrilled to have attracted leading experts in immunotherapy and vaccines to support Heat as we continue to develop Heat's COVID-19 vaccine and COVID-19 diagnostic programs. We look forward to working closely with the CAB to advance our programs to help combat the current COVID-19 pandemic."

Justin Stebbing MD, PhD, is a Professor of Cancer Medicine and Oncology, Consultant Oncologist, at the Imperial College and Imperial College Healthcare NHS Trust. Professor Justin Stebbing specializes in a range of malignancies, their treatment with immunotherapy (breast, GI and lung and clinical trials), having originally trained in medicine at Trinity College Oxford, where he gained a first-class degree. After completion of junior doctor posts in Oxford, he undertook training and a residency program at The Johns Hopkins Hospital in the US, returning to London to continue his career in oncology at The Royal Marsden and then St Bartholomew's Hospitals. Professor Stebbing's original PhD research investigated the interplay between the immune system and cancer; he was appointed a senior lecturer in 2007, and a Professor in 2009. Professor Stebbing has published over 600 peer-reviewed papers in journals such as the Lancet, New England Journal, Blood, the Journal of Clinical Oncology, Annals of Internal Medicine, as well as writing regularly for national newspapers and presenting new data on optimal cancer therapies at the major international conferences.

Raymond Pickles, PhD, is an associate professor in the Department of Microbiology and Immunology within the UNC School of Medicine. His research is focused on how viruses infect the respiratory tract of humans and other animal species and why highly pathogenic viruses often result in more severe airway disease. He has 30 years of experience working with models of the respiratory tract and has used these models to understand infection outcomes with Respiratory Syncytial Virus (RSV), Adenoviruses, newly emerging avian influenza viruses, and newly emerging coronaviruses including SARS. He received his PhD from the University of Cambridge before completing Post-Doctoral Studies in the Division of Pulmonary Medicine at UNC-Chapel Hill

Natasa Strbo MD, DSc, is an assistant professor of microbiology and immunology at the University of Miami, Miller School of Medicine. Dr. Strbo is also a co-developer of Heat's gp96 platform and has spent many years advancing the platform as a vaccine against HIV and malaria. Dr. Strbo's current research is focused on devising a novel strategy for achieving as complete a protection as possible, the ultimate goal being the future development of an efficacious heat shock protein (HSP) gp96-Ig vaccine against HIV, malaria, ZIKA, CMV, COVID-19 and other emerging infectious diseases. Dr. Strbo was the recipient of a Miami CTSI KL2 Award (2013-2016) to study vaccine-induced immune responses in the reproductive tract of HIV-infected humanized mice and she was also awarded the University of Miami Glaser Award for 2016 to further develop HIV vaccine technology.

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Lanying Du, PhD, is a Member at the New York Blood Center (NYBC) and is the Head of Viral Immunology Laboratory at the Lindsley F. Kimball Research Institute of NYBC. Dr. Du's research focuses on the development of effective and safe vaccines and therapeutic agents to prevent and treat emerging and reemerging infectious diseases caused by coronaviruses, including severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), also known as 2019 novel coronavirus (2019-nCoV), Middle East respiratory syndrome coronavirus (MERS-CoV), SARS-CoV, and other coronaviruses with pandemic potential, influenza viruses, as well as flaviviruses, including Zika virus and dengue virus. Dr. Du's research also focuses on the study of pathogenic mechanisms of these viruses, based on which to design novel vaccines and therapeutic antibodies. Her research tools include rational design of novel vaccines and therapeutics, mRNA technology, drug screening, antibody production and evaluation.

About Heat Biologics, Inc.

Heat Biologics is a biopharmaceutical company developing immunotherapies designed to activate a patient's immune system against cancer and other diseases using its proprietary gp96 platform to activate CD8+ "Killer" T-cells. Heat has completed enrollment in its Phase 2 clinical trial for advanced non-small cell lung cancer with its gp96-based HS-110 therapeutic vaccine. HS-110 is the company's first biologic product candidate in a series of proprietary immunotherapies designed to stimulate a patient's own T-cells. Heat Biologics has also launched a program in collaboration with the University of Miami to develop a vaccine designed to protect against the COVID-19 Coronavirus. Heat has numerous other pre-clinical programs at various stages of development. For more information, please visit http://www.heatbio.com.

Forward-Looking Statement

This press release includes forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995 on our current expectations and projections about future events. In some cases, forward-looking statements can be identified by terminology such as "may," "should," "potential," "continue," "expects," "anticipates," "intends," "plans," "believes," "estimates," and similar expressions. These statements are based upon current beliefs, expectations, and assumptions and include statements such as the support to be received by the SAB members with respect to Heat's continued development of its COVID-19 vaccine and COVID-19 diagnostic programs and advancing Heat's programs to help combat the current COVID-19 pandemic. These statements are subject to a number of risks and uncertainties, many of which are difficult to predict, including the contribution of the SAB, the ability of Heat together with researchers at the University of Miami to develop a proprietary COVID-19 point-of-care diagnostic test, the ability of Heat's vaccine platform to provide protection against COVID-19, the ability of Heat's therapies to perform as designed, to demonstrate safety and efficacy, as well as results that are consistent with prior results, the ability to enroll patients and complete the clinical trials on time and achieve desired results and benefits, Heat's ability to obtain regulatory approvals for commercialization of product candidates or to comply with ongoing regulatory requirements, regulatory limitations relating to Heat's ability to promote or commercialize its product candidates for specific indications, acceptance of its product candidates in the marketplace and the successful development, marketing or sale of products, Heat's ability to maintain its license agreements, the continued maintenance and growth of its patent estate, its ability to establish and maintain collaborations, its ability to obtain or maintain the capital or grants necessary to fund its research and development activities, its ability to continue to maintain its listing on the Nasdaq Capital Market and its ability to retain its key scientists or management personnel, and the other factors described in Heat's most recent annual report on Form 10-K for the year ended December 31, 2018 filed with the SEC, and other subsequent filings with the SEC. The information in this release is provided only as of the date of this release, and Heat undertakes no obligation to update any forward-looking statements contained in this release based on new information, future events, or otherwise, except as required by law.

CONTACT:

David Waldman+1 919 289 4017investorrelations@heatbio.com

SOURCE: Heat Biologics Inc.

View source version on accesswire.com: https://www.accesswire.com/583405/Heat-Biologics-Announces-Formation-of-COVID-19-Advisory-Board

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Heat Biologics Announces Formation of COVID-19 Advisory Board - Yahoo Finance

REPEAT – QUESTCAP TO INVEST $1 MILLION WITH SUNNYBROOK RESEARCH INSTITUTE TO ESTABLISH THE SUNNYBROOK TRANSLATIONAL RESEARCH GROUP FOR EMERGING AND…

TORONTO, April 02, 2020 (GLOBE NEWSWIRE) --

QuestCap Inc. (QuestCap or the Company) (CSE: QSC; OTCMKTS: COPRF; FRA: 34C1) is pleased to announce an investment of $1 million in the Sunnybrook Research Institutes COVID-19 research. With these funds, Sunnybrook will establish the Sunnybrook Translational Research Group for Emerging and Respiratory Viruses (SERV) and QuestCap will receive a 3.5% royalty on any revenues earned by Sunnybrook from the commercialization of any of the research done by SERV.

Led by infectious diseases physician and microbiologist Dr. Samira Mubareka, SERVs work will focus on three crucial streams of research: vaccines and therapeutics, virus biology and transmission prevention. Dedicated investment in SERV means Dr. Mubareka and her team will be able to accelerate the pace of further research into COVID-19 at a crucial time.

Dr. Lawrence Steinman and Mike McCarthy Appointed as Advisors

QuestCap is pleased to announce the appointment of Dr. Lawrence Steinman and Mike McCarthy to the board of advisors. Dr. Lawrence Steinman is Professor of Neurology, Neurological Sciences and Pediatrics at Stanford University and Chair of the Stanford Program in Immunology from 2001 to 2011.

Mike McCarthy has more than 14 years of experience with the Ontario Ministry of Health and Long-Term Care and 24 years in health policy and delivery. He was appointed Senior Policy Advisor to the Progressive Conservative Minister of Health of Ontario, advising on physician, nursing and primary care, public health, laboratories, OHIP, organ transplant, HIV and blood issues. In 2003, he provided strategic support and counsel to the government of Ontario during the SARS outbreak.

Lawrence Steinman stated that, The Sunnybrook technology will be a key tool for the development of both powerful and safe vaccines against COVID-19, and for the development of point of care and even home diagnostics to test whether one is immune to the COVID-19 virus. Those who are immune can return to work and can provide safe and needed duties to the community. It would be especially important to know if you are a health care worker, grocer or delivery person whether or not you have immunity. You could then be safe and carry on as a SuperWomen or SuperMan in these times, knowing you are immune! Mike McCarthy adds I look forward to advising QuestCap in its visionary efforts to bring innovative testing and vaccine technologies to Canada and the world to combat COVID-19.

The Company has granted 500,000 stock options to Mr. Steinman pursuant to the Companys stock option plan. The stock options shall vest in four equal instalments every three months such that all stock options fully vest by the date that falls 12 months from the date of grant and may be exercised at a price of $0.305 per common share for a period of five years from the date of grant. This grant of options is subject to the approval of the Canadian Securities Exchange.

Sunnybrook Translational Research Group

Sunnybrook has been at the global forefront of the COVID-19 pandemic since the first Canadian case was identified, both clinically and on the research front. Dr. Mubareka, along with clinical microbiologist Dr. Robert Kozak and a team of close collaborators, has led Sunnybrooks research response efforts since the earliest days of the pandemic. Their work has been globally significant, leading to early implementation of a hospital-based COVID-19 test. Most crucially, on March 10, 2020, their team isolated the agent responsible for the ongoing outbreak of COVID-19. The isolated virus is helping researchers in Canada and elsewhere to develop better diagnostic testing, treatments and vaccines, and gain a better understanding of the viruss biology, evolution and clinical shedding.

This is extremely time-sensitive research, says Dr. Mubareka. As a scientist on the frontlines, I have seen the devastation this virus can cause. We all feel the effects of physical distancing as our lives are fundamentally changed. This is why support from our community is so important right now. The more we understand how this virus behaves, the better we can limit its spread as we race to find a treatment or vaccine. This investment will be put to work immediately toward our human and operational funding needs to rapidly accelerate research into COVID-19.

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Now is the time to dedicate as many resources as possible to stopping the spread of this highly contagious virus, explains Dr. Andy Smith, Sunnybrooks President and CEO. On behalf of Sunnybrook, I would like to extend my deepest thanks to QuestCap for stepping up with this inspiring investment. Your support will have a direct impact on the lives of countless people in our communities, across Canada and around the world.

With these crucial tools in hand, QuestCap saw an opportunity to give this research a major boost at a critical juncture. As countries grapple with the effects of COVID-19, there has been a collective global effort to help minimize the impacts of this deadly virus, says Stan Bharti, Co-Chairman of QuestCap. QuestCap, through its investment platform, is looking to do its part by providing a critical investment to help fund the vital research being conducted by Dr. Mubareka, Dr. Kozak and their teams.

The investment to Sunnybrook will help researchers in Canada and across the world develop better diagnostic testing, treatments and vaccines, and gain a better understanding of SARS-CoV-2 biology, evolution and clinical shedding for the development of commercial applications (Commercial Applications). As consideration for its investment, QuestCap will receive a 3.5% royalty on any revenue earned by Sunnybrook from the any Commercial Applications resulting from the research conducted by SERV.

At a time of global uncertainty as COVID-19 continues to devastate people, families and entire countries, the urgency of research has never been greater, says Dr. Kullervo Hynynen, Vice President of Research & Innovation at Sunnybrook. Yet, often times, there simply isnt enough funding for research. I am deeply grateful to QuestCap for this clear statement on supporting the power of research to save and change lives.

About the Research

SERV is a three-pronged COVID-19 research response program, consisting of the following critically important areas of focus:

1. Virus biology (genomics): Identifying the genetic sequence of a virus is an essential step for identifying key targets for treatments and vaccines. It also tells the story of origin and its relation to other viruses. This approach provides precision genomic data, which will be essential for outbreak investigation. Funds for SERV allow Sunnybrook scientists to turn around whole genome viral sequences at the site of care: Sunnybrook.

2. Vaccines and therapeutics: Our ability to identify and isolate the virus that causes COVID-19, based on samples from infected patients, allows us to collaborate on antiviral research and conduct our own vaccine and transmission work. With SERV, Sunnybrook will share our findings about the virus within the Canadian research and diagnostic community, thereby driving further innovative solutions to the COVID-19 pandemic.

3. Transmission prevention: As part of a World Health Organizations effort to evaluate risk to health-care workers of providing certain support measures, such as high-flow oxygen use, Sunnybrook is building a simulation space for live virus experiments using mannequins with funds for SERV. This is important because protecting care providers is key to preventing the spread of the virus within hospitals.

About Lawrence Steinman

Steinman is Professor of Neurology, Neurological Sciences and Pediatrics at Stanford University and Chair of the Stanford Program in Immunology from 2001 to 2011. His research focuses on antigen specific tolerance in autoimmune disease and in gene therapy for degenerative neurologic diseases. He has elucidated what provokes relapses and remissions in multiple sclerosis (MS). He is taking forward a pivotal clinical trial with antigen specific tolerization therapy for type 1 diabetes. He serves as attending neurologist at Stanfords Lucille Packard Childrens Hospital. Steinman is an elected member of the US National Academy of Sciences and the National Academy of Medicine.

Steinman was senior author on the 1992 Nature article that led to the drug Tysabri, approved for MS and Crohns disease. Tysabri has been taken by over 200,000 individuals with MS.

Dr. Steinman graduated from Dartmouth College, Magna Cum Laude in Physics. His MD is from Harvard Medical School. He was a post-doctoral fellow in chemical immunology fellow at the Weizmann Institute of Science. After neurology residency he remained on the faculty in 1980. He has received numerous honors, including the John M. Dystel Prize in 2004, the Javits Neuroscience Investigator Award from the NINDS twice, the Charcot Prize in MS research, and the Cerami Prize in Translational Medicine. Steinman is a member of both the National Academy of Sciences, and the National Academy of Medicine.

Dr. Steinman co-founded several biotech companies, including Neurocrine, Atreca, 180 Therapeutics, and Tolerion. He was a Director of Centocor from 1988 until its sale to Johnson and Johnson.

About Mike McCarthy

Mike is widely recognized across Canada as a stellar health care advocate and system expert. As a volunteer Vice-President of the Canadian Hemophilia Society, Mike was the national spokesperson for Canadians infected by blood tainted with Hepatitis C. His tireless efforts resulted in a landmark $2 billion settlement with the federal government in 2006, and the Queens Golden Jubilee Award presented by the Governor General of Canada.

Presently Mike is a Principal at Grosso McCarthy and provides counsel to clients in both the not-for-profit and for-profit sectors. He helps clients navigate provincial, federal and international governments at the levels of the civil service and elected officials. Mike has also been on the front lines of health care, working for 18 years as a psychiatric nurse.

As a principal with Grosso McCarthy, Mike builds on more than 14 years of experience with the Ontario Ministry of Health and Long-Term Care and 24 years in health policy and delivery. He was appointed Senior Policy Advisor to the Progressive Conservative Minister of Health of Ontario, advising on physician, nursing and primary care, public health, laboratories, OHIP, organ transplant, HIV and blood issues.

In 2003, he provided strategic support and counsel to the government of Ontario during the SARS outbreak.

About QuestCap

QuestCap is an investment company that seeks to enhance shareholder value over the long term by opportunistically making various investments that may include, without limitation, the acquisition of equity, debt or other securities of publicly traded or private companies or other entities, financing in exchange for pre-determined royalties or distributions and the acquisition of all or part of one or more businesses, portfolios or other assets.

For additional information, please contact:

G Scott Moore

Co-Chairmansmoore@forbesmanhattan.com1-416-861-5903

Media contact:

Wynn TheriaultThirty Dash Communications34 King St East #400Toronto M5C 2X8416.710.3370

Cautionary Note Regarding Forward-lookingInformation

This press release contains "forward-looking information" within the meaning of applicable Canadian securities legislation. Forward-looking information includes, but is not limited to, statements with respect to the investment with SERV; the grant of options; and Sunnybrook and the appointment of advisory board members. Generally, forward-looking information can be identified by the use of forward-looking terminology such as "plans", "expects" or "does not expect", "is expected", "budget", "scheduled", "estimates", "forecasts", "intends", "anticipates" or "does not anticipate", or "believes", or variations of such words and phrases or state that certain actions, events or results "may", "could", "would", "might" or "will be taken", "occur" or "be achieved". Forward-looking information is subject to known and unknown risks, uncertainties and other factors that may cause the actual results, level of activity, performance or achievements of the Company, as the case may be, to be materially different from those expressed or implied by such forward-looking information. Although the Company has attempted to identify important factors that could cause actual results to differ materially from those contained in forward-looking information, there may be other factors that cause results not to be as anticipated, estimated or intended. There can be no assurance that such information will prove to be accurate, as actual results and future events could differ materially from those anticipated in such statements. Accordingly, readers should not place undue reliance on forward-looking information. The Company does not undertake to update any forward-looking information, except in accordance with applicable securities laws.

NEITHER THE CANADIAN SECURITIES EXCHANGE NOR ITS REGULATION SERVICES PROVIDER HAS REVIEWED OR ACCEPTS RESPONSIBILITY FOR THE ADEQUACY OR ACCURACY OF THIS RELEASE.

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REPEAT - QUESTCAP TO INVEST $1 MILLION WITH SUNNYBROOK RESEARCH INSTITUTE TO ESTABLISH THE SUNNYBROOK TRANSLATIONAL RESEARCH GROUP FOR EMERGING AND...

The first US coronavirus patients are being treated with convalescent plasma therapy. Will it work? Not even the doctors know – USA TODAY

Why a treatment used for over a century on diseases like measles, mumps and influenza could work to treat the new coronavirus strain. USA TODAY

In New York and Houston, pints of straw-colored convalescent plasma have dripped into the veinsof fiveU.S. coronavirus patients.Hundreds more there and across the nation are set to follow.

Whether the plasma, derived from the blood of people who recovered from COVID-19, will help them fight off the devastating disease caused by the new coronavirus that haskilled more than 5,100Americans is unknown. In less than three weeks, the effort to find out has gone from an ideato a worldwide program entirely self-organized by medical researchers.

Like so muchabout the desperate efforts to fight the COVID-19 pandemic, its seat-of-the-pants medicine. Doctors dont know whether it will work buthopeto find out in weeks, not the years it typically takes for studies to yield answers.

Our treatments began on Saturday, said AniaWajnberg, an internist at Mount Sinai Medical Center in New York City who directs its Serum Antibody program.

There are 8 strains of the coronavirus circling the globe: Here's what clues theygive scientists.

It was only four days before that, March 24, that the U.S. Food and Drug Administration began allowing researchers to request emergency authorization to test whether the plasma will help.

Plasma is the almost clear liquid that remains after red and white blood cells and platelets are removed from blood. It contains antibodies that can fight disease.

The Chinese paper came out days ago, but days are feeling like years to me right now, Wajnberg said, referring to a paper published March 27 in the Journal of the American Medical Associationthat described a test of convalescent plasma on five critically ill patients in Shenzhen, China.

For Wajnberg and thousands of other doctors worldwide, nothing feels fast enough.

One of the first COVID-19 antibody tests in the USA is being used on recovered patients in New York City to determine whether they produced a high amount of antibodies. If so, they could donate their antibody-rich plasma to help others mount an immune response.(Photo: Icahn School of Medicine at Mount Sinai)

Methodist Hospital in Houston began recruiting plasma donors Friday and gave the first plasmatransfusions to a COVID-19 patient the following day.

Its a gamble of time, energy and money, said William Schaffner, a professor of preventive medicine and infectious disease at Vanderbilt University School of Medicine in Nashville, Tennessee.

Convalescent plasma therapy has a mixed history of success. It's time-consuming, expensive and difficult to deploy on a large scale. Even so,hes all in favor of it.

Any port in a storm and weve got one heck of a storm out there, he said.

The project, dubbed the National COVID-19 Convalescent Plasma Project, posted a protocol for clinical trials on its website.

"The world is downloading it," said Arturo Casadevall, one of the project's organizers and chairman of molecular microbiology and immunology at Johns Hopkins Bloomberg School of Public Health.

The plasma iscollected from patients who recovered from COVID-19. Each donates apintof blood. The red and white blood cells are separated and put back intothe donors bloodstream while the blood plasma, rich with virus-fighting antibodies, is kept aside.

Those coronavirus 'cures' you're hearing about?They're fake.

The donor and the patient must be fromcompatibleblood types, and the plasma is tested for multiple diseases, including COVID-19, HIV and hepatitis, to ensure it cant transfer them.

Though convalescent plasma (from the blood of people convalescing, or recovered, from a disease) has been used successfully in outbreaks of other diseases, such as polio, measles and mumps, its by no means a slam-dunk.

Its been used for other viruses, some with efficacy and some without, Wajnberg said.

The plasma showed promising results in the small Chinese studyposted as a preprint March 27. Another preprint, released March 16, about plasma treatment in10 severely ill patients in Wuhan, China, found similar results.

Blood plasma is processed at the New York Blood Center. Blood plasma contains antibodies that can fight diseases. An experimental treatment is being tried to use blood plasma from people who recovered from COVID-19 to treat patients who are severely ill with the disease.(Photo: New York Blood Center)

Preprints are papers posted to online open-access sites before theyhave gone through the rigorous scientific peer review process, soinformation can be shared rapidly. During the COVID-19 crisis, they have been crucial in quickly disseminating essential data.

In bothstudies, almost all the patients also receivedantiviral and other treatments, making it difficult to know in a group of only 15 patients what specifically helped.

For now, plasma therapy isone of few options for doctors when critically ill patients "don't have much time,"saidEric Salazar, principal investigator in the Department of Pathology and Genomic Medicine at the Houston Methodist Hospital and Research Institute.

Have you recovered from coronavirus?Here's how you can help doctors find a treatment.

Convalescent serum therapy could be a vital treatment route because, unfortunately, there is relatively little to offer many patients except supportive care, Salazar said.

No one anticipates the treatment will have a "Lazarus-like effect on the really ill," cautioned Michael Joyner, who worked to set up trials at the Mayo Clinic in Rochester, Minnesota, where he is a professor of anesthesiology.

"What's more likely is that the slope of the patient's decline will gradually slow and that they can be weaned off of ventilation," he said.

The idea of giving desperately ill patients blood plasma from people who recovered from the same illness is more than a century old and was first used to treat a German child suffering from diphtheria.

Using it to fight COVID-19 has gone fromone paper published in the Journal of Clinical Investigation on March 13 suggesting the idea of a large trial to a broad program in less than three weeks.

Its become an international effort, showing the ability of scientists to self-organize at a speed unimaginableeven three months ago. As of Monday, more than 100 researchers and 40 large hospitals in 20 states are involved in the effort to bring survivor plasma to clinical trials, according to project leaders.

'Who lives and who dies': In worst-case coronavirus scenario, ethics guide choices on who gets care

Other countries are joining what began as a grassroots endeavor by doctors and scientists.

"We brought in the United Kingdom over the weekend. Ireland, too," said Casadevall, who co-wrote the paper March 13.

When a person is infected with COVID-19, the body creates blood proteins called antibodies to attack the virus, said Mark Slifka, a viral immunologist at the Oregon Health and Science University in Portland.

When the body mounts an antibody response, it clears the virus, and then you maintain that antibody response, said Slifka, who studies the bodys immunological memory after vaccination or infection.

Depending on the disease, the body keeps making those antibodies for weeks to months to a lifetime. No one knows how long the antibodies against COVID-19 will stay in the bloodstream, but work on similar coronaviruses suggestsits at least a year, he said.

The plasma is taken from people who were exposed to or contracted COVID-19 about three weeks ago and recovered. That seems to be the time the body requires to mount a strong immune response to the virus.

People who tested positive for COVID-19 and fully recovered can register on the Plasma Project's website to see whether they are eligible and if there's a plasma donation program near them.

Almost all of the people who learned they are positive for antibodies to the virus and eligible to donate plasmahave offered to do so.

The race for a vaccine: Thousands of scientists are studying 41 possibilities

Thats been a bright spot in all this, everybody wants to help. Its nice to see, Wajnberg said.

Patients are given one to two units of the plasma, about one to two pints. Doctors hope to find out quickly how much is required.

At Mount Sinai, a committee is deciding the right candidates forpossible treatment. Only hospitalized patients with severe clinical disease are considered. Those who get the plasma are meticulously tracked to see its impact.

If it does help, scientists hope to build a pool of plasma for all blood types that can be given to severely ill patients.

Maybe in a few weeks, well be able to report our first 10 or 20 patients, Wajnberg said.

One donors blood is enough to give to no more than one or two recipients. We will need a lot of donors, Wajnberg said.

The Plasma Project is working on the problem, and"a national distribution plan (for the plasma) is being worked on as we speak," Joyner said.

Your coronavirus questions, answered: Are malaria meds working? How many people have recovered?

The effort is an example of how medical researchers are self-organizing in the face of the COVID-19 pandemic.The project has proceeded with "terrific" help from the FDA, Casadevall said, but has no government lead.

"What hasn't materialized is a federal coordinator," Casadevall said.

The effort is guided by an executive committee from theIcahn School of Medicine at Mount Sinai, the Mayo Clinic School of Medicine, Washington University School of Medicine in St. Louis, Michigan State University and Johns Hopkins University. The groupconvenes meetings by conference call once or twice a week.

The project's unofficial motto reflects the doctors'drive to do everything they can to fight the virus:"Don't permit what you cannot do to interfere with what you can do."

Weise of USA TODAY reported from San Francisco;Johnson of the Journal Sentinel, part of the USA TODAY Network, reported from Milwaukee.

Read or Share this story: https://www.usatoday.com/story/news/health/2020/04/01/coronavirus-plasma-therapy-5-us-patients-covid-19-donors/5090946002/

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The first US coronavirus patients are being treated with convalescent plasma therapy. Will it work? Not even the doctors know - USA TODAY

Carterra to Provide Antibody Screening and Characterization for the Coronavirus Immunotherapy Consortium (CoVIC) – Technology Networks

Carterra Inc., specialists in high-throughput antibody screening and characterization tools, and La Jolla Institute for Immunology (LJI) have announced that they will use Carterras proprietary LSA platform to screen hundreds of antibodies in just a few days, allowing CoVIC to move therapeutic candidates to the clinic as early as this summer.

La Jolla Institute for Immunology (LJI) has been awarded a $1.73 million grant by the Bill & Melinda Gates Foundation to establish a Coronavirus Immunotherapy Consortium (CoVIC) as part of the foundations global efforts to stem the tide of the current coronavirus outbreak, the Institute announced yesterday. Antibody therapies are often the first novel therapies advanced for an emerging infectious disease.

Headquartered at LJI, CoVIC will serve as a clearinghouse to understand which antibodies are most effective against the novel coronavirus SARS-CoV-2 and to accelerate the research pipeline to provide immunotherapeutics in order to protect vulnerable individuals from severe manifestations of COVID-19 in all parts of the world, including low-resource settings.

This effort is being funded as part of the COVID-19 Therapeutics Accelerator launched in early March by the Gates Foundation, Wellcome, and Mastercard. The Accelerator provides fast and flexible funding at key stages of the development process to de-risk the pathway for drugs and biologics to prevent and treat COVID-19.

The effort is led by Erica Ollmann Saphire, Ph.D., a professor in LJIs Center for Infectious Disease and Vaccine Research, who draws on her broad research experience guiding the development of antibody drugs and galvanizing a global research coalition that helped define which therapeutic antibodies effectively combat disease in humans infected with Ebola virus.

We are thrilled that Carterra will provide full antibody characterization data using affinity measurements and, potentially more importantly, ultra-high resolution information of the epitopes, says Dr. Ollmann Saphire. Knowing how well these antibodies bind to the target is important but understanding their mechanism of action and how different antibodies can complement each other will determine what ends up in the clinic.

Traditional antibody discovery requires a primary screen of ever-expanding antibody libraries. Only a small group of candidate antibodies are then characterized on traditional, low-throughput, low-resolution biosensor tools which provide real-time readout of the binding profile. This workflow runs the risk that potential drug candidates could be missed or that the process of candidate selection could be exceedingly long.

Carterras LSA is turning that model on its head by enabling the high-resolution analysis of entire libraries, combining screening and characterization into one seamless step, thereby minimizing the risk of missing a potent therapeutic candidate. The LSAs dramatic throughput condenses months of work into days. Infectious diseases are ideal for leveraging the power of the LSA platform as evidenced in recent studies of Yellow Fever and Ebola where the LSA helped elucidate the immunity of survivors.

Additionally, the LSA platform offers investigators the most resolved view of the epitope the location an antibody binds to its target. An epitope is an innate property that cannot be changed and must be discovered empirically. The LSA is the only technology that enables characterization of epitope binding at the full library level.

The world is in need of a solution to COVID-19, says Josh Eckman, Carterras Chief Executive Officer. Were honored to be the provider of high-throughput antibody screening and characterization data to CoVIC. They have the most ambitious research goals and aggressive timelines. The Carterra LSA is the right tool at the right time.

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Carterra to Provide Antibody Screening and Characterization for the Coronavirus Immunotherapy Consortium (CoVIC) - Technology Networks