• Researchers identify potent antibody coc

    From ScienceDaily@1337:3/111 to All on Tue Jun 16 21:30:32 2020
    Researchers identify potent antibody cocktail to treat COVID-19
    Publication highlights process for yielding array of human antibodies
    that target protein on virus

    Date:
    June 16, 2020
    Source:
    University of Maryland School of Medicine
    Summary:
    Researchers evaluated several human antibodies to determine the
    most potent combination to be mixed in a cocktail and used as a
    promising anti-viral therapy against the virus that causes COVID-19.



    FULL STORY ========================================================================== Researchers at the University of Maryland School of Medicine
    (UMSOM) evaluated several human antibodies to determine the most
    potent combination to be mixed in a cocktail and used as a promising
    anti-viral therapy against the virus that causes COVID-19. Their research, conducted in collaboration with scientists at Regeneron Pharmaceuticals,
    was published in the journal Science. The study demonstrates the rapid
    process of isolating, testing and mass-producing antibody therapies
    against any infectious disease by using both genetically engineered mice
    and plasma from recovered COVID-19 patients.


    ==========================================================================
    The antibody cocktail evaluated by UMSOM researchers will be used to
    treat COVID-19 patients in a clinical trial that was launched last
    week. The study was funded by Regeneron, a biotechnology company based
    in Tarrytown, New York.

    Antibodies are proteins the immune system naturally makes in response
    to foreign invaders like viruses and bacteria. Antibody therapies were
    first tried in the late 19th century when researchers used a serum
    derived from the blood of infected animals to treat diphtheria.

    To produce the so-called monoclonal antibodies for an antibody cocktail to fight COVID-19, the researchers first needed to identify which antibodies
    fight the novel coronavirus most effectively.

    This involved determining which antibodies could bind most effectively
    to the spike protein found on the surface of SARS-CoV-2, the virus
    that causes COVID- 19. The Regeneron team evaluated thousands of human antibodies from plasma donations from recovered COVID-19 patients. They
    also generated antibodies from mice genetically engineered to produce
    human antibodies when infected with the virus.

    "The ability of the research team to rapidly derive antibodies using
    these two methods enabled us screen their selected antibodies against
    live virus to determine which had the strongest anti-viral effects," said
    study co-author Matthew Frieman, PhD, Associate Professor of Microbiology
    and Immunology at the University of Maryland School of Medicine. He has
    been studying coronaviruses for the past 16 years and has been carefully studying SARS-CoV-2 in his secure laboratory since February.

    Dr. Frieman and his UMSOM colleagues evaluated four of the most potent antibodies for to determine the potential of each one to neutralize
    the SARS- CoV-2 virus. They identified the two that would form the most powerful mix when used in combination.

    "An important goal of this research was to evaluate the most potent
    antibodies that bind to different molecules in the spike protein so
    they could be mixed together as a treatment," said study co-author
    Stuart Weston, PhD, a post- doctoral research fellow in the Department
    of Microbiology and Immunology.

    The cocktail containing the two antibodies is now being tested in a new clinical trial sponsored by Regeneron that will investigate whether the
    therapy can improve the outcomes of COVID-19 patients (both those who
    are hospitalized and those who are not). It will also be tested as a
    preventive therapy in those who are healthy but at high risk of getting
    sick because they work in a healthcare setting or have been exposed to
    an infected person.

    "Our School of Medicine researchers continue to provide vital advances
    on all fronts to help fight the COVID-19 pandemic and ultimately save
    lives," said Dean E. Albert Reece, MD, PhD, MBA, who is also Executive
    Vice President for Medical Affairs, UM Baltimore, and the John Z. and
    Akiko K. Bowers Distinguished Professor, University of Maryland School of Medicine. "This particular research not only contributes to a potential
    new therapy against COVID-19 but could have broader implications in terms
    of the development of monoclonal antibody therapies for other diseases."

    ========================================================================== Story Source: Materials provided by
    University_of_Maryland_School_of_Medicine. Note: Content may be edited
    for style and length.


    ========================================================================== Journal Reference:
    1. Johanna Hansen, Alina Baum, Kristen E. Pascal, Vincenzo Russo,
    Stephanie
    Giordano, Elzbieta Wloga, Benjamin O. Fulton, Ying Yan, Katrina
    Koon, Krunal Patel, Kyung Min Chung, Aynur Hermann, Erica Ullman,
    Jonathan Cruz, Ashique Rafique, Tammy Huang, Jeanette Fairhurst,
    Christen Libertiny, Marine Malbec, Wen-yi Lee, Richard Welsh,
    Glen Farr, Seth Pennington, Dipali Deshpande, Jemmie Cheng,
    Anke Watty, Pascal Bouffard, Robert Babb, Natasha Levenkova,
    Calvin Chen, Bojie Zhang, Annabel Romero Hernandez, Kei Saotome,
    Yi Zhou, Matthew Franklin, Sumathi Sivapalasingam, David Chien
    Lye, Stuart Weston, James Logue, Robert Haupt, Matthew Frieman,
    Gang Chen, William Olson, Andrew J. Murphy, Neil Stahl, George
    D. Yancopoulos, Christos A. Kyratsous. Studies in humanized mice
    and convalescent humans yield a SARS-CoV-2 antibody cocktail.

    Science, 2020; eabd0827 DOI: 10.1126/science.abd0827 ==========================================================================

    Link to news story: https://www.sciencedaily.com/releases/2020/06/200616135739.htm

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