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Protection from the 2009 H1N1 Pandemic Influenza by an Antibody from Combinatorial Survivor-Based Libraries
Author(s) -
A.K. Kashyap,
John Steel,
Adam Rubrum,
Angeles Estellés,
Raffaella Briante,
Natalia A. Ilyushina,
Xu Li,
Ryann E. Swale,
Aleksandr M. Faynboym,
Pamela K. Foreman,
Michael Horowitz,
Lawrence Horowitz,
Richard Webby,
Peter Palese,
Richard A. Lerner,
Ramesh R. Bhatt
Publication year - 2010
Publication title -
plos pathogens
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.719
H-Index - 206
eISSN - 1553-7374
pISSN - 1553-7366
DOI - 10.1371/journal.ppat.1000990
Subject(s) - reassortment , virology , pandemic , virus , influenza a virus , influenza a virus subtype h5n1 , biology , population , antibody , antigenic drift , immunology , disease , medicine , infectious disease (medical specialty) , covid-19 , environmental health , pathology
Influenza viruses elude immune responses and antiviral chemotherapeutics through genetic drift and reassortment. As a result, the development of new strategies that attack a highly conserved viral function to prevent and/or treat influenza infection is being pursued. Such novel broadly acting antiviral therapies would be less susceptible to virus escape and provide a long lasting solution to the evolving virus challenge. Here we report the in vitro and in vivo activity of a human monoclonal antibody (A06) against two isolates of the 2009 H1N1 pandemic influenza virus. This antibody, which was obtained from a combinatorial library derived from a survivor of highly pathogenic H5N1 infection, neutralizes H5N1, seasonal H1N1 and 2009 “Swine” H1N1 pandemic influenza in vitro with similar potency and is capable of preventing and treating 2009 H1N1 influenza infection in murine models of disease. These results demonstrate broad activity of the A06 antibody and its utility as an anti-influenza treatment option, even against newly evolved influenza strains to which there is limited immunity in the general population.

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