| Literature DB >> 21726583 |
Tatsuhiko Ozawa1, Aishun Jin, Kazuto Tajiri, Masaya Takemoto, Tomoko Okuda, Kimiyasu Shiraki, Hiroyuki Kishi, Atsushi Muraguchi.
Abstract
The extra-cellular domain of the influenza virus matrix protein 2 (M2e) is highly conserved between influenza A virus strains compared to hemagglutinin and neuraminidase, and has long been viewed as a potential and universal vaccine target. M2e induces no or only weak and transient immune responses following infection, making it difficult to detect M2e-specific antibodies producing B-cells in human peripheral blood lymphocytes. Recently, using a single-cell manipulation method, immunospot array assay on a chip (ISAAC), we obtained an M2e-specific human antibody (Ab1-10) from the peripheral blood of a healthy volunteer. In this report, we have demonstrate that Ab1-10 reacted not only to seasonal influenza A viruses, but also to pandemic (H1N1) 2009 virus (2009 H1N1) and highly pathogenic avian influenza A virus, and that the antibody-bound M2e of 2009 H1N1 inactivated the virus with high affinity (∼10(-10)M). More importantly, it inhibited 2009 H1N1 viral propagation in vitro. These results suggest that Ab1-10 might be a potential candidate for antibody therapeutics for a wide range of influenza A viruses.Entities:
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Year: 2011 PMID: 21726583 DOI: 10.1016/j.antiviral.2011.06.012
Source DB: PubMed Journal: Antiviral Res ISSN: 0166-3542 Impact factor: 5.970