4.7 Article

Characterization of a fully human monoclonal antibody against extracellular domain of matrix protein 2 of influenza A virus

Journal

ANTIVIRAL RESEARCH
Volume 91, Issue 3, Pages 283-287

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.antiviral.2011.06.012

Keywords

Influenza; M2e-antibody; Antibody therapeutics

Funding

  1. Hokuriku Innovation Cluster for Health Science Project
  2. Ministry of Education, Culture, Sports and Science, Japan
  3. Toyama and Ishikawa Prefectures
  4. Grants-in-Aid for Scientific Research [23390264] Funding Source: KAKEN

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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 (similar to 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. (C) 2011 Elsevier B.V. All rights reserved.

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