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

被引:13
作者
Ozawa, Tatsuhiko [1 ]
Jin, Aishun [1 ]
Tajiri, Kazuto [1 ,2 ]
Takemoto, Masaya [3 ]
Okuda, Tomoko [3 ]
Shiraki, Kimiyasu [3 ]
Kishi, Hiroyuki [1 ]
Muraguchi, Atsushi [1 ]
机构
[1] Toyama Univ, Dept Immunol, Grad Sch Med & Pharmaceut Sci, Toyama 9300194, Japan
[2] Toyama Univ, Dept Internal Med 3, Grad Sch Med & Pharmaceut Sci, Toyama 9300194, Japan
[3] Toyama Univ, Dept Virol, Grad Sch Med & Pharmaceut Sci, Toyama 9300194, Japan
关键词
Influenza; M2e-antibody; Antibody therapeutics; INTEGRAL MEMBRANE-PROTEIN; M2; PROTEIN; M-GENE; VACCINE; MICE; ECTODOMAIN; IMMUNIZATION; OSELTAMIVIR; M2-PROTEIN; AMANTADINE;
D O I
10.1016/j.antiviral.2011.06.012
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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.
引用
收藏
页码:283 / 287
页数:5
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