Identification of a broadly cross-reacting and neutralizing human monoclonal antibody directed against the hepatitis C virus E2 protein

被引:109
作者
Perotti, Mario [1 ]
Mancini, Nicasio [1 ]
Diotti, Roberta A. [1 ]
Tarr, Alexander W. [2 ,3 ]
Ball, Jonathan K. [2 ,3 ]
Owsianka, Ania [4 ]
Adair, R. [4 ]
Patel, Arvind H. [4 ]
Clementi, Massimo [1 ]
Burioni, Roberto [1 ]
机构
[1] Univ Vita Salute San Raffale, Lab Microbiol & Virol, I-20132 Milan, Italy
[2] Univ Nottingham, Queens Med Ctr, Inst Infect Immun & Inflammat, Nottingham NG7 2UH, England
[3] Univ Nottingham, Queens Med Ctr, Div Microbiol, Nottingham NG7 2UH, England
[4] Univ Glasgow, Inst Virol, MRC Virol Unit, Glasgow G11 5JR, Lanark, Scotland
基金
英国医学研究理事会;
关键词
D O I
10.1128/JVI.01986-07
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Identification of anti-hepatitis C virus (anti-HCV) human antibody clones with broad neutralizing activity is important for a better understanding of the interplay between the virus and host and for the design of an effective passive immunotherapy and an effective vaccine. We report the identification of a human monoclonal Fab (e137) able to bind the HCV E2 glycoprotein of all HCV genotypes but genotype 5. The results of antibody competition assays and testing the reactivity to alanine mutant E2 proteins confirmed that the e137 epitope includes residues (T416, W420, W529, G530, and D535) highly conserved across all HCV genotypes. Fab e137 neutralized HCV pseudoparticles bearing genotype la, 1b, and 4 E1-E2 proteins and to a lesser extent, genotype 2b. Fab e137 was also able to inhibit cell culture-grown HCV (genotype 2a). These data indicate that broadly cross-reacting and cross-neutralizing antibodies are generated during HCV infection.
引用
收藏
页码:1047 / 1052
页数:6
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