Diverging Effects of Human Recombinant Anti-Hepatitis C Virus (HCV) Antibody Fragments Derived from a Single Patient on the Infectivity of a Vesicular Stomatitis Virus/HCV Pseudotype

Author:

Burioni Roberto1,Matsuura Yoshiharu2,Mancini Nicasio1,Tani Hideki2,Miyamura Tatsuo3,Varaldo Pietro E.1,Clementi Massimo4

Affiliation:

1. Institute of Microbiology, University of Ancona, 60020 Ancona

2. Research Center for Emerging Infectious Diseases and Research Institute for Microbial Diseases, Osaka University, Osaka 565-0871

3. Department of Virology II, National Institute of Infectious Diseases, Tokyo, Japan

4. Università “Vita-Salute San Raffaele,” IRCCS Istituto Scientifico San Raffaele, 20132 Milan, Italy

Abstract

ABSTRACT Hepatitis C virus (HCV) is the major causative agent of blood-borne non-A, non-B hepatitis. Although a strong humoral response is detectable within a few weeks of primary infection and during viral persistence, the role played by antibodies against HCV envelope glycoproteins in controlling viral replication is still unclear. We describe how human monoclonal anti-HCV E2 antibody fragments isolated from a chronically HCV-infected patient differ sharply in their abilities to neutralize infection of HepG2 cells by a vesicular stomatitis virus pseudotype bearing HCV envelope glycoproteins. Two clones were able to neutralize the pseudotype virus at a concentration of 10 μg/ml, while three other clones completely lacked this activity. These data can explain the lack of protection and the possibility of reinfection that occur even in the presence of a strong antiviral antibody response.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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