Methodology

A focus reduction neutralization assay for hepatitis C virus neutralizing antibodies

Carole Fournier¹ , Gilles Duverlie¹ , Catherine François¹ , Aurelie Schnuriger² , Sarah Dedeurwaerder¹ , Etienne Brochot¹ , Dominique Capron³ , Czeslaw Wychowski⁴ , Vincent Thibault² and Sandrine Castelain¹

¹  Laboratoire de Virologie, Centre Hospitalo-Universitaire, Amiens, France

²  Laboratoire de Virologie, CERVI, Hôpital Pitié-Salpêtrière, Paris, France

³  Service d'Hépatologie, Centre Hospitalo-Universitaire, Amiens, France

⁴  Unité d'assemblage et de réplication du virus de l'hépatite C, CNRS-UMR 8161, Institut de Biologie de Lille, Lille, France

author email corresponding author email

Virology Journal 2007, 4:35doi:10.1186/1743-422X-4-35

Published:	30 March 2007

Abstract

Background/Aim

The role of humoral immunity in hepatitis C virus (HCV) infection is poorly understood. Nevertheless, there is increasing interest in characterizing the neutralizing antibodies in the serum of HCV-infected patients. Focus reduction assays have been widely used to evaluate neutralizing antibody responses against a range of non-cytopathic viruses. Based on the recent development of a HCV cell culture system using the genotype 2 JFH-1-strain, we developed a focus reduction assay for HCV-neutralizing antibodies.

Methods

The focus reduction assay was based on a standard microneutralization assay in which immunostained foci on tissue culture plates are counted. The neutralizing anti-HCV antibodies titers of purified serum immunoglobulin samples from seventy-seven individuals were determined using a 50% focus reduction neutralization assay. Each titer was determined as the log value of the reciprocal antibody dilution that reduced the number of viral foci by 50%. IgG antibodies were first purified from each serum in order to avoid the facilitating effect of HDL on HCV entry.

Results

The assay's cut-off using an ELISA and RNA HCV-negative samples was found to be 1.25 log, corresponding to a dilution of 1:18. The assay was compared with a commercial HCV ELISA and exhibited specificity and sensitivity values of 100% and 96.5%, respectively, and good reproducibility (with intra-assay and inter-assay coefficients of variation of 6.7% and 12.6%, respectively). The assay did not show any cross-reactivity with anti-HIV, anti-HBs or heterophile antibody-positive samples. The neutralizing antibodies titers were 2.13 log (1:134) for homologous samples from HCV genotype 2 infected patients harboring the same genotype as JFH-1 and 1.93 log (1:85) for heterologous samples from patients infected by genotypes other than type 2. These results confirm the presence of broadly cross-neutralizing antibodies already reported using the HCV pseudoparticles system.

Conclusion

This study presents a simple, specific and reproducible cell culture-based assay for determination of HCV-neutralizing antibodies in human sera. The assay should be an important tool for gauging the relationship between the neutralizing antibodies response and viral load kinetics in acutely or chronically infected patients and for investigating the possible eradication or prevention of HCV infection by neutralizing antibodies.