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Human combinatorial libraries yield rare antibodies that broadly neutralize hepatitis C virus

Johansson, Daniel X.; Voisset, Cécile; Tarr, Alexander W.; Aung, Mie; Ball, Jonathan K.; Dubuisson, Jean; Persson, Mats A.A.

Authors

Daniel X. Johansson

Cécile Voisset

Mie Aung

JONATHAN BALL jonathan.ball@nottingham.ac.uk
Professor of Molecular Virology

Jean Dubuisson

Mats A.A. Persson



Abstract

One way to dissect the antibody response to an invading microorganism is to clone the antibody repertoire from immune donors and subsequently characterize the specific antibodies. Recently, methodological advances have allowed investigations of neutralizing antibodies against hepatitis C virus (HCV) in vitro. We have investigated three human mAbs, previously isolated from an individual infected with HCV of genotype 2b, that are known to cross-react in a binding assay to the envelope E2 protein of genotypes 1a and 1b. We now report that two of them have a neutralizing activity with a breadth not previously observed. Indeed, mAbs 1:7 and A8 recognized E2 from all of the six major genotypes, and they neutralized retroviral pseudoparticles [HCV pseudoparticles (HCVpp)] carrying genetically equally diverse HCV envelope glycoproteins. Importantly, these antibodies were also able to neutralize the cell culture infectious HCV clone JFH-1 in vitro, with IC50 values of 60 ng/ml and 560 ng/ml, respectively. The conformational epitopes of these two broadly reactive antibodies were overlapping yet distinct and involved amino acid residues in the 523-535 region of E2, known to be important for the E2-CD81 interaction. The third antibody clone, representing a dominant population in the initial screen for these antibodies, was less broadly reactive and was unable to neutralize the genotype 2a infectious clone JFH-1. Our results confirm at the clonal level that broadly neutralizing human anti-HCV antibodies can be elicited and that the region amino acids 523-535 of the HCV envelope glycoprotein E2 carries neutralizing epitopes conserved across all genotypes. © 2007 by The National Academy of Sciences of the USA.

Citation

Johansson, D. X., Voisset, C., Tarr, A. W., Aung, M., Ball, J. K., Dubuisson, J., & Persson, M. A. (2007). Human combinatorial libraries yield rare antibodies that broadly neutralize hepatitis C virus. Proceedings of the National Academy of Sciences, 104(41), 16269-16274. https://doi.org/10.1073/pnas.0705522104

Journal Article Type Article
Publication Date Oct 9, 2007
Deposit Date Nov 9, 2022
Journal Proceedings of the National Academy of Sciences
Print ISSN 0027-8424
Electronic ISSN 1091-6490
Publisher National Academy of Sciences
Peer Reviewed Peer Reviewed
Volume 104
Issue 41
Pages 16269-16274
DOI https://doi.org/10.1073/pnas.0705522104
Public URL https://nottingham-repository.worktribe.com/output/3129609
Publisher URL https://www.pnas.org/doi/full/10.1073/pnas.0705522104