Epitopes for broad and potent neutralizing antibody responses during chronic infection with human immunodeficiency virus type 1.

Published

Journal Article

Neutralizing antibody (nAb) response is sporadic and has limited potency and breadth during infection with human immunodeficiency virus type 1 (HIV-1). In rare cases, broad and potent nAbs are actually induced in vivo. Identifying specific epitopes targeted by such broad and potent nAb response is valuable in guiding the design of a prophylactic vaccine aimed to induce nAb. In this study, we have defined neutralizing epitope usage in 7 out of 17 subjects with broad and potent nAbs by using targeted mutagenesis in known neutralizing epitopes of HIV-1 glycoproteins and by using in vitro depletion of serum neutralizing activity by various recombinant HIV-1 glycoproteins. Consistent with recent reports, the CD4 binding site (CD4BS) is targeted by nAbs in vivo (4 of the 7 subjects with defined neutralizing epitopes). The new finding from this study is that epitopes in the gp120 outer domain are also targeted by nAbs in vivo (5 of the 7 subjects). The outer domain epitopes include glycan-dependent epitopes (2 subjects), conserved nonlinear epitope in the V3 region (2 subjects), and a CD4BS epitope composed mainly of the elements in the outer domain (1 subject). Importantly, we found indication for epitope poly-specificity, a dual usage of the V3 and CD4BS epitopes, in only one subject. This study provides a more complete profile of epitope usage for broad and potent nAb responses during HIV-1 infection.

Full Text

Duke Authors

Cited Authors

  • Nandi, A; Lavine, CL; Wang, P; Lipchina, I; Goepfert, PA; Shaw, GM; Tomaras, GD; Montefiori, DC; Haynes, BF; Easterbrook, P; Robinson, JE; Sodroski, JG; Yang, X; NIAID Center for HIV/AIDS Vaccine Immunology,

Published Date

  • January 20, 2010

Published In

Volume / Issue

  • 396 / 2

Start / End Page

  • 339 - 348

PubMed ID

  • 19922969

Pubmed Central ID

  • 19922969

Electronic International Standard Serial Number (EISSN)

  • 1096-0341

Digital Object Identifier (DOI)

  • 10.1016/j.virol.2009.10.044

Language

  • eng

Conference Location

  • United States