Back to Search Start Over

Broad neutralization coverage of HIV by multiple highly potent antibodies.

Authors :
Walker LM
Huber M
Doores KJ
Falkowska E
Pejchal R
Julien JP
Wang SK
Ramos A
Chan-Hui PY
Moyle M
Mitcham JL
Hammond PW
Olsen OA
Phung P
Fling S
Wong CH
Phogat S
Wrin T
Simek MD
Koff WC
Wilson IA
Burton DR
Poignard P
Source :
Nature [Nature] 2011 Sep 22; Vol. 477 (7365), pp. 466-70.
Publication Year :
2011

Abstract

Broadly neutralizing antibodies against highly variable viral pathogens are much sought after to treat or protect against global circulating viruses. Here we probed the neutralizing antibody repertoires of four human immunodeficiency virus (HIV)-infected donors with remarkably broad and potent neutralizing responses and rescued 17 new monoclonal antibodies that neutralize broadly across clades. Many of the new monoclonal antibodies are almost tenfold more potent than the recently described PG9, PG16 and VRC01 broadly neutralizing monoclonal antibodies and 100-fold more potent than the original prototype HIV broadly neutralizing monoclonal antibodies. The monoclonal antibodies largely recapitulate the neutralization breadth found in the corresponding donor serum and many recognize novel epitopes on envelope (Env) glycoprotein gp120, illuminating new targets for vaccine design. Analysis of neutralization by the full complement of anti-HIV broadly neutralizing monoclonal antibodies now available reveals that certain combinations of antibodies should offer markedly more favourable coverage of the enormous diversity of global circulating viruses than others and these combinations might be sought in active or passive immunization regimes. Overall, the isolation of multiple HIV broadly neutralizing monoclonal antibodies from several donors that, in aggregate, provide broad coverage at low concentrations is a highly positive indicator for the eventual design of an effective antibody-based HIV vaccine.<br /> (© 2011 Macmillan Publishers Limited. All rights reserved)

Details

Language :
English
ISSN :
1476-4687
Volume :
477
Issue :
7365
Database :
MEDLINE
Journal :
Nature
Publication Type :
Academic Journal
Accession number :
21849977
Full Text :
https://doi.org/10.1038/nature10373