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Prevention of HIV-1 infection in chimpanzees by gpl20 V3 domain-specific monoclonal antibody

  • E. A. Emini
  • , W. A. Schleif
  • , J. H. Nunberg
  • , A. J. Conley
  • , Y. Eda
  • , S. Tokiyoshi
  • , S. D. Putney
  • , S. Matsushita
  • , K. E. Cobb
  • , C. M. Jett
  • , J. W. Eichberg
  • , K. K. Murthy

Research output: Contribution to journalArticlepeer-review

473 Scopus citations

Abstract

THE acquired immunodeficiency syndrome (AIDS) is the late-stage clinical manifestation of long-term persistent infection with the human immunodeficiency virus type 1 (HIV-1). Immune responses directed against the virus and against virus-infected cells during the persistent infection fail to mediate resolution of the infection. As a result, a successful AIDS vaccine must elicit an immune state that will prevent the establishment of the persistent infection following introduction of the virus into the host. The third hyper-variable (V3) domain of the HIV-1 gp120 envelope glycoprotein is a disulphide-linked closed loop of about 30 amino acids which binds and elicits anti-HIV-1 type-specific virus-neutralizing antibodies1-7. The in vitro characteristics of anti-V3 domain antibody suggest that this antibody could by itself prevent HIV-1 infection in vivo8,9, an idea supported by chimpanzee challenge studies in which protection against the HIV-1 persistent infection seemed to correlate with the presence of anti-V3 domain antibody10-12. Here we directly demonstrate the protective efficacy of anti-V3 domain antibody in vivo and propose that this antibody is potentially useful as both a pre- and post-exposure prophylactic agent.

Original languageEnglish
Pages (from-to)728-730
Number of pages3
JournalNature
Volume355
Issue number6362
DOIs
StatePublished - 1992

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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