A combination of broadly neutralizing HIV-1 monoclonal antibodies targeting distinct epitopes effectively neutralizes variants found in early infection

J Virol. 2012 Oct;86(19):10857-61. doi: 10.1128/JVI.01414-12. Epub 2012 Jul 25.

Abstract

Neutralizing antibody protection against HIV-1 may require broad and potent antibodies targeting multiple epitopes. We tested 7 monoclonal antibodies (MAbs) against 45 viruses of diverse subtypes from early infection. The CD4 binding site MAb NIH45-46W was most broad and potent (91% coverage; geometric mean 50% inhibitory concentration [IC(50)], 0.09 μg/ml). Combining NIH45-46W and a V3-specific MAb, PGT128, neutralized 96% of viruses, while PGT121, another V3-specific MAb, neutralized the remainder. Thus, 2 or 3 antibody specificities may prevent infection by most HIV-1 variants.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies / chemistry
  • Antibodies, Monoclonal / chemistry
  • Antibodies, Neutralizing
  • Antibody Specificity
  • CD4 Antigens / biosynthesis
  • Cluster Analysis
  • Epitopes / chemistry*
  • HIV Antibodies / chemistry*
  • HIV Infections / immunology*
  • HIV Infections / virology
  • HIV-1 / immunology
  • Humans
  • Inhibitory Concentration 50
  • Neutralization Tests
  • Polysaccharides / chemistry

Substances

  • Antibodies
  • Antibodies, Monoclonal
  • Antibodies, Neutralizing
  • CD4 Antigens
  • Epitopes
  • HIV Antibodies
  • Polysaccharides