Neutralizing Antibody-Based Prevention of Cell-Associated HIV-1 Infection

Viruses. 2018 Jun 18;10(6):333. doi: 10.3390/v10060333.

Abstract

Improved vaccine-mediated protection against HIV-1 requires a thorough understanding of the mode of HIV-1 transmission and how various immune responses control transmission. Cell-associated HIV-1 is infectious and contributes to HIV-1 transmission in humans. Non-human primate models of cell-associated SIV infection demonstrate that cell-associated SIV is more infectious than cell-free SIV. In a recently described chimeric simian⁻human immunodeficiency virus (SHIV) macaque model, it was demonstrated that an occult infection with cell-associated SHIV can be established that evades passive protection with a broadly neutralizing antibody (bnAb). Indeed, considerable in vitro data shows that bnAbs have less efficacy against cell-associated HIV-1 than cell-free HIV-1. Optimizing the protective capacity of immune responses such as bnAbs against cell-associated infections may be needed to maximize their protective efficacy.

Keywords: HIV-1; broadly neutralizing antibody; cell-associated virus; simian–human immunodeficiency virus.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Antibodies, Neutralizing / immunology*
  • Disease Models, Animal
  • Disease Transmission, Infectious / prevention & control*
  • HIV Antibodies / immunology*
  • HIV Infections / prevention & control*
  • HIV Infections / transmission*
  • HIV-1 / immunology*
  • Immunization, Passive
  • Macaca

Substances

  • Antibodies, Neutralizing
  • HIV Antibodies