Rev activity determines sensitivity of HIV-1-infected primary T cells to CTL killing

Immunity. 2003 Feb;18(2):289-99. doi: 10.1016/s1074-7613(03)00031-1.

Abstract

The HIV Nef protein is thought to promote HIV immune evasion by downmodulating MHC-I and protecting infected cells from CTL killing. In addition, we demonstrated that Rev, an HIV regulatory protein needed for expression of the HIV late genes, can influence CTL killing. When Rev activity level was reduced by virtue of amino acid alterations in the Rev protein sequence, infected cells were more resistant to anti-Gag and anti-Env CTL killing. A screen of primary viral isolates revealed that viruses derived from asymptomatic, infected people had lower Rev activity, lower Gag levels, and greater resistance to anti-Gag CTL killing. Thus, rev alleles with low activity may have a selective advantage in infected people with effective immune responses.

Publication types

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

MeSH terms

  • Alleles
  • Amino Acid Sequence
  • Base Sequence
  • Cells, Cultured
  • Cytotoxicity Tests, Immunologic
  • DNA, Viral / genetics
  • Gene Products, rev / genetics
  • Gene Products, rev / metabolism*
  • Genes, rev
  • HIV Infections / immunology
  • HIV Infections / virology
  • HIV-1 / genetics
  • HIV-1 / immunology*
  • HIV-1 / metabolism*
  • Humans
  • Models, Immunological
  • Molecular Sequence Data
  • Sequence Homology, Amino Acid
  • T-Lymphocytes / immunology*
  • T-Lymphocytes / virology*
  • T-Lymphocytes, Cytotoxic / immunology*
  • rev Gene Products, Human Immunodeficiency Virus

Substances

  • DNA, Viral
  • Gene Products, rev
  • rev Gene Products, Human Immunodeficiency Virus