The multifactorial nature of HIV-1 latency

Trends Mol Med. 2004 Nov;10(11):525-31. doi: 10.1016/j.molmed.2004.09.006.

Abstract

HIV-1 can avoid host immune responses and antiretroviral drugs through the latent infection of resting memory CD4(+) T cells. Recently, latent viral genomes have been shown to reside within the introns of active host genes. Therefore, latency is not simply due to an inaccessibility of the integrated proviruses to the transcriptional machinery. Rather, latency might result from insufficient nuclear levels of the crucial activation-dependent host transcription factors required to overcome the transcriptional interference that is an automatic consequence of the nature of HIV-1 integration sites. In addition, resting cells lack sufficient levels of HIV-1 Tat and Tat-associated activation-dependent host factors that are necessary for processive transcription. Defects at consecutive steps of transcriptional initiation and elongation enable HIV-1 to remain hidden within resting CD4(+) T cells.

Publication types

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

MeSH terms

  • CD4-Positive T-Lymphocytes / virology
  • Gene Expression Regulation, Viral*
  • HIV Infections / virology*
  • HIV-1 / genetics*
  • HIV-1 / physiology
  • Humans
  • Proviruses / genetics
  • Proviruses / physiology
  • Transcription Factors / genetics*
  • Transcription Factors / physiology
  • Transcription, Genetic
  • Virus Integration / genetics*
  • Virus Latency / genetics*
  • Virus Latency / physiology

Substances

  • Transcription Factors