The multifactorial nature of HIV-1 latency

Kara Lassen, Yefei Han, Yan Zhou, Janet Siliciano, Robert F. Siliciano

Research output: Contribution to journalReview articlepeer-review

199 Scopus citations


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.

Original languageEnglish (US)
Pages (from-to)525-531
Number of pages7
JournalTrends in Molecular Medicine
Issue number11
StatePublished - Nov 2004

ASJC Scopus subject areas

  • Molecular Medicine
  • Molecular Biology


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