HIV-1 Transcription but Not Intact Provirus Levels are Associated With Systemic Inflammation

J Infect Dis. 2021 Jun 4;223(11):1934-1942. doi: 10.1093/infdis/jiaa657.

Abstract

Individuals infected with human immunodeficiency virus (HIV) 1 have increased inflammation, which has been associated with age-associated diseases. Plasma markers, cell-associated virus levels, and ability to stimulate RNA transcription in latently infected cell lines was examined in younger and older HIV-1-infected individuals with suppressed virus. Cell-associated RNA, but not intact provirus level, had positive correlation with plasma D-dimer levels. Compared with the younger group, the older group had higher D-dimer levels and a trend toward more cell-associated RNA but similar levels of intact proviruses. Even though all measured inflammatory markers were relatively higher in the older group, this greater inflammation did not induce more HIV-1 transcription in latently infected cell lines. Inflammation and HIV-1 RNA expression increase with age despite similar levels of intact infectious HIV DNA. While plasma inflammation is correlated with HIV-1 RNA expression in peripheral blood mononuclear cells, it does not induce HIV-1 transcription in latently infected cell lines.

Keywords: HIV-1 latency; accelerated aging; cell-associated HIV; inflammation; viral transcription.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Fibrin Fibrinogen Degradation Products
  • HIV Infections*
  • HIV-1* / genetics
  • Humans
  • Inflammation* / virology
  • Leukocytes, Mononuclear
  • Proviruses* / genetics
  • RNA, Viral
  • Virus Latency

Substances

  • Fibrin Fibrinogen Degradation Products
  • RNA, Viral
  • fibrin fragment D