Effect of combination antiretroviral therapy upon rectal mucosal HIV RNA burden and mononuclear cell apoptosis

AIDS. 1998 Apr 16;12(6):597-604. doi: 10.1097/00002030-199806000-00008.

Abstract

Background: Pathogen-negative diarrhea is common in HIV infection and has been associated with clinical symptoms, histopathology, HIV expression, CD4+ lymphocyte depletion, cytokine mRNA expression, and apoptosis of lamina propria mononuclear cells.

Objectives and methods: To examine the short-term (7-day) effects of treatment with combination antiretroviral therapies upon gastrointestinal symptoms and rectal mucosa in 15 HIV-infected subjects.

Results: Treatment was associated with significant decreases in the perception of abdominal bloating and cramps. Similar declines in RNA burden and rises in CD4+ lymphocyte counts were found in blood and mucosa. Treatment was also associated with a fall in the number of lamina propria mononuclear cells undergoing apoptosis by in situ labeling, a change that correlated with the change in mucosal viral burden.

Conclusions: Peripheral blood and mucosal compartments are equally responsive to effective antiretroviral therapies. The detection of significant changes within 7 days of starting antiviral therapy implies that intestinal dysfunction may be a direct result of local HIV infection.

Publication types

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

MeSH terms

  • Anti-HIV Agents / administration & dosage*
  • Apoptosis / immunology
  • CD4 Lymphocyte Count
  • CD4-Positive T-Lymphocytes / immunology
  • CD8-Positive T-Lymphocytes / immunology
  • Colic / drug therapy
  • Drug Therapy, Combination
  • Female
  • Gastrointestinal Diseases / drug therapy
  • HIV Core Protein p24 / analysis
  • HIV Core Protein p24 / blood
  • HIV Infections / drug therapy*
  • HIV Infections / physiopathology
  • Humans
  • Intestinal Mucosa / immunology
  • Intestinal Mucosa / physiopathology
  • Intestinal Mucosa / virology*
  • Lymphocytes / immunology*
  • Male
  • Prospective Studies
  • RNA, Viral / analysis*
  • RNA, Viral / blood
  • Viral Load

Substances

  • Anti-HIV Agents
  • HIV Core Protein p24
  • RNA, Viral