Persistent T cell and B cell activities in the duodenal mucosa of AIDS patients

AIDS. 1998 Oct 1;12(14):1763-9. doi: 10.1097/00002030-199814000-00007.

Abstract

Objective: As HIV infection most commonly occurs via a mucosal surface, and as gastrointestinal symptoms are very frequent among HIV-infected patients, we investigated the functional properties of residual lymphocytes in the duodenal mucosa from HIV-infected individuals.

Design: Duodenal biopsies and blood samples were obtained from 19 HIV-infected patients [Centers for Disease Control and Prevention (CDC) stage III] and from 19 controls.

Methods: Phenotypic analysis of lymphocytes was performed by flow cytometry and/or immunocytochemistry. Interferon gamma (IFN-gamma), interleukin (IL) 4 and immunoglobulin secretions were analysed by enzyme-linked immunospot techniques. The phenotype of cytokine-producing cells was analysed by flow cytometry.

Results: The proportions of duodenal T lymphocytes from HIV-infected patients spontaneously secreting IFN-gamma or IL-4 were not lower than those from healthy controls. In patients with a high intestinal mucosal viral load, they were higher than in controls (P < 0.05). The proportions of immunoglobulin-secreting cells were significantly raised in HIV-infected patients for the three main isotypes.

Conclusions: T- and B-cell populations of the intestinal mucosa remain functional or are even activated in patients with AIDS, even when the numbers of both mucosal and circulating CD4+ lymphocytes are strongly decreased.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • B-Lymphocytes / immunology*
  • Biopsy
  • Cytokines / metabolism
  • Duodenum / immunology*
  • Female
  • Flow Cytometry
  • HIV Infections / immunology*
  • HIV Infections / virology
  • Humans
  • Immunity, Mucosal
  • Immunoenzyme Techniques
  • Immunoglobulins / biosynthesis
  • Immunohistochemistry
  • Immunophenotyping
  • Intestinal Mucosa / immunology*
  • Intestinal Mucosa / virology
  • Male
  • Middle Aged
  • T-Lymphocyte Subsets / immunology*
  • Viral Load

Substances

  • Cytokines
  • Immunoglobulins