Immunological activation markers in the serum of African and European HIV-seropositive and seronegative individuals

AIDS. 1996 Nov;10(13):1535-42. doi: 10.1097/00002030-199611000-00012.

Abstract

Objective: The concentration of type 1 and type 2 cytokines and fibroblast-associated apoptosis-1 soluble receptor (sAPO-1/Fas) was analysed in the sera of Ugandan and Italian HIV-1-seropositive and seronegative individuals. The data were compared to determine whether the immunological status of these groups was different.

Methods: Sixty-seven Ugandan and 30 Italian HIV-positive patients were analysed and stratified according to CD4 counts (group 1, > 500 x 10(6)/l; group 2, 200-500 x 10(6)/l; group 3, < 200 x 10(6)/l). Sera from 15 Ugandan and 11 Italian HIV-negative blood donors were also analysed. Serum concentration of type 1 cytokines [interleukin (IL)-2, IL-12, and interferon (IFN)-gamma] and type 2 cytokines (IL-4 and IL-10), and sAPO-1/Fas were measured by enzyme-linked immunosorbent assay.

Results: Serum levels of IL-2, IFN-gamma and IL-10 but not of IL-4 and IL-12, were elevated in HIV-positive group 1 and 2 Africans compared with HIV-positive Italian individuals. IL-4 was mildly augmented in HIV-positive group 3 African patients. Serum concentration of sAPO-1/Fas was reduced in HIV-positive Africans compared with HIV-positive Italian individuals. Finally, serum levels of IL-2 and IL-10 were increased and sAPO-1/Fas reduced when sera of HIV-negative African healthy controls were compared with their Italian counterparts. The ratio of type 1/type 2 cytokines was roughly 1.0 in HIV-negative African controls, and much greater than 1.0 in HIV-negative Italian controls.

Conclusions: These preliminary findings indicate that immune activation is present in African HIV infection. Furthermore, these data raise the possibility that abnormal immune activation and increased susceptibility to antigen-induced cell death is present even in HIV-negative African controls.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AIDS-Related Opportunistic Infections / blood
  • AIDS-Related Opportunistic Infections / immunology
  • Adolescent
  • Adult
  • Animals
  • Cytokines / blood*
  • Female
  • HIV Seronegativity / immunology
  • HIV Seropositivity / blood
  • HIV Seropositivity / epidemiology
  • HIV Seropositivity / immunology*
  • Helminthiasis / blood
  • Helminthiasis / immunology
  • Humans
  • Interferon-gamma / blood
  • Interleukin-10 / blood
  • Interleukin-12 / blood
  • Interleukin-2 / blood
  • Interleukin-4 / blood
  • Italy / epidemiology
  • Male
  • Pilot Projects
  • Protozoan Infections / blood
  • Protozoan Infections / immunology
  • Tuberculosis / blood
  • Tuberculosis / immunology
  • Uganda / epidemiology
  • fas Receptor / blood*

Substances

  • Cytokines
  • Interleukin-2
  • fas Receptor
  • Interleukin-10
  • Interleukin-12
  • Interleukin-4
  • Interferon-gamma