Evidence for circulating activated cytotoxic T cells in HIV-infected subjects before the onset of opportunistic infections
- PMID: 2208794
- PMCID: PMC1535171
- DOI: 10.1111/j.1365-2249.1990.tb05395.x
Evidence for circulating activated cytotoxic T cells in HIV-infected subjects before the onset of opportunistic infections
Abstract
The activity of both cytotoxic T lymphocyte (CTL) and natural killer (NK) cells were measured cross-sectionally in 43 subjects seropositive for HIV, in 27 HIV- blood donors and in 24 HIV- persons from the Outpatients Clinic for sexually transmitted diseases. CTL activity was evaluated using the HL-60 cells coated with OKT3 as the targets and freshly separated peripheral blood lymphocytes as the effectors. In 20 out of 43 HIV+ subjects, CTL activity was significantly enhanced in comparison to the HIV- subjects. This lytic activity correlated positively with the percentages of CD3+ HLA-DR+, of CD8+ CR3- and of CD57+ CD16- lymphocytes, and was greatly reduced after elimination of CD8+, of HLA-DR+ or of CD57+ cells. The median CTL activity seemed to increase from CDC group II to CDC group IV (Centers for Disease Control classification), but to return back to control levels in those patients with a history of opportunistic infections. NK function in HIV+ subjects was not significantly different from that in the blood donors. In seropositive patients, NK activity correlated positively with the percentages of both CD16+ CD57+ and of CD8+ CR3+ cells and was strongly diminished after elimination of CD16+ or of CD57+ cells. There was no significant change in NK function according to the clinical stage. The data show that circulating CD8+ HLA-DR+ CD57+ T cells in HIV+ subjects are activated cytotoxic T cells and point to progressive (over) activation of this T cell compartment until the onset of opportunistic infections.
Similar articles
-
Lack of correlation between phenotype activation markers of CD8 lymphocytes and cytotoxic T lymphocyte (CTL) function in HIV-1 infection: evidence for rescue with rIL-2.Viral Immunol. 1994;7(2):81-95. doi: 10.1089/vim.1994.7.81. Viral Immunol. 1994. PMID: 7848511
-
Evidence of a selective depletion of a CD16+ CD56+ CD8+ natural killer cell subset during HIV infection.Cytometry. 1995 Mar 15;22(1):10-5. doi: 10.1002/cyto.990220103. Cytometry. 1995. PMID: 7587727
-
IL-7 enhancement of antigen-driven activation/expansion of HIV-1-specific cytotoxic T lymphocyte precursors (CTLp).Clin Exp Immunol. 1995 Aug;101(2):239-48. doi: 10.1111/j.1365-2249.1995.tb08345.x. Clin Exp Immunol. 1995. PMID: 7544247 Free PMC article.
-
HLA-class I-specific inhibitory receptors in HIV-1 infection.Hum Immunol. 2000 Jan;61(1):74-81. doi: 10.1016/s0198-8859(99)00169-x. Hum Immunol. 2000. PMID: 10658980 Review.
-
Lymphocyte subsets as surrogate markers in antiretroviral therapy.Infection. 1991;19 Suppl 2:S103-8. doi: 10.1007/BF01644477. Infection. 1991. PMID: 1826674 Review.
Cited by
-
Subset markers of CD8(+) cells and their relation to enhanced cytotoxic T-cell activity during human immunodeficiency virus infection.J Clin Immunol. 1991 Nov;11(6):345-56. doi: 10.1007/BF00918800. J Clin Immunol. 1991. PMID: 1761640
-
Cytotoxic activity against maedi-visna virus-infected macrophages.J Virol. 1994 Dec;68(12):8331-8. doi: 10.1128/JVI.68.12.8331-8338.1994. J Virol. 1994. PMID: 7966626 Free PMC article.
-
Trisomy 7 and trisomy 10 characterize subpopulations of tumor-infiltrating lymphocytes in kidney tumors and in the surrounding kidney tissue.Proc Natl Acad Sci U S A. 1992 Oct 15;89(20):9744-8. doi: 10.1073/pnas.89.20.9744. Proc Natl Acad Sci U S A. 1992. PMID: 1409692 Free PMC article.
-
The effects of depression, stressful life events, social support, and coping on the progression of HIV infection.Curr Psychiatry Rep. 2000 Dec;2(6):495-502. doi: 10.1007/s11920-000-0008-4. Curr Psychiatry Rep. 2000. PMID: 11123001 Review.
-
Increased cytolytic T lymphocyte activity and decreased B7 responsiveness are associated with CD28 down-regulation on CD8+ T cells from HIV-infected subjects.Clin Exp Immunol. 1995 Jun;100(3):425-33. doi: 10.1111/j.1365-2249.1995.tb03717.x. Clin Exp Immunol. 1995. PMID: 7539725 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Research Materials