Document 1018 DOCN M9541018 TI Differential priming to programmed cell death of superantigen-reactive lymphocytes of HIV patients. DT 9504 AU Gorla R; Imberti L; Prati E; Brugnoni D; Caligaris S; Cattaneo R; Albertini A; Primi D; Clinical Immunology Units, Spedali Civili of Brescia, Italy. SO AIDS Res Hum Retroviruses. 1994 Sep;10(9):1097-103. Unique Identifier : AIDSLINE MED/95127292 AB Programmed cell death or apoptosis has been shown to play a central role in CD4+ T cell depletion following HIV infection. Because most apoptotic signals are delivered through T cell receptor stimulation, we investigated whether T cell depletion in AIDS is a stochastic phenomenon or if it preferentially affects T cell subsets defined by their interaction with superantigens. To address this problem we have taken advantage of the exclusive property of superantigens to trigger T cells expressing selective sets of T cell receptor V beta elements. Here we report that CD4+ T cells from HIV-infected patients can proliferate in vitro to T cell receptor mobilization by some superantigens, but not others. Furthermore, the failure of T cells to respond to some superantigens was shown to be due to an active cell death process that differentially affected T cells capable of interacting with different superantigens. The selective programmed cell death priming of T cells responsive to particular superantigens, observed in this study, suggests that T cell depletion in HIV infection is not simply due to the cytopathic effect of the virus. The possible link between programmed cell death and T cell receptor variable regions suggested by the present experiments may help to better define current models of AIDS pathogenesis. DE Acquired Immunodeficiency Syndrome/*IMMUNOLOGY Apoptosis/*IMMUNOLOGY Cells, Cultured CD4-Positive T-Lymphocytes/*IMMUNOLOGY/PHYSIOLOGY Flow Cytometry Human HIV Seropositivity/*IMMUNOLOGY Lymphocyte Transformation Receptors, Antigen, T-Cell/IMMUNOLOGY Superantigens/*IMMUNOLOGY Support, Non-U.S. Gov't T-Lymphocyte Subsets/IMMUNOLOGY T-Lymphocytes/*IMMUNOLOGY/PHYSIOLOGY JOURNAL ARTICLE SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).