Important note: Information in this article was accurate in 1995. The state of the art may have changed since the publication date.
Diminished V beta T cell subset responses to superantigen in HIV+ individuals as determined by multiparameter flow cytometry.
Natl Conf Hum Retroviruses Relat Infect (2nd). 1995 Jan 29-Feb 2;:86. Unique Identifier : AIDSLINE AIDS/95920206 Maino V; Ruitenberg JJ; Suni MA; Mole L; Holodniy M; Becton Dickinson Immunocytometry Systems, San Jose, CA.
Abstract:
Staphylococcal enterotoxins represent a class of superantigens characterized by an ability to stimulate subsets of T cells expressing unique families of T cell receptor beta chains (TCR V beta) in a manner that is dependent on class II MHC. We have recently developed a multiparameter flow cytometric method for rapidly assessing individual lymphocyte subset responses to a variety of stimuli including superantigen. The assay was utilized to monitor the expression of an early activation marker (CD69) in whole blood samples after 4 hour incubation with superantigens with specificities for T cell subsets expressing a range of TCR V beta variable region families. In whole blood samples obtained from normal donors staphylococcal enterotoxin B (SEB) stimulated CD69 expression on V beta 6 expressing CD4+ T cells but did not stimulate T cells expressing V beta 8 consistent with the specificity reported for this superantigen. In an effort to explore superantigen responses in HIV+ individuals we analyzed CD4+ and CD8+ T cell subsets in normal and seropositive donors for the expression of CD69 following stimulation with SEB using 3-color flow cytometry. Percent positive CD69 expression on specific T cell subsets was related to stage of disease (CD4 counts) and various clinical parameters including identified opportunistic infections. Preliminary studies indicated that a number of samples from HIV+ individuals exhibited significantly diminished responses to SEB compared to normal controls as determined by percentage of CD4+ and CD8+ T cells expressing CD69. This difference was most apparent within the CD8+ T cell population. Longitudinal studies in HIV subjects are currently in progress to examine individual V beta T cell subset responses to superantigen.
Keywords: Flow Cytometry Human HIV Seropositivity/*IMMUNOLOGY Superantigens/*IMMUNOLOGY *T-Lymphocyte Subsets ABSTRACT 951230
M95C2931
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