Document 0037 DOCN M9490037 TI Major expansion of CD8+ T cells with a predominant V beta usage during the primary immune response to HIV [see comments] DT 9411 AU Pantaleo G; Demarest JF; Soudeyns H; Graziosi C; Denis F; Adelsberger JW; Borrow P; Saag MS; Shaw GM; Sekaly RP; et al; Laboratory of Immunoregulation, National Institute of Allergy and; Infectious Diseases, National Institutes of Health, Bethesda,; Maryland 20892. SO Nature. 1994 Aug 11;370(6489):463-7. Unique Identifier : AIDSLINE MED/94322938 CM Comment in: Nature 1994 Aug 11;370(6489):416 AB A SIGNIFICANT proportion (up to 70%) of individuals experience an acute clinical syndrome of varying severity associated with primary infection with the human immunodeficiency virus (HIV). We report here studies on six individuals who showed an acute HIV syndrome which generally resolved within four weeks, concomitant with a dramatic downregulation of viraemia. To characterize the T-cell-mediated primary immune response to HIV, we used combined semiquantitative polymerase chain reaction assay and cytofluorometry to analyse the T-cell antigen receptor repertoire in sequential peripheral blood mononuclear cells from the patients. We found major oligoclonal expansions in a restricted set of variable-domain beta-chain (V beta) families. Cells expressing the expanded V beta s predominantly expressed the CD8 T-cell differentiation antigen and mediated HIV-specific cytotoxicity. Major oligoclonal expansions of these CD8+ T lymphocytes may represent an important component of the primary immune response to viral infections and may help to clarify both the immunopathogenic and the protective mechanisms of HIV infection. DE Adolescence Adult Amino Acid Sequence *Antigens, CD8 Cell Line, Transformed Cells, Cultured Clone Cells Cytotoxicity, Immunologic DNA Female Flow Cytometry Human HIV/*IMMUNOLOGY HIV Infections/*IMMUNOLOGY Immunogenetics Immunophenotyping Male Molecular Sequence Data Polymerase Chain Reaction Prospective Studies Receptors, Antigen, T-Cell, alpha-beta/*GENETICS Support, Non-U.S. Gov't Support, U.S. Gov't, P.H.S. T-Lymphocyte Subsets/*IMMUNOLOGY JOURNAL ARTICLE SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).