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The present study describes the persistent expansion of a subpopulation of circulating double-positive CD4+CD8+ T cells in a human immunodeficiency virus (HIV)-infected person over 8 years. The percentage of double-positive cells was remarkably stable with time and was not related to HIV plasma virus load. CD4+CD8+ cells exhibited phenotypic characteristics of activated memory T lymphocytes. Analysis of V beta usage by the T cell receptors of these cells indicated restricted expression to the V beta 14 and V beta 17 families. Most CD4+CD8+ cells constitutively expressed cytotoxicity-associated molecules (C1.7 and perforin) and were selectively committed to produce interferon-gamma and tumor necrosis factor-alpha, cytokines involved in cytotoxic function. The kinetics of changes in the relative proportion of single-positive CD4+ and double-positive CD4+CD8+ T cell subsets and a similar bias in V beta usage by these subsets suggest that CD4+CD8+ lymphocytes originate from peripheral expansion of mature CD4+ T cells.

the journal of infectious diseases (online. university of chicago press)/the journal of infectious diseases

Persistent Expansion, in a Human Immunodeficiency Virus‐Infected Person, of Vb‐Restricted CD4<sup>+</sup>CD8<sup>+</sup>T Lymphocytes that Express Cytotoxicity‐Associated Molecules and Are Committed to Produce Interferon‐γ and Tumor Necrosis Factor‐α

Persistent Expansion, in a Human Immunodeficiency Virus‐Infected Person, of Vb‐Restricted CD4+CD8+T Lymphocytes that Express Cytotoxicity‐Associated Molecules and Are Committed to Produce Interferon‐γ and Tumor Necrosis Factor‐α

Persistent Expansion, in a Human Immunodeficiency Virus‐Infected Person, of Vb‐Restricted CD4⁺CD8⁺T Lymphocytes that Express Cytotoxicity‐Associated Molecules and Are Committed to Produce Interferon‐γ and Tumor Necrosis Factor‐α