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Advisor(s)
Abstract(s)
The effects of highly active antiretroviral therapy on cytokine imbalances associated with HIV-1 infection have not been characterized.
Using single cell analysis by flow cytometry, we show that a significant recovery in the frequency of IL-2-producing cells
was only observed in patients with a sustained control of viral replication and that the overexpanded CD8 T cell population of
CD282 IFN-g1 cells was not significantly reduced after 1 yr of effective therapy. Moreover, a detrimental role of IL-4 is suggested
by the association between an enhanced proportion of IL-4-producing cells within the CD4 and particularly the CD8 subset and
viral load rebound. Finally, the kinetics of changes of cell subsets assessed for simultaneous production of different cytokines
supports the view that cell reconstitution during highly active antiretroviral therapy is initially due to redistribution of terminally
differentiated cells, followed by peripheral expansion of less differentiated ones and a late progressive increase of the proportion
of functionally defined naive/memory precursor lymphocytes. These data bring new support for the role of cytokine imbalances
in AIDS pathogenesis and may be relevant for the definition of immunointervention targets.
Description
© 1999 by The American Association of Immunologists All rights reserved.
Keywords
Pedagogical Context
Citation
J Immunol 1999; 162:3718-3726
Publisher
American Association of Immunologists
