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Prepublished online as a Blood First Edition Paper on September 19, 2002; DOI 10.1182/blood-2002-07-1957.

Submitted July 2, 2002
Accepted September 4, 2002
IL-15 enhances survival and function of HIV-specific CD8+ T cells
Yvonne M Mueller, Paul M Bojczuk, E Scott Halstead, Alfred H J Kim, James Witek, John D Altman, and Peter D Katsikis*
Department of Microbiology and Immunology, Drexel University College of Medicine, Philadelphia, PA, USA
Department of Medicine, Drexel University College of Medicine, Philadelphia, PA, USA
Department of Microbiology and Immunology, Emory University, Atlanta, GA, USA
* Corresponding author; email: katsikis{at}drexel.edu.
HIV-specific CD8+ T cells are prone to undergo apoptosis and this may affect their ability to control HIV infection. Since CD8-mediated immune responses play a key role in controlling HIV infection, enhancing the survival and effector function of HIV-specific CD8+ T cells may augment their ability to control HIV virus. We show here that IL-15 potently inhibits spontaneous and CD95/Fas-induced apoptosis of HIV-specific CD8+ T cells. IL-15 inhibits apoptosis in both CD45RA-CD62L- and CD45RA+CD62L- effector memory subpopulations of these cells. Furthermore, IL-15 greatly enhances the survival of HIV-specific CD8+ T cells in long-term cultures. Finally, IL-15 directly enhances activation, IFN production and direct ex vivo cytotoxicity of HIV-specific CD8+ T cells. Thus, IL-15 potently enhances the survival and effector function of HIV-specific CD8+ T cells and therefore may prove useful in augmenting the antiviral function of these cells.

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