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

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Blood, 1 February 2003, Vol. 101, No. 3, pp. 1024-1029

IMMUNOBIOLOGY

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

From the Department of Microbiology and Immunology and Department of Medicine, Drexel University College of Medicine, Drexel University, Philadelphia, PA; and Department of Microbiology and Immunology, Emory University, Atlanta, GA.

HIV-specific CD8+ T cells are prone to undergo apoptosis, and this may affect their ability to control HIV infection. Because 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 interleukin 15 (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, interferon gamma  (IFNgamma ) 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.

© 2003 by The American Society of Hematology.
 

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