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IMMUNE DEREGULATION IN CONGENITAL HIV DISEASE

$0M01FY2002RRNIH

Weill Medical College Of Cornell Univ, New York NY

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Abstract

In the HIV infected neonate, opportunistic infections may develop in children with normal T-lymphocyte subset number and even in the absence of an inverted CD4/CD8 ration. Recent studies have suggested that these critical differences may be related to alteratios in cytokine production. We propose to evaluate: 1. shifts in lymphocyte subpopulations specificallysubpopulations of CD8+ cell subsets and CD4+T cell. 2. Responsiveness to immune system activators specifically Interleukin-2, as reflected in proliferation, expression of the IL-2 receptor, IL-2 production, and HIV viral activation. 3. Serum levels of prostaglandin, (PGE-2) which may cause down regulation of the cytokine network. 4. The ability of lymphocytes form HIV exposed infants to mediate natural killer (NK) activity in vitro.

View original record on NIH RePORTER →