Determinants of HIV-specific CD8 T-cell responses in HIV-infected pediatric patients and enhancement of HIV-gag-specific responses with exogenous IL-15

被引:27
作者
Chitnis, V
Pahwa, R
Pahwa, S [1 ]
机构
[1] NYU, Sch Med, Immunol & Inflammat Ctr Excellence, N Shore Long Isl Jewish Res Inst, Manhasset, NY 11030 USA
[2] NYU, Sch Med, N Shore Univ Hosp, Div Pediat Immunol, Manhasset, NY 11030 USA
关键词
D O I
10.1016/S1521-6616(02)00051-7
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Cellular immune responses play a central role in controlling HIV-1 infection. HIV-specific IFN-gamma production by CD8 T cells was evaluated in 17 HLA-A2+ HIV-infected pediatric patients (age range I month to 16 years) in an ELISPOT assay. Most patients (15/17) exhibited responses to HIV-gag, followed by responses to envelope gp120, gp41, and V3 loop. Only 7 patients responded to all four antigenic peptides. Treatment-related immune reconstitution of CD4 T cells was associated with increase in gag-specific responses, but these declined with prolonged viral suppression. Exogenous IL-15 resulted in augmentation of HIV-gag-specific response in 71% of patients, while IL-2 and IL-7 had variable effects, augmenting responses in 25% patients. Thus, HIV-specific CD8 T-cell responses are dependent on both CD4 T-cell help and antigenic stimulation. The cytokine IL-15 may be a useful modality as adjunctive therapy to augment HIV-specific memory CD8 T cells. (C) 2003 Elsevier Science (USA). All rights reserved.
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页码:36 / 45
页数:10
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