Functional T cell reconstitution and human immunodeficiency virus-1-specific cell-mediated immunity during highly active antiretroviral therapy

被引:102
作者
Pontesilli, O
Kerkhof-Garde, S
Notermans, DW
Foudraine, NA
Roos, MTL
Klein, MR
Danner, SA
Lange, JMA
Miedema, F
机构
[1] Univ Amsterdam, Dept Clin Viroimmunol, CLB Sanquin Blood Supply Fdn, NL-1012 WX Amsterdam, Netherlands
[2] Univ Amsterdam, Expt & Clin Immunol Lab, NL-1012 WX Amsterdam, Netherlands
[3] Univ Amsterdam, Div Infect Dis Trop Med & AIDS, NL-1012 WX Amsterdam, Netherlands
[4] Univ Amsterdam, Nalt AIDS Therapy Evaluat Ctr, Dept Internal Med, NL-1012 WX Amsterdam, Netherlands
[5] Univ Amsterdam, Dept Human Retrovirol, Acad Med Ctr, NL-1012 WX Amsterdam, Netherlands
关键词
D O I
10.1086/314837
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Lymphoproliferative responses (LPRs) to recall antigens (Ags) and human immunodeficiency virus type 1 (HIV-1) Gag and frequencies of circulating HIV-I-specific cytotoxic T lymphocyte precursors (CTLps) were measured in 12 patients undergoing highly active antiretroviral therapy (HAART) after long-standing HIV-1 infection. LPRs to at least 1 recall Ag became detectable or increased in all patients during HAART. No significant LPRs to Gag-p24 were observed, whereas 4 of 8 patients tested presented with Gag-p17-specific LPRs, HIV-1-specific CTLp frequencies became measurable or increased early during therapy in 6 of 10 patients tested and were maintained or decreased thereafter. Increasing HIV-l-specific CTLp frequencies were seen only in association with partial HAART failure in 1 patient. In conclusion, restoration of CD4(+) T lymphocyte responsiveness to recall Ags is achieved during HAART. The data provide evidence for limited HIV-1-specific CDC memory T cells during advanced HIV-1 infection and suggest that both CD4(+) and CD8(+) HIV-1-specific T cells are poorly stimulated when viral load is suppressed.
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页码:76 / 86
页数:11
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