Prognostic value of HIV-1 Gag-specific CD4+ T-cell responses for progression to AIDS analyzed in a prospective cohort study

被引:30
作者
Jansen, CA
De Cuyper, IM
Hooibrink, B
van der Bij, AK
van Baarle, D
Miedema, F
机构
[1] Univ Utrecht, Med Ctr, Dept Immunol, NL-3508 AB Utrecht, Netherlands
[2] Univ Amsterdam, Acad Med Ctr, Sanquin Res & Landsteiner Lab, Dept Clin Viroimmunol, NL-1105 AZ Amsterdam, Netherlands
[3] Univ Amsterdam, Acad Med Ctr, Dept Cell Biol & Histol, NL-1105 AZ Amsterdam, Netherlands
[4] Univ Amsterdam, Dept HIV & STI Res, Municipal Hlth Serv, NL-1105 AZ Amsterdam, Netherlands
关键词
D O I
10.1182/blood-2005-07-2907
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The causal relationship between HIV-specific CD4(+) T-cell responses and viral control and the effect of these responses on the natural history of HIV infection is unclear. In a detailed longitudinal study, functional HIV-1 Gag-specific CD4(+) T cells were analyzed in long-term asymptomatic individuals (LTA; n = 6) and progressors to AIDS (n = 7) with a median follow-up of, respectively, 118 and 57 months. Next, HIV-specific CD4+ T-helper cell responses were measured in a prospective cohort study among 96 HIV seroconverters and were related to clinical endpoints using Cox proportional hazard analyses. In the detailed study, no difference for HIV-specific helper-cell responses between LTAs and progressors was observed early in infection, but Gagspecific CD4(+) T cells producing IL-2 or IFN gamma were lost in progressors late in infection. Multivariate proportional hazard analyses in the prospective cohort study showed that HIV-specific IL-2(+), IFN gamma(+), or IL-2(+)IFN gamma(+) CD4(+) T cells early after seroconversion had no prognostic value for the rate of progression to AIDS. Our results are compatible with viral load determining the nature and magnitude of HIV-specific CD4(+) T-cell responses, rather than HIV-specific CD4(+) T-cell responses controlling HIV plasma viral load.
引用
收藏
页码:1427 / 1433
页数:7
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