New insights into HIV-1 specific cytotoxic T-lymphocyte responses in exposed, persistently seronegative Kenyan sex workers

被引:89
作者
Kaul, R [1 ]
Rowland-Jones, SL
Kimani, J
Fowke, K
Dong, T
Kiama, P
Rutherford, J
Njagi, E
Mwangi, F
Rostron, T
Onyango, J
Oyugi, J
MacDonald, KS
Bwayo, JJ
Plummer, FA
机构
[1] Univ Nairobi, Dept Med Microbiol, Nairobi, Kenya
[2] John Radcliffe Hosp, Inst Mol Med, MRC, Human Immunol Unit, Oxford OX3 9DS, England
[3] Univ Manitoba, Dept Med Microbiol, Winnipeg, MB, Canada
[4] Univ Toronto, Mt Sinai Hosp, Dept Microbiol, Toronto, ON M5G 1X5, Canada
基金
英国医学研究理事会;
关键词
HIV-1; cytotoxic T-lymphocytes; seroconversion; epitopes;
D O I
10.1016/S0165-2478(01)00260-7
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A clearer understanding of HIV-1 specific immune responses in highly-exposed, persistently seronegative (HEPS) subjects is important in developing models of HIV-1 protective immunity. HIV-1 specific cytotoxic T-lymphocytes (CTL) have been described in a cohort of HEPS Kenyan sex workers, and recent work has further elucidated these responses. CTL specific for HIV-1 Env were found in the blood of over half the sex workers meeting criteria for HIV resistance, and in some women recognized unmapped epitopes. The proportion of women with Env-specific CTL increased with the duration of uninfected HIV exposure, suggesting that these responses were acquired over time. CD8 + lymphocyte responses directed against predefined HIV-1 CTL epitopes from various HIV-1 genes were found in the blood and genital tract of > 50% resistant sex workers, at a ten-fold lower frequency than in infected subjects. The epitope specificity of CD8 + responses differs between HEPS and HIV infected women, and in HEPS the maintenance of responses appears to be dependent on persistent HIV exposure. Several HIV-1 'resistant' sex workers have become HIV infected over the past 6 years, possibly related to waning of pre-existing HIV-specific CTL, and infection has often been associated with a switch in the epitope specificity of CD8 + responses. These findings suggest that vaccine-induced protective HIV immunity is a realistic goal, but that vaccine strategies of boosting or persistent antigen may be necessary for long-lived protection. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:3 / 13
页数:11
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