Functional HIV-1 specific IgA antibodies in HIV-1 exposed, persistently IgG seronegative female sex workers

被引:88
作者
Broliden, K
Hinkula, J
Devito, C
Kiama, P
Kimani, J
Trabbatoni, D
Bwayo, JJ
Clerici, M
Plummer, F
Kaul, R
机构
[1] Huddinge Univ Hosp, Karolinska Inst, Dept Clin Virol, S-14186 Huddinge, Sweden
[2] Karolinska Inst, Dept Clin Virol, Swedish Inst Infect Dis Control, Ctr Microbiol & Tumor Biol, S-10521 Stockholm, Sweden
[3] Univ Nairobi, Dept Med Microbiol, Nairobi, Kenya
[4] Univ Milan, Chair Immunol, Milan, Italy
[5] Univ Manitoba, Dept Med Microbiol, Winnipeg, MB, Canada
[6] John Radcliffe Hosp, Inst Mol Med, MRC, Human Immunol Unit, Oxford OX3 9DU, England
基金
英国医学研究理事会;
关键词
HIV resistance; humoral immunity; neutralization; transcytosis;
D O I
10.1016/S0165-2478(01)00263-2
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Although HIV-specific cellular immune responses are found in a number of HIV highly-exposed, persistently seronegative (HEPS) cohorts, late seroconversion can occur despite pre-existing cytotoxic T lymphocytes (CTL), suggesting that a protective HIV vaccine may need to induce a broader range of HIV-specific immune responses. Low levels of HIV-specific IgA have been found in the genital tract and plasma of the majority of Nairobi HEPS sex workers and appeared to be independent of HIV-specific cellular responses. IgA purified from genital tract, saliva and plasma of most HEPS sex workers were able to neutralize infection of PBMC by a primary (NSI) clade B HIV isolate, as well as viral isolates from clades A and D, which predominate in Kenya. In addition, these IgA were able to inhibit transcytosis of infective HIV virions across a transwell model of the human mucosal epithelium in an HIV-specific manner. Preliminary work in other HEPS cohorts has suggested the recognition of different gp41 epitopes in HEPS and HIV-infected subjects. Although present at low levels, these IgA demonstrated cross-clade neutralizing activity and were able to inhibit HIV mucosal transcytosis, suggesting an important functional role in protection against HIV infection. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:29 / 36
页数:8
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