Immunoepidemiologic profile of Chlamydia trachomatis infection:: Importance of heat-shock protein 60 and interferon-γ

被引:103
作者
Cohen, CR
Koochesfahani, KM
Meier, AS
Shen, CX
Karunakaran, K
Ondondo, B
Kinyari, T
Mugo, NR
Nguti, R
Brunham, RC
机构
[1] Univ Calif San Francisco, Dept Obstet Gynecol & Reprod Sci, San Francisco, CA 94105 USA
[2] Univ Washington, Dept Lab Med, Seattle, WA 98195 USA
[3] Fred Hutchinson Canc Res Ctr, Program Biostat, Seattle, WA 98104 USA
[4] Univ British Columbia, Ctr Dis Control, Vancouver, BC V5Z 1M9, Canada
[5] Univ Nairobi, Dept Med Microbiol, Nairobi, Kenya
[6] Univ Nairobi, Dept Physiol, Nairobi, Kenya
[7] Univ Nairobi, Dept Obstet & Gynecol, Nairobi, Kenya
[8] Univ Nairobi, Dept Stat, Nairobi, Kenya
基金
美国国家卫生研究院; 加拿大健康研究院;
关键词
D O I
10.1086/432070
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Epidemiological, animal, and in vitro investigations suggest that Chlamydia trachomatis infection engenders acquired immunity, the basis for which is incompletely defined, especially in humans. In a prospective cohort study of women at high risk for C. trachomatis infection, we found that, at baseline and after adjustment for age and other potential confounding variables, production of interferon-gamma by peripheral-blood mononuclear cells (PBMCs) stimulated with chlamydia heat-shock protein 60 strongly correlated with protection against incident C. trachomatis infection. This investigation supports a direct role for C. trachomatis-specific immune responses in altering the risk of infection and suggests immune correlates of protection that are potentially useful in vaccine development.
引用
收藏
页码:591 / 599
页数:9
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