Vaccination against Chlamydia Genital Infection Utilizing the Murine C-muridarum Model

被引:95
作者
Farris, Christina M. [2 ]
Morrison, Richard P. [1 ]
机构
[1] Univ Arkansas Med Sci, Dept Microbiol & Immunol, Little Rock, AR 72205 USA
[2] Univ Alabama Birmingham, Dept Microbiol, Birmingham, AL 35294 USA
基金
美国国家卫生研究院;
关键词
OUTER-MEMBRANE PROTEIN; PROTECTIVE IMMUNE-RESPONSE; CD4(+) T-CELLS; TRACT INFECTION; INTRANASAL IMMUNIZATION; GAMMA-INTERFERON; TRACHOMATIS INFECTION; CHOLERA-TOXIN; MUCOSAL IMMUNIZATION; ANTIBODY-RESPONSES;
D O I
10.1128/IAI.00881-10
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Chlamydia trachomatis genital infection is a worldwide public health problem, and considerable effort has been expended on developing an efficacious vaccine. The murine model of C. muridarum genital infection has been extremely useful for identification of protective immune responses and in vaccine development. Although a number of immunogenic antigens have been assessed for their ability to induce protection, the majority of studies have utilized the whole organism, the major outer membrane protein ( MOMP), or the chlamydial protease-like activity factor (CPAF). These antigens, alone and in combination with a variety of immunostimulatory adjuvants, have induced various levels of protection against infectious challenge, ranging from minimal to nearly sterilizing immunity. Understanding of the mechanisms of natural infection-based immunity and advances in adjuvant biology have resulted in studies that are increasingly successful, but a vaccine licensed for use in humans has not yet been brought to fruition. Here we review immunity to chlamydial genital infection and vaccine development using the C. muridarum model.
引用
收藏
页码:986 / 996
页数:11
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