Update on Chlamydia trachomatis Vaccinology

被引:5
|
作者
de la Maza, Luis M. [1 ]
Zhong, Guangming [2 ]
Brunham, Robert C. [3 ]
机构
[1] Univ Calif Irvine, Dept Pathol & Lab Med, Irvine, CA 92717 USA
[2] Univ Texas Hlth Sci Ctr San Antonio, Dept Microbiol & Immunol, San Antonio, TX 78229 USA
[3] Univ British Columbia, Ctr Dis Control, Vaccine Res Lab, Vancouver, BC, Canada
关键词
Chlamydia trachomatis vaccines; Chlamydia muridarum; antigens; adjuvants; routes of immunization; delivery systems; Chlamydia trachomatis vaccinology; OUTER-MEMBRANE-PROTEIN; GENITAL-TRACT INFECTION; PELVIC-INFLAMMATORY-DISEASE; MOUSE PNEUMONITIS BIOVAR; T-CELL ANTIGENS; OBLIGATE INTRACELLULAR PATHOGEN; ENDOGENOUS GAMMA-INTERFERON; PROTECTIVE IMMUNE-RESPONSE; GENOME-WIDE IDENTIFICATION; CROSS-SEROVAR PROTECTION;
D O I
10.1128/CVI.00543-16
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Attempts to produce a vaccine to protect against Chlamydia trachomatis-induced trachoma were initiated more than 100 years ago and continued for several decades. Using whole organisms, protective responses were obtained. However, upon exposure to C. trachomatis, disease exacerbation developed in some immunized individuals, precluding the implementation of the vaccine. Evidence of the role of C. trachomatis as a sexually transmitted pathogen started to emerge in the 1960s, and it soon became evident that it can cause acute infections and long-term sequelae in women, men, and newborns. The main focus of this minireview is to summarize recent findings and discuss formulations, including antigens, adjuvants, routes, and delivery systems for immunization, primarily explored in the female mouse model, with the goal of implementing a vaccine against C. trachomatis genital infections.
引用
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页数:25
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