Murthy Ashlesh K, Cong Yu, Murphey Cathi, Guentzel M Neal, Forsthuber Thomas G, Zhong Guangming, Arulanandam Bernard P
Department of Biology, University of Texas at San Antonio, 6900 North Loop 1604 West, San Antonio, TX 78249, USA.
Infect Immun. 2006 Dec;74(12):6722-9. doi: 10.1128/IAI.01119-06. Epub 2006 Oct 2.
There is no licensed vaccine available against Chlamydia trachomatis, the leading cause of bacterial sexually transmitted disease. We have found that intranasal immunization with recombinant chlamydial protease-like activity factor (CPAF) induces CD4(+) T-cell- and gamma interferon (IFN-gamma)-dependent protective immunity against murine genital chlamydial infection, thus making CPAF a viable vaccine candidate for further characterization. HLA-DR4 is the predominant allele involved in chlamydial antigen presentation to CD4(+) T cells in humans. We used engineered mice that lack endogenous major histocompatibility complex class II (MHC-II) alleles but express a human HLA allele (HLA-DR4 transgenic [tg] mice) to examine primary immune and CPAF-mediated responses against genital Chlamydia muridarum challenge. Upon primary bacterial exposure, HLA-DR4 tg mice developed Chlamydia-specific IFN-gamma and antibody production and resolved the infection within 30 days, similar to challenged conventional C57BL/6 animals. Moreover, C. muridarum-challenged HLA-DR4 tg mice exhibited CPAF-specific antibody and IFN-gamma production. Upon CPAF-plus-interleukin-12 (IL-12) vaccination, HLA-DR4 tg animals exhibited robust CPAF-specific IFN-gamma production and elevated titers of anti-CPAF total antibody and immunoglobulin G2a (IgG2a) and lower titers of IgG2b and IgG1 antibodies. HLA-DR4 tg and C57BL/6 mice vaccinated with CPAF plus IL-12 resolved the primary genital chlamydial infection significantly earlier than mock-immunized animals, whereas similarly vaccinated MHC class II-deficient mice displayed minimal antigen-specific immune responses and failed to resolve the infection even at 30 days postchallenge. Together, these results demonstrate the importance of human HLA-DR4 molecules in the recognition and presentation of CPAF epitopes, leading to the generation of protective antichlamydial immunity and making these mice a valuable model for mapping HLA-DR4-restricted chlamydial epitopes.
针对细菌性性传播疾病的主要病原体沙眼衣原体,目前尚无获得许可的疫苗。我们发现,用重组衣原体蛋白酶样活性因子(CPAF)进行鼻内免疫可诱导CD4(+) T细胞和γ干扰素(IFN-γ)依赖性的针对小鼠生殖器衣原体感染的保护性免疫,因此使CPAF成为进一步鉴定的可行疫苗候选物。HLA-DR4是人类中参与衣原体抗原呈递给CD4(+) T细胞的主要等位基因。我们使用缺乏内源性主要组织相容性复合体II类(MHC-II)等位基因但表达人类HLA等位基因的工程小鼠(HLA-DR4转基因[tg]小鼠),来研究针对生殖器鼠衣原体攻击的初次免疫和CPAF介导的反应。初次接触细菌后,HLA-DR4 tg小鼠产生了衣原体特异性IFN-γ和抗体,并在30天内清除了感染,这与受到攻击的常规C57BL/6动物相似。此外,受到鼠衣原体攻击的HLA-DR4 tg小鼠表现出CPAF特异性抗体和IFN-γ的产生。在CPAF加白细胞介素-12(IL-12)疫苗接种后HLA-DR4 tg动物表现出强大的CPAF特异性IFN-γ产生,抗CPAF总抗体和免疫球蛋白G2a(IgG2a)滴度升高,而IgG2b和IgG1抗体滴度降低。用CPAF加IL-12接种的HLA-DR4 tg和C57BL/6小鼠比假免疫动物更早地清除了原发性生殖器衣原体感染,而同样接种疫苗的MHC II类缺陷小鼠表现出最小的抗原特异性免疫反应,甚至在攻击后30天仍未能清除感染。总之,这些结果证明了人类HLA-DR4分子在识别和呈递CPAF表位中的重要性,导致产生保护性抗衣原体免疫,并使这些小鼠成为绘制HLA-DR4限制性衣原体表位的有价值模型。