Wicher K, Wicher V
Wadsworth Center for Labs and Research, New York State Department of Health, Albany.
Crit Rev Microbiol. 1989;16(3):181-234. doi: 10.3109/10408418909104471.
The infrequent use of guinea pig in experimental syphilis, the not well genetically and immunologically characterized strains of animals originating from places with unspecified conditions of husbandry, and the various strains of Treponema pallidum used for infection provided inconsistent and discouraging results. For eight decades the rabbit has been the major animal model in studies of syphilis. However, the lack of readily available inbred strains of rabbits--necessary for adoptive transfer experiments--has been a stumbling block in revealing the mechanisms responsible for immunity, susceptibility, and resistance to T. pallidum infection. These difficulties have recently been overcome by demonstration of inbred strains susceptible to T. pallidum infection, paving the way to studies of adoptive immunity. The guinea pig may also be a better model than the rabbit for immunomanipulations (irradiation, injection with antibodies specific to various cell populations), allowing a closer insight into the immunopathologic mechanism operating during the course of syphilitic infection. The "rediscovery" of the guinea pig as a model for experimental syphilis and recent years of intensive studies justify a review summarizing older data and providing the most recent information. The authors, having first-hand experience with this model, will provide detailed information on (1) historical background; (2) course of infection with T. pallidum in inbred and outbred strains of guinea pigs; (3) the ID50 for various strains; (4) various routes of infection; (5) age and sex-dependent susceptibility to infection; (6) kinetic of the humoral response to specific and non-specific treponemal antigens; (7) appearance of autoantibodies and immune complexes; (8) cellular response, including lymphoproliferative response, macrophage inhibitory factor(s) production, chemotaxis and adoptive transfer of immunity by purified T cells; and (9) a complete list of references.
豚鼠在实验性梅毒研究中使用频率较低,源自饲养条件不明地区的动物菌株在遗传和免疫方面特征不佳,以及用于感染的梅毒螺旋体菌株各异,这些都导致了结果不一致且令人沮丧。八十年来,兔子一直是梅毒研究中的主要动物模型。然而,缺乏易于获得的近交系兔子(这是过继转移实验所必需的)一直是揭示梅毒螺旋体感染免疫、易感性和抗性机制的绊脚石。最近,通过证明存在对梅毒螺旋体感染敏感的近交系,这些困难已被克服,为过继免疫研究铺平了道路。豚鼠在免疫操作(辐射、注射针对各种细胞群体的特异性抗体)方面可能也是比兔子更好的模型,这使得我们能够更深入地了解梅毒感染过程中运作的免疫病理机制。豚鼠作为实验性梅毒模型的“重新发现”以及近年来的深入研究,使得有必要进行一次综述,总结旧数据并提供最新信息。作者对该模型有第一手经验,将提供有关以下方面的详细信息:(1)历史背景;(2)豚鼠近交系和远交系感染梅毒螺旋体的过程;(3)各种菌株的半数感染剂量(ID50);(4)各种感染途径;(5)年龄和性别依赖性感染易感性;(6)对特异性和非特异性梅毒螺旋体抗原的体液反应动力学;(7)自身抗体和免疫复合物的出现;(8)细胞反应,包括淋巴细胞增殖反应、巨噬细胞抑制因子的产生、趋化作用以及纯化T细胞的免疫过继转移;(9)完整的参考文献列表。