Department of Molecular Sciences and Pediatrics, University of Tennessee Health Science Center, Memphis, TN 38163, USA.
J Infect Dis. 2010 Jun 15;201 Suppl 2:S96-103. doi: 10.1086/652393.
Chlamydia trachomatis is an important cause of sexually transmitted infection that can manifest as acute cervicitis, pelvic inflammatory disease, and most commonly, chronic asymptomatic infection. The basis of this wide spectrum of manifestations and the factors that lead to clearance or chronic infection are poorly understood. We reviewed specific literature pertaining to clearance of primary genital tract infections in animal models, including mice, guinea pigs, pigs, sheep, and nonhuman primates. T helper 1 cell responses involved in cell-mediated immunity are key immune parameters that define efficient clearance in the murine and guinea pig models of chlamydial infection, which are useful for studying C. trachomatis clearance. However, there may be some differences between humans and other animals in innate and adaptive immune responses to chlamydial infection. Studies have suggested that differences in the induced T cell subsets and the species-specific differences in interferon gamma-mediated effector mechanisms may play a significant role in these discrepancies. To close these gaps in knowledge, translational research in humans is a critical next step. However, for questions about specific mechanisms of host-pathogen interaction that cannot be answered feasibly or ethically in humans, animal models will continue to be important. Future research should include use of humanized and nonmurine models that establish prolonged infection to improve understanding of chronic human infections.
沙眼衣原体是一种重要的性传播感染病原体,可表现为急性宫颈炎、盆腔炎,最常见的是慢性无症状感染。这种广泛的临床表现基础以及导致清除或慢性感染的因素尚不清楚。我们回顾了与动物模型(包括小鼠、豚鼠、猪、绵羊和非人灵长类动物)中原发性生殖道感染清除相关的特定文献。细胞介导免疫中涉及的辅助性 T 细胞 1 型反应是定义小鼠和豚鼠衣原体感染清除的关键免疫参数,这些模型对于研究沙眼衣原体清除很有用。然而,人类与其他动物对衣原体感染的固有和适应性免疫反应可能存在一些差异。研究表明,诱导的 T 细胞亚群的差异以及干扰素 γ介导的效应机制的种属特异性差异可能在这些差异中起重要作用。为了缩小这些知识差距,在人类中进行转化研究是至关重要的下一步。然而,对于那些在人体中无法或不道德地回答的关于宿主-病原体相互作用的具体机制问题,动物模型仍将是重要的。未来的研究应包括使用人源化和非鼠类模型来建立持续性感染,以提高对慢性人类感染的理解。