Winslow Gary M, Bitsaktsis Constantine
Wadsworth Center, New York State Department of Health, Albany, New York 12208, USA.
Curr Opin Infect Dis. 2005 Jun;18(3):217-21. doi: 10.1097/01.qco.0000168381.86024.cf.
Discusses recent developments in the study of immunity and host defense against the monocytic ehrlichiae in 2003 and 2004. The review does not address anaplasmoses, as the anaplasmae were recently re-classified into the genus Anaplasma, and are distinct in cell tropism from the ehrlichiae.
The features of the immune responses against these emerging Gram-negative obligate intracellular pathogens are only beginning to be understood. Important advances in our ability to study host defense include the development of new experimental mouse models. Recent studies have defined possible mechanisms of innate immune subversion in human monocytes, as well as roles for lymphocyte subsets and type I cytokines during mouse infection. Other studies in the mouse suggest that cytokine production by CD8 T cells may contribute to immunopathology. New data also support a role for humoral immunity during host defense against these intracellular pathogens.
The use of new animal models will facilitate research of the mechanisms of innate, adaptive, and pathological immune responses, and will enhance our understanding of human immunity to the ehrlichiae as well as to other pathogenic intracellular bacteria.
讨论2003年和2004年关于单核细胞埃立克体免疫及宿主防御研究的最新进展。由于无形体最近被重新分类到无形体属,并且在细胞嗜性方面与埃立克体不同,因此本综述不涉及无形体病。
针对这些新出现的革兰氏阴性专性细胞内病原体的免疫反应特征才刚刚开始被了解。我们研究宿主防御能力的重要进展包括新实验小鼠模型的开发。最近的研究已经确定了人类单核细胞中先天性免疫颠覆的可能机制,以及小鼠感染期间淋巴细胞亚群和I型细胞因子的作用。小鼠的其他研究表明,CD8 T细胞产生的细胞因子可能导致免疫病理学。新数据也支持体液免疫在宿主抵御这些细胞内病原体过程中的作用。
新动物模型的使用将有助于研究先天性、适应性和病理性免疫反应的机制,并将增进我们对人类对埃立克体以及其他致病性细胞内细菌的免疫的理解。