Co Dominic O, Hogan Laura H, Kim Shin-Il, Sandor Matyas
Program in Cellular and Molecular Biology, University of Wisconsin-Madison, 53706, USA.
Clin Immunol. 2004 Nov;113(2):130-6. doi: 10.1016/j.clim.2004.08.012.
Chronic infection with mycobacteria is controlled by the formation of granulomas. The failure of granuloma maintenance results in reactivation of disease. Macrophages are the dominant cell type in granulomas, but CD4+ T cells are the master organizers of granuloma structure and function. Recent work points to an unrecognized role for nonspecific T cells in maintaining granuloma function in the chronic phase of infection. In addition, it has become clear that mycobacteria and host T cells collaborate in formation of granulomas. Further understanding of how nonspecific T cells contribute to granuloma formation, as well as how bacteria and T cells maintain a harmonious relationship over the life of the host, will facilitate the development of new strategies to treat mycobacterial disease.
分枝杆菌的慢性感染通过肉芽肿的形成得以控制。肉芽肿维持功能的失败会导致疾病复发。巨噬细胞是肉芽肿中的主要细胞类型,但CD4 + T细胞是肉芽肿结构和功能的主要组织者。最近的研究表明,非特异性T细胞在感染慢性期维持肉芽肿功能方面发挥着未被认识的作用。此外,已经明确分枝杆菌与宿主T细胞在肉芽肿形成过程中相互协作。进一步了解非特异性T细胞如何促进肉芽肿形成,以及细菌和T细胞如何在宿主生命周期内维持和谐关系,将有助于开发治疗分枝杆菌病的新策略。