Lefrançais Emma, Hudrisier Denis, Neyrolles Olivier, Behar Samuel M, Ernst Joel D
Institut de Pharmacologie et de Biologie Structurale, Université de Toulouse, CNRS, UPS, Toulouse, France.
Department of Microbiology, University of Massachusetts Chan Medical School, Worcester, MA, USA.
Nat Rev Immunol. 2025 Jun 13. doi: 10.1038/s41577-025-01192-z.
Mycobacterium tuberculosis, the bacterium that causes tuberculosis (TB), results in more human mortality than any other single pathogen, in part because of the lack of an effective vaccine. Although T cells are essential for immunity to TB, the mechanisms that provide protective immunity are poorly understood. In this Review, we describe current gaps in our knowledge about T cell-mediated immune responses to M. tuberculosis and discuss how recent technologies, including multiphoton intravital microscopy, spatial multiomics and high-resolution in vivo analyses of cell-cell interactions, may be used to gain insights that can inform the design of T cell-targeted TB vaccines.
结核分枝杆菌是导致结核病(TB)的细菌,其造成的人类死亡比任何其他单一病原体都多,部分原因是缺乏有效的疫苗。尽管T细胞对结核病免疫至关重要,但提供保护性免疫的机制仍知之甚少。在本综述中,我们描述了目前我们对结核分枝杆菌T细胞介导的免疫反应的认识差距,并讨论了如何利用包括多光子活体显微镜、空间多组学和细胞间相互作用的高分辨率体内分析在内的最新技术来获得见解,为靶向T细胞的结核病疫苗设计提供依据。