Program in Cellular and Molecular Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
Immunol Rev. 2015 Mar;264(1):74-87. doi: 10.1111/imr.12274.
The adaptive immune response mediated by T cells is critical for control of Mycobacterium tuberculosis (M. tuberculosis) infection in humans. However, the M. tuberculosis antigens and host T-cell responses that are required for an effective adaptive immune response to M. tuberculosis infection are yet to be defined. Here, we review recent findings on CD4(+) and CD8(+) T-cell responses to M. tuberculosis infection and examine the roles of distinct M. tuberculosis-specific T-cell subsets in control of de novo and latent M. tuberculosis infection, and in the evolution of T-cell immunity to M. tuberculosis in response to tuberculosis treatment. In addition, we discuss recent studies that elucidate aspects of M. tuberculosis-specific adaptive immunity during human immunodeficiency virus co-infection and summarize recent findings from vaccine trials that provide insight into effective adaptive immune responses to M. tuberculosis infection.
T 细胞介导的适应性免疫反应对于控制人类结核分枝杆菌(Mycobacterium tuberculosis,M. tuberculosis)感染至关重要。然而,对于结核分枝杆菌感染产生有效适应性免疫反应所需的结核分枝杆菌抗原和宿主 T 细胞反应尚待确定。在此,我们回顾了近期关于结核分枝杆菌感染的 CD4(+)和 CD8(+)T 细胞反应的研究结果,并探讨了不同的结核分枝杆菌特异性 T 细胞亚群在控制初发和潜伏结核分枝杆菌感染以及在结核分枝杆菌治疗后结核分枝杆菌特异性 T 细胞免疫演变中的作用。此外,我们还讨论了阐明人类免疫缺陷病毒(human immunodeficiency virus,HIV)合并感染期间结核分枝杆菌特异性适应性免疫的最新研究,并总结了疫苗试验的最新发现,这些发现为理解结核分枝杆菌感染的有效适应性免疫反应提供了线索。
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