Innate and Adaptive Cellular Immune Responses to Mycobacterium tuberculosis Infection

被引:123
作者
Mayer-Barber, Katrin D. [1 ]
Barber, Daniel L. [2 ]
机构
[1] NIAID, Immunobiol Sect, Parasit Dis Lab, NIH, 9000 Rockville Pike, Bethesda, MD 20892 USA
[2] NIAID, Lymphocyte Biol Unit T, Parasit Dis Lab, NIH, 9000 Rockville Pike, Bethesda, MD 20892 USA
关键词
CD4(+) T-CELLS; NITRIC-OXIDE SYNTHASE; IMMUNODEFICIENCY-VIRUS-INFECTION; PNEUMOCYSTIS-CARINII-PNEUMONIA; LUNG DENDRITIC CELLS; W-BEIJING STRAINS; IN-VIVO DEPLETION; PULMONARY TUBERCULOSIS; INTERFERON-GAMMA; IFN-GAMMA;
D O I
10.1101/cshperspect.a018424
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Host resistance to Mycobacterium tuberculosis (Mtb) infection requires the coordinated efforts of innate and adaptive immune cells. Diverse pulmonary myeloid cell populations respond to Mtb with unique contributions to both host-protective and potentially detrimental inflammation. Although multiple cell types of the adaptive immune system respond to Mtb infection, CD4 T cells are the principal antigen-specific cells responsible for containment of Mtb infection, but they can also be major contributors to disease during Mtb infection in several different settings. Here, we will discuss the role of different myeloid populations as well as the dual nature of CD4 T cells in Mtb infection with a primary focus on data generated using in vivo cellular immunological studies in experimental animal models and in humans when available.
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页数:19
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