Macrophage immunoregulatory pathways in tuberculosis

被引:107
|
作者
Rajararna, Murugesan V. S. [1 ]
Ni, Bin [1 ]
Dodd, Claire E. [1 ,2 ]
Schlesinger, Larry S. [1 ,2 ]
机构
[1] Ohio State Univ, Dept Microbial Infect & Immun, Ctr Microbial Interface Biol, Columbus, OH 43210 USA
[2] Ohio State Univ, Dept Microbiol, Columbus, OH 43210 USA
关键词
Macrophages; Innate immunity; Pattern recognition receptors; MicroRNAs; Lung; SURFACTANT PROTEIN-A; ACTIVATED RECEPTOR-GAMMA; BACILLUS-CALMETTE-GUERIN; PATTERN-RECOGNITION RECEPTOR; HUMAN ALVEOLAR MACROPHAGES; INNATE IMMUNE-RESPONSE; NITRIC-OXIDE SYNTHASE; BETA-GLUCAN RECEPTOR; INHIBITS CYTOKINE PRODUCTION; MYCOBACTERIUM-BOVIS BCG;
D O I
10.1016/j.smim.2014.09.010
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Macrophages, the major host cells harboring Mycobacterium tuberculosis (M.tb), are a heterogeneous cell type depending on their tissue of origin and host they are derived from. Significant discord in macrophage responses to M.tb exists due to differences in M.tb strains and the various types of macrophages used to study tuberculosis (TB). This review will summarize current concepts regarding macrophage responses to M.tb infection, while pointing out relevant differences in experimental outcomes due to the use of divergent model systems. A brief description of the lung environment is included since there is increasing evidence that the alveolar macrophage (AM) has immunoregulatory properties that can delay optimal protective host immune responses. In this context, this review focuses on selected macrophage immunoregulatory pattern recognition receptors (PRRs), cytokines, negative regulators of inflammation, lipid mediators and microRNAs (miRNAs). (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:471 / 485
页数:15
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