Turning foes into permissive hosts: manipulation of macrophage polarization by intracellular bacteria

被引:5
|
作者
Pham, Trung H. M. [1 ,2 ]
Monack, Denise M. [1 ]
机构
[1] Stanford Univ, Dept Microbiol & Immunol, Sch Med, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Pediat, Sch Med, Stanford, CA 94305 USA
关键词
NITRIC-OXIDE SYNTHASE; ALTERNATIVE ACTIVATION; TUBERCULOSIS INFECTION; STAT3; ACTIVATION; GENE-EXPRESSION; PPAR-GAMMA; IFN-GAMMA; REPLICATION; RECOGNITION; MECHANISMS;
D O I
10.1016/j.coi.2023.102367
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 function as tissue-immune sentinels and mediate key antimicrobial responses against bacterial pathogens. Yet, they can also act as a cellular niche for intracellular bacteria, such as Salmonella entenca, to persist in infected tissues. Macrophages exhibit heterogeneous activation or polarization, states that are linked to differential antibacterial responses and bacteria permissiveness. Remarkably, recent studies demonstrate that Salmonella and other intracellular bacteria inject virulence effectors into the cellular cytoplasm to skew the macrophage polarization state and reprogram these immune cells into a permissive niche. Here, we review mechanisms of macrophage reprogramming by Salmonella and highlight manipulation of macrophage polarization as a shared bacterial pathogenesis strategy. In addition, we discuss how the interplay of bacterial effector mechanisms, microenvironmental signals, and ontogeny may shape macrophage cell states and functions. Finally, we propose ideas of how further research will advance our understanding of macrophage functional diversity and immunobiology.
引用
收藏
页数:9
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