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人体结核病的固有免疫防御:结核分枝杆菌与固有免疫细胞相互作用概述。

Innate Immune Defenses in Human Tuberculosis: An Overview of the Interactions between Mycobacterium tuberculosis and Innate Immune Cells.

机构信息

Emory Vaccine Center, Emory University, Atlanta, GA 30329, USA.

Emory Vaccine Center, Emory University, Atlanta, GA 30329, USA ; Division of Infectious Diseases, Department of Medicine, Emory University School of Medicine, Emory University, Atlanta, GA 30329, USA.

出版信息

J Immunol Res. 2015;2015:747543. doi: 10.1155/2015/747543. Epub 2015 Jul 14.

DOI:10.1155/2015/747543
PMID:26258152
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4516846/
Abstract

Tuberculosis (TB) remains a serious global public health problem that results in up to 2 million deaths each year. TB is caused by the human pathogen, Mycobacterium tuberculosis (Mtb), which infects primarily innate immune cells patrolling the lung. Innate immune cells serve as barometers of the immune response against Mtb infection by determining the inflammatory milieu in the lungs and promoting the generation of adaptive immune responses. However, innate immune cells are also potential niches for bacterial replication and are readily manipulated by Mtb. Our understanding of the early interactions between Mtb and innate immune cells is limited, especially in the context of human infection. This review will focus on Mtb interactions with human macrophages, dendritic cells, neutrophils, and NK cells and detail evidence that Mtb modulation of these cells negatively impacts Mtb-specific immune responses. Furthermore, this review will emphasize important innate immune pathways uncovered through human immunogenetic studies. Insights into the human innate immune response to Mtb infection are necessary for providing a rational basis for the augmentation of immune responses against Mtb infection, especially with respect to the generation of effective anti-TB immunotherapeutics and vaccines.

摘要

结核病(TB)仍然是一个严重的全球公共卫生问题,每年导致多达 200 万人死亡。结核病是由人类病原体结核分枝杆菌(Mtb)引起的,主要感染肺部巡逻的先天免疫细胞。先天免疫细胞通过确定肺部的炎症环境并促进适应性免疫反应的产生,充当针对 Mtb 感染的免疫反应的晴雨表。然而,先天免疫细胞也是细菌复制的潜在小生境,并且很容易被 Mtb 操纵。我们对 Mtb 与先天免疫细胞之间早期相互作用的理解是有限的,特别是在人类感染的情况下。本综述将重点介绍 Mtb 与人类巨噬细胞、树突状细胞、中性粒细胞和 NK 细胞的相互作用,并详细说明 Mtb 对这些细胞的调节如何对 Mtb 特异性免疫反应产生负面影响。此外,本综述将强调通过人类免疫遗传学研究揭示的重要先天免疫途径。深入了解人类对 Mtb 感染的先天免疫反应对于增强针对 Mtb 感染的免疫反应提供合理的基础是必要的,特别是在生成有效的抗结核免疫治疗和疫苗方面。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/137d/4516846/19d06ba849f2/JIR2015-747543.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/137d/4516846/47840010e3dd/JIR2015-747543.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/137d/4516846/5fde44552be5/JIR2015-747543.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/137d/4516846/36e8fed7124a/JIR2015-747543.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/137d/4516846/19d06ba849f2/JIR2015-747543.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/137d/4516846/47840010e3dd/JIR2015-747543.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/137d/4516846/5fde44552be5/JIR2015-747543.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/137d/4516846/36e8fed7124a/JIR2015-747543.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/137d/4516846/19d06ba849f2/JIR2015-747543.004.jpg

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本文引用的文献

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Mycobacterium tuberculosis 19-kDa lipoprotein induces Toll-like receptor 2-dependent peroxisome proliferator-activated receptor γ expression and promotes inflammatory responses in human macrophages.结核分枝杆菌19-kDa脂蛋白诱导Toll样受体2依赖性过氧化物酶体增殖物激活受体γ表达并促进人巨噬细胞中的炎症反应。
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结核分枝杆菌 Rv1048c 影响重组耻垢分枝杆菌的生物学特性。
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