Pathogenesis of HIV-1 and Mycobacterium tuberculosis co-infection

被引:241
|
作者
Bell, Lucy C. K. [1 ]
Noursadeghi, Mahdad [1 ]
机构
[1] UCL, Div Infect & Immun, Cruciform Bldg, London WC1E 6BT, England
基金
英国医学研究理事会; 英国惠康基金;
关键词
HUMAN-IMMUNODEFICIENCY-VIRUS; TUMOR-NECROSIS-FACTOR; RECONSTITUTION INFLAMMATORY SYNDROME; TOLL-LIKE RECEPTOR; INNATE IMMUNE-RESPONSES; LONG TERMINAL REPEAT; CD4; T-CELLS; FACTOR-ALPHA; ALVEOLAR MACROPHAGES; HIV-1-INFECTED MACROPHAGES;
D O I
10.1038/nrmicro.2017.128
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Co-infection with Mycobacterium tuberculosis is the leading cause of death in individuals infected with HIV-1. It has long been known that HIV-1 infection alters the course of M. tuberculosis infection and substantially increases the risk of active tuberculosis ( TB). It has also become clear that TB increases levels of HIV-1 replication, propagation and genetic diversity. Therefore, co-infection provides reciprocal advantages to both pathogens. In this Review, we describe the epidemiological associations between the two pathogens, selected interactions of each pathogen with the host and our current understanding of how they affect the pathogenesis of TB and HIV-1/AIDS in individuals with co-infections. We evaluate the mechanisms and consequences of HIV-1 depletion of T cells on immune responses to M. tuberculosis. We also discuss the effect of HIV-1 infection on the control of M. tuberculosis by macrophages through phagocytosis, autophagy and cell death, and we propose models by which dysregulated inflammatory responses drive the pathogenesis of TB and HIV-1/AIDS.
引用
收藏
页码:80 / 90
页数:11
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