Department of Microbiology, Chungnam National University School of Medicine, Jungku, Daejeon, Korea.
Cell Microbiol. 2010 Aug;12(8):1026-35. doi: 10.1111/j.1462-5822.2010.01491.x. Epub 2010 Jun 14.
Autophagy is an ancient mechanism of protein degradation and a novel antimicrobial strategy. With respect to host defences against mycobacteria, autophagy plays a crucial role in antimycobacterial resistance, and contributes to immune surveillance of intracellular pathogens and vaccine efficacy. Vitamin D3 contributes to host immune responses against Mycobacterium tuberculosis through LL-37/hCAP-18, which is the only cathelicidin identified to date in humans. In this review, we discuss recent advances in our understanding of host immune strategies against mycobacteria, including vitamin D-mediated innate immunity and autophagy activation. This review also addresses our current understanding regarding the autophagy connection to principal innate machinery, such as ubiquitin- or inflammasome-involved pathways. Integrated dialog between autophagy and innate immunity may contribute to adequate host immune defences against mycobacterial infection.
自噬是一种古老的蛋白质降解机制,也是一种新的抗菌策略。就宿主对分枝杆菌的防御而言,自噬在抗分枝杆菌耐药性方面起着至关重要的作用,并有助于对细胞内病原体的免疫监视和疫苗效力。维生素 D3 通过 LL-37/hCAP-18 促进宿主对结核分枝杆菌的免疫反应,LL-37/hCAP-18 是迄今为止在人类中鉴定出的唯一一种抗菌肽。在这篇综述中,我们讨论了宿主对分枝杆菌免疫策略的最新进展,包括维生素 D 介导的先天免疫和自噬激活。本文还讨论了我们目前对自噬与先天免疫主要机制(如泛素或炎性小体相关途径)之间联系的理解。自噬和先天免疫之间的综合对话可能有助于宿主对分枝杆菌感染产生适当的免疫防御。