The molecular basis and downstream immune consequences of mycobacteria-host cell interactions

被引:5
|
作者
Daher, Wassim [1 ,2 ]
Pichler, Virginia [1 ,3 ]
Karam, Jona [1 ]
Neyrolles, Olivier [4 ]
Kremer, Laurent [1 ,2 ]
机构
[1] Univ Montpellier, Inst Rech Infectiol Montpellier IRIM, CNRS, UMR 9004, 1919 Route Mende, F-34293 Montpellier, France
[2] INSERM, IRIM, 1919 Route Mende, Montpellier, France
[3] Univ British Columbia, Dept Microbiol & Immunol, Vancouver, BC V6T 1Z3, Canada
[4] Univ Toulouse, Inst Pharmacol & Biol Struct, IPBS, CNRS,UPS, 205 Route Narbonne, Toulouse, France
关键词
adhesin; receptor; host-pathogen interaction; internalization; Mycobacterium; macrophage; C-TYPE LECTIN; FIBRONECTIN ATTACHMENT PROTEIN; HEPARIN-BINDING HEMAGGLUTININ; TOLL-LIKE RECEPTORS; MANNOSE-CAPPED LIPOARABINOMANNAN; PATTERN-RECOGNITION RECEPTORS; HUMAN DENDRITIC CELLS; DC-SIGN; TUBERCULOSIS INFECTION; EPITHELIAL-CELLS;
D O I
10.1093/femsre/fuad009
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
This review summarizes the complexity of the interactions between mycobacterial ligands and host receptors during infection and pathogenesis. Pathogenic mycobacteria gain entry to their hosts by inhalation or ingestion where they adhere to different cell types and are subsequently internalized by professional phagocytic cells, such as macrophages or dendritic cells. Multiple pathogen-associated molecular patterns present on the mycobacterial surface are recognized by and interact with a diverse panel of phagocytic pattern recognition receptors, representing the first step of the infection process. This review summarizes the current knowledge on the numerous host cell receptors and their associated mycobacterial ligands or adhesins. It further discusses the downstream molecular and cellular events resulting from the engagement of the various receptor-mediated pathways, leading to either intracellular survival of mycobacteria or to activation of host immune defenses. The content presented herein on adhesins and host receptors may serve as a resource for those developing novel therapeutic approaches, e.g. in the design of antiadhesin molecules to prevent bacterial attachment and infection. The collection of mycobacterial surface molecules highlighted in this review may also provide potential new therapeutic targets, diagnostic markers, or vaccine candidates to combat these notoriously challenging and persistent pathogens.
引用
收藏
页数:25
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