Freund's adjuvant, NOD2 and mycobacteria

被引:34
作者
Behr, Marcel A. [1 ,2 ]
Divangahi, Maziar [1 ,2 ,3 ]
机构
[1] McGill Univ, Ctr Hlth, Dept Med, Montreal, PQ H3G 1A4, Canada
[2] McGill Int TB Ctr, Montreal, PQ H3G 1A4, Canada
[3] McGill Univ, Meakins Christie Labs, Montreal, PQ H2X 2P2, Canada
关键词
TOLL-LIKE RECEPTORS; CROHNS-DISEASE; MURAMYL DIPEPTIDE; HUMAN MACROPHAGES; TUBERCULOSIS; SUSCEPTIBILITY; PEPTIDOGLYCAN; BACTERIAL; LEPROSY; PARATUBERCULOSIS;
D O I
10.1016/j.mib.2014.11.015
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Purpose: Mycobacterium tuberculosis contributed to the discovery of delayed-type hypersensitivity and cell-mediated immunity. However, the biochemical basis for the immunogenicity of the mycobacterial cell wall has until recently remained unknown. Recent findings: Nucleotide-binding oligomerization domain-containing protein 2 (NOD2) responds to bacterial peptidolycan-derived muramyl dipeptide (MDP). Whereas most bacteria produce N-acetyl MDP, nnycobacteria produce an unusual modified form of MDP, called N-glycolyl MDP. Disruption of N-glycolyl MDP synthesis in mycobacteria greatly diminishes the contribution of NOD2 to mycobacterial sensing. Additionally, N-glycolyl MDP is more potent and efficacious than N-acetyl MDP at inducing innate responses and T cell-mediated immunity. Summary: The sensitivity of NOD2 to the mycobacterial peptidoglycan may link the natural history of both innate and adaptive immunity to mycobacterial infection.
引用
收藏
页码:126 / 132
页数:7
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