| Literature DB >> 27363694 |
Nicholas Bowker1, Muneeb Salie1, Haiko Schurz1, Paul D van Helden1, Craig J Kinnear1, Eileen G Hoal1, Marlo Möller2.
Abstract
The mechanisms involved in interactions between Mycobacterium tuberculosis and host innate immune cells determine outcome. Antigen-presenting cells, including macrophages and dendritic cells, express many pattern recognition receptors to identify pathogen-associated molecular patterns, thereby initiating an immune response. A major mycobacterial virulence factor, trehalose-6',6-dimycolate, is recognised by the macrophage-inducible C-type lectin, Mincle, which leads to the activation of the Syk-Card9 signalling pathway in macrophages. Mincle is encoded by CLEC4E, and we investigated polymorphisms in this gene to assess its role in tuberculosis susceptibility. Four tagging single nucleotide polymorphisms (SNPs) (rs10841845, rs10841847, rs10841856 and rs4620776) were genotyped using TaqMan(®) SNP assays in 416 tuberculosis cases and 405 healthy controls. Logistic regression models were used for analysis. No association was detected with any of the SNPs analysed. This research highlights tuberculosis disease complexity where recognition proteins which specifically bind mycobacterial glycolipids cannot be conclusively associated with the disease in genetic studies.Entities:
Keywords: CLEC4E; Mincle; Mycobacterium tuberculosis; Polymorphism; Susceptibility
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Year: 2016 PMID: 27363694 DOI: 10.1007/s00408-016-9915-y
Source DB: PubMed Journal: Lung ISSN: 0341-2040 Impact factor: 2.584