Killer cell immunoglobulin like receptor gene association with tuberculosis

被引:20
作者
Pydi, Satya Sudheer
Sunder, Sharada Ramaseri
Venkatasubramanian, Sambasivan [2 ]
Kovvali, Srinivas [3 ]
Jonnalagada, Subbanna
Valluri, Vijaya Lakshmi [1 ]
机构
[1] LEPRA India, Immunol & Mol Biol Div, Blue Peter Publ Hlth & Res Ctr, Hyderabad 501301, Andhra Pradesh, India
[2] Univ Texas Hlth Sci Ctr Tyler, Tyler, TX USA
[3] Anthropol Survey India, So Reg Ctr, Mysore, Karnataka, India
关键词
KIR GENES; HLA-C; INTRACELLULAR PATHOGEN; RHEUMATOID-ARTHRITIS; INHIBITORY RECEPTORS; PSORIATIC-ARTHRITIS; DIVERSITY; DISEASE; SUSCEPTIBILITY; COMBINATIONS;
D O I
10.1016/j.humimm.2012.10.006
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
NK cells are vital components of innate immune system and are the first cells which come into picture mediating resistance against intracellular pathogens. NK cell cytotoxicity is modulated by a wide variety of cell surface receptors that recognize and respond towards infected cells. Activation of NK cells are controlled by both inhibitory and activating receptors, encoded by KIR genes and bind to HLA ligands. Not much is known about KIR genes and their influence on the pathogenesis with M. tuberculosis infection. Our study aimed at detecting the presence of 14 KIR genes, their distribution and their association with tuberculosis. Total 77 different genotype combinations were observed which belonged to B-haplotype. Fifteen genotypes were similar to those reported in other world populations while remaining 62 were unique to this study group. Inhibitory genes KIR3DL1, KIR2DL3 and activating genes KIR2DS1, KIR2DS5 conferred susceptibility towards TB either individually or in haplotype combinations. The complimentary MHC ligands need to be tested for the functional relevance of the associated genes. (C) 2012 American Society for Histocompatibility and Immunogenetics. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:85 / 92
页数:8
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