4.5 Article

An association study of TOLL and CARD with leprosy susceptibility in Chinese population

期刊

HUMAN MOLECULAR GENETICS
卷 22, 期 21, 页码 4430-4437

出版社

OXFORD UNIV PRESS
DOI: 10.1093/hmg/ddt286

关键词

-

资金

  1. National Natural Science Foundation of China [81071288, 81072391, 81101187]
  2. National 973 program [2011CB512105]
  3. Project of Taishan scholar
  4. Project of Medical leading scholar of Shandong Province
  5. Natural Science Foundation of Shandong Province [ZR2011HQ003]
  6. Ministry of Education of China [IRT-1046]
  7. Agency for Science, Technology and Research (A*STAR) of Singapore
  8. Singapore International Graduate Award
  9. special foundation of Shandong Medical Leading Scholar [20121212]

向作者/读者索取更多资源

Previous genome-wide association studies (GWASs) identified multiple susceptibility loci that have highlighted the important role of TLR (Toll-like receptor) and CARD (caspase recruitment domain) genes in leprosy. A large three-stage candidate gene-based association study of 30 TLR and 47 CARD genes was performed in the leprosy samples of Chinese Han. Of 4363 SNPs investigated, eight SNPs showed suggestive association (P 0.01) in our previously published GWAS datasets (Stage 1). Of the eight SNPs, rs2735591 and rs4889841 showed significant association (P 0.001) in an independent series of 1504 cases and 1502 controls (Stage 2), but only rs2735591 (next to BCL10) showed significant association in the second independent series of 938 cases and 5827 controls (Stage 3). Rs2735591 showed consistent association across the three stages (P 0.05 for heterogeneity test), significant association in the combined validation samples (P-corrected 5.54 10(4) after correction for 4363 SNPs tested) and genome-wide significance in the whole GWAS and validation samples (P 1.03 10(9), OR 1.24). In addition, we demonstrated the lower expression of BCL10 in leprosy lesions than normal skins and a significant gene connection between BCL10 and the eight previously identified leprosy loci that are associated with NFB, a major regulator of downstream inflammatory responses, which provides further biological evidence for the association. We have discovered a novel susceptibility locus on 1p22, which implicates BCL10 as a new susceptibility gene for leprosy. Our finding highlights the important role of both innate and adaptive immune responses in leprosy.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据