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Epistatic Interaction between Genetic Variants in Susceptibility Gene ETS1 Correlates with IL-17 Levels in SLE Patients.

Authors :
Zhang, Jing
Zhang, Yan
Zhang, Lu
Yang, Jing
Ying, Dingge
Zeng, Shuai
Lee, Tsz Leung
Lau, Chak Sing
Chan, Tak Mao
Leung, Alexander Moon Ho
Mok, Chi Chiu
Wong, Sik Nin
Lee, Ka Wing
Ho, Marco Hok Kung
Lee, Pamela Pui Wah
Hon‐Yin Chung, Brian
Chong, Chun Yin
Wong, Raymond Woon Sing
Mok, Mo Yin
Wong, Wilfred Hing Sang
Source :
Annals of Human Genetics; Jul2013, Vol. 77 Issue 4, p344-350, 7p
Publication Year :
2013

Abstract

T-helper cells that produce IL-17 (Th17 cells) are a subset of CD4<superscript>+</superscript> T-cells with pathological roles in autoimmune diseases including systemic lupus erythematosus (SLE), and ETS1 is a negative regulator of Thl7 cell differentiation. Our previous work on genome-wide association study (GWAS) identified two variants in the ETS1 gene (rs10893872 and rsl 128334) as being associated with SLE. However, like many other risk alleles for complex diseases, little is known on how these genetic variants might affect disease pathogenesis. In this study, we examined serum IL-17 levels from 283 SLE cases and observed a significant correlation between risk variants in ETS1 and serum IL-17 concentration in patients, which suggests a potential mechanistic link between these variants and the disease. Furthermore, we found that the two variants act synergistically in influencing IL-17 production, with evidence of significant genetic interaction between them as well as higher correlation between the haplotype formed by the risk alleles and IL-17 level in patient serum. In addition, the correlation between ETS1 variants and IL-17 level seems to be more significant in SLE patients manifesting renal involvement, dsDNA autoantibody production or early-onset. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00034800
Volume :
77
Issue :
4
Database :
Complementary Index
Journal :
Annals of Human Genetics
Publication Type :
Academic Journal
Accession number :
88835905
Full Text :
https://doi.org/10.1111/ahg.12018