Regulatory polymorphisms in the interleukin-18 promoter are associated with hepatitis C virus clearance

被引:45
|
作者
An, Ping [1 ]
Thio, Chloe L. [2 ]
Kirk, Gregory D. [3 ]
Donfield, Sharyne [5 ]
Goedert, James J. [4 ]
Winkler, Cheryl A. [1 ]
机构
[1] Sci Applicat Int Corp, Lab Genom Divers, Frederick, MD USA
[2] Johns Hopkins Med Inst, Dept Med, Baltimore, MD 21205 USA
[3] Johns Hopkins Sch Publ Hlth, Dept Epidemiol, Baltimore, MD USA
[4] NCI, Viral Epidemiol Branch, Div Canc Epidemiol & Genet, Bethesda, MD 20892 USA
[5] Rho Inc, Chapel Hill, NC USA
来源
JOURNAL OF INFECTIOUS DISEASES | 2008年 / 198卷 / 08期
关键词
D O I
10.1086/592047
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The immune response is critical in determining the outcome of hepatitis C virus (HCV) infection. Interleukin (IL)-18 is a pivotal mediator of the Th1/Th2-driven immune response. Two IL-18 promoter polymorphisms (-607C/A and -137G/C) and their haplotypes were known to affect IL-18 expression. We examined the role played by these polymorphisms in determining HCV clearance or persistence. Genotyping was performed among African American injection drug users with HCV clearance (n = 91) or HCV persistence ( n = 182) and among European Americans with hemophilia who were mainly infected through plasma transfusion. Among injection drug users, IL18 -607A (odds ratio [OR], 3.68 [95% confidence interval{CI}, 1.85-7.34]) and IL18 -137C ( OR, 2.33 [95% CI, 1.24-4.36]) were significantly associated with HCV clearance. A haplotype carrying -607A and -137C (OR, 4.53 [95% CI, 1.77-11.6]) was also strongly associated with viral clearance. No association was found among those with hemophilia. These results suggest that IL-18 promoter polymorphism may affect the outcome of HCV infection in certain groups.
引用
收藏
页码:1159 / 1165
页数:7
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