MICA and recovery from hepatitis C virus and hepatitis B virus infections

被引:0
|
作者
P S Karacki
X Gao
C L Thio
D L Thomas
J J Goedert
D Vlahov
R A Kaslow
S Strathdee
M W Hilgartner
S J O'Brien
M Carrington
机构
[1] Johns Hopkins Medical Institutions,Department of Medicine
[2] Intramural Research Support Program,Department of Epidemiology
[3] Basic Research Program,Department of Epidemiology
[4] SAIC Frederick,Department of Pediatrics
[5] Johns Hopkins Medical Institutions,undefined
[6] Viral Epidemiology Branch,undefined
[7] National Cancer Institute,undefined
[8] New York Academy of Medicine,undefined
[9] University of Alabama,undefined
[10] New York Presbyterian Hospital-Cornell Medical Center,undefined
[11] Laboratory of Genomic Diversity,undefined
[12] National Cancer Institute,undefined
来源
Genes & Immunity | 2004年 / 5卷
关键词
HCV; HBV; MICA; genetics; viral persistence; pathogenesis;
D O I
暂无
中图分类号
学科分类号
摘要
The polymorphic MHC class I chain-related A (MICA) gene encodes a ligand that has different binding affinities for the NKG2D activating receptor of CD8+ T cells and natural killer (NK) cells. We hypothesized that MICA heterogeneity would affect recovery from hepatitis C virus (HCV) and hepatitis B virus (HBV) infections. To test the hypothesis, we initially typed known MICA polymorphisms for 228 persons who cleared HCV infection and 442 persons with persistent hepatitis C matched on other factors affecting viral persistence. Although MICA*015 was detected more than two-fold more often in persons with viral clearance (odds ratio 0.36, 95% confidence interval=0.19, 0.80), it occurred in fewer than 5% of the study population. In a similar analysis of 442 persons with chronic hepatitis B and 768 matched controls who recovered, MICA*015 was detected in 2.0% of persons with chronic hepatitis B and only 0.9% of controls. No significant associations were detected with other MICA polymorphisms. While further investigation may reveal a structural basis of the MICA*015 associations, these data provide little support for the hypothesis that differential distribution of MICA alleles substantially affects recovery from HCV and HBV infections.
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页码:261 / 266
页数:5
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