IL28B Polymorphism Does Not Determine Outcomes of Hepatitis B Virus or HIV Infection

被引:99
作者
Martin, Maureen P. [2 ]
Qi, Ying [2 ]
Goedert, James J. [3 ]
Hussain, Shehnaz K. [5 ]
Kirk, Gregory D. [1 ]
Hoots, W. Keith [4 ]
Buchbinder, Susan [6 ]
Carrington, Mary [2 ]
Thio, Chloe L. [1 ]
机构
[1] Johns Hopkins Univ, Baltimore, MD 21205 USA
[2] NCI, Canc & Inflammat Program, Expt Immunol Lab, SAIC Frederick, Frederick, MD 21701 USA
[3] NCI, Infect & Immunoepidemiol Branch, Div Canc Epidemiol & Genet, Rockville, MD USA
[4] NHLBI, Div Blood Dis & Resources, Bethesda, MD 20892 USA
[5] Univ Calif Los Angeles, Los Angeles, CA USA
[6] Univ Calif San Francisco, San Francisco, CA 94143 USA
基金
美国国家卫生研究院;
关键词
C VIRUS; INTERFERON-LAMBDA; GENETIC-VARIATION; REPLICATION; CLEARANCE; CELLS; MICE;
D O I
10.1086/657146
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
An IL28B haplotype strongly determines the outcome of natural and interferon-alpha treated hepatitis C virus (HCV) infection. To assess whether the polymorphism marking the haplotype (rs12979860) also affects other interferon-alpha responsive chronic viral illnesses, namely hepatitis B virus (HBV) and human immunodeficiency virus (HIV) type 1 infections, we genotyped 226 individuals with HBV persistence, 384 with HBV recovery, and 2548 with or at high risk for HIV infection. The C/C genotype of rs12979860 was not associated with HBV recovery (odds ratio, 0.99), resistance to HIV infection (odds ratio, 0.97), or HIV disease progression (P>1.05). This IL28B single-nucleotide polymorphism affects the immune response to HCV but not to HBV or HIV.
引用
收藏
页码:1749 / 1753
页数:5
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