Yoon Seung Kew, Han Joon Yeol, Pyo Chul-Woo, Yang Jin Mo, Jang Jeong Won, Kim Chang Wook, Chang U Im, Bae Si Hyun, Choi Jong Young, Chung Kyu Won, Sun Hee Sik, Choi Hee Baeg, Kim Tai-Gyu
Department of Internal Medicine, WHO Collaborating Center for Reference and Research on Viral Hepatitis, Seoul, Korea.
Liver Int. 2005 Dec;25(6):1122-7. doi: 10.1111/j.1478-3231.2005.01105.x.
BACKGROUND/AIM: Recent data have shown that the clinical outcome of hepatitis C virus (HCV) infection may be influenced by the host genetic factor. The aim of this study was to investigate whether particular human leukocytes antigen (HLA) molecules are associated with the susceptibility to HCV infection in the Korean population.
One hundred and thirty-seven patients with chronic HCV infection and 206 normal individuals were examined for HLA class I and II molecules.
In class I antigens, the frequencies of HLA-A3 (relative risk (RR)=3.5, P<0.04), HLA-B35 (RR=2.0, P<0.03), and HLA-B46 (RR=2.5, P<0.02) significantly increased in chronic HCV carriers compared with the controls. The frequencies of DRB10803, DQB10601 and DQB10604 were significantly higher in chronic HCV carriers than in controls (RR=2.5, P<0.005; RR=1.8, P<0.05; RR=1.9, P<0.04, respectively). On the other hand, the frequencies of DRB10301, DQA10501 and DQB10201 were significantly lower in chronic HCV carriers than in normal controls (RR=0.2, P<0.03; RR=0.4, P<0.004; RR=0.5, P<0.02, respectively). The haplotype DRB10803-DQB10601 significantly increased (RR=2.5, P<0.02) while the DQA10501-DQB10201 significantly decreased (RR=0.2, P<0.03) in chronic HCV carriers compared with normal controls. In stratification analysis to investigate the interrelationships among the associated alleles, DRB10803 and DQB10601 were associated with HLA-B46, particularly in patients with chronic HCV carriers.
These results suggest that particular HLA alleles may have an influence on chronic HCV infection as a host genetic factor in the Korean population.
背景/目的:近期数据表明,丙型肝炎病毒(HCV)感染的临床结局可能受宿主遗传因素影响。本研究旨在调查特定人类白细胞抗原(HLA)分子是否与韩国人群对HCV感染的易感性相关。
对137例慢性HCV感染患者和206名正常个体进行了HLA I类和II类分子检测。
在I类抗原中,与对照组相比,慢性HCV携带者中HLA - A3(相对风险(RR)=3.5,P<0.04)、HLA - B35(RR=2.0,P<0.03)和HLA - B46(RR=2.5,P<0.02)的频率显著增加。慢性HCV携带者中DRB10803、DQB10601和DQB10604的频率显著高于对照组(RR分别为2.5,P<0.005;RR=1.8,P<0.05;RR=1.9,P<0.04)。另一方面,慢性HCV携带者中DRB10301、DQA10501和DQB10201的频率显著低于正常对照组(RR分别为0.2,P<0.03;RR=0.4,P<0.004;RR=0.5,P<0.02)。与正常对照组相比,慢性HCV携带者中DRB10803 - DQB10601单倍型显著增加(RR=2.5,P<0.02),而DQA10501 - DQB10201单倍型显著减少(RR=0.2,P<0.03)。在分层分析以研究相关等位基因之间的相互关系时,DRB10803和DQB10601与HLA - B46相关,特别是在慢性HCV携带者患者中。
这些结果表明,特定的HLA等位基因作为宿主遗传因素可能对韩国人群的慢性HCV感染有影响。