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Decreased Frequency of the HLA-DRB1*11 Allele in Patients with Chronic Hepatitis C Virus Infection

机译:慢性丙型肝炎病毒感染患者HLA-DRB1 * 11等位基因频率降低

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摘要

A genetically determined resistance or susceptibility to chronic hepatitis C virus (HCV) infection may make an important contribution to the course of liver disease and may be linked to the human major histocompatibility complex (MHC). The aim of this study was to investigate the HLA class II genotype profile in chronic hepatitis C and to determine the HLA-hepatitis C association. The experimental population was composed of 49 unrelated chronic HCV patients (31 females, 18 males; mean age, 54.4 ± 1.7 years; range, 34 to 73 years). The control population consisted of 43 ethnically matched healthy donors. HLA-DR and -DQ alleles were studied for patients and controls by a PCR-sequence-specific-primer low-resolution method. Anti-HCV was investigated with enzyme-linked immunosorbent assay II, and HCV RNA was investigated with reverse transcriptase nested PCR. The HLA class II allele, DRB1*11, was found at reduced frequency in 49 patients with chronic hepatitis C (anti-HCV and HCV RNA positive) compared to that for controls (22.4 versus 51.0%; P < 0.01, odds ratio = 0.3, confidence interval = 0.1 to 0.7). No further HLA associations with chronic HCV infection were observed, and there was no correlation between the stage of disease and HLA. DRB1*11 was also found at reduced frequency in all HCV antibody-positive patients compared to controls (corrected P = not significant). DRB1*11 was associated with chronic HCV infection, and it is possible that HLA-DRB1*11 may have a protective feature in chronic HCV infection. In addition, DRB1*11 was associated with protection from HCV infection. These findings suggest that host HLA class II genotype is an important factor determining the outcome of infection with HCV.
机译:遗传确定的对慢性丙型肝炎病毒(HCV)感染的抗药性或易感性可能对肝病的进程做出重要贡献,并且可能与人类主要组织相容性复合物(MHC)相关。这项研究的目的是调查慢性丙型肝炎的HLA II类基因型概况,并确定HLA与丙型肝炎的关联。实验人群由49位无关的慢性HCV患者组成(女性31例,男性18例;平均年龄54.4±1.7岁;范围34到73岁)。对照人群由43个种族匹配的健康捐赠者组成。通过PCR序列特异性引物低分辨率方法研究了患者和对照的HLA-DR和-DQ等位基因。用酶联免疫吸附试验II研究了抗HCV,用逆转录酶巢式PCR研究了HCV RNA。在49例慢性丙型肝炎患者(抗HCV和HCV RNA阳性)中发现HLA II类等位基因DRB1 * 11的频率比对照组低(22.4%对51.0%; P <0.01,优势比= 0.3 ,置信区间= 0.1到0.7)。没有观察到进一步的HLA与慢性HCV感染的相关性,并且疾病的分期与HLA之间没有相关性。在所有HCV抗体阳性患者中,与对照组相比,DRB1 * 11的频率也降低了(校正后的P =不显着)。 DRB1 * 11与慢性HCV感染有关,HLA-DRB1 * 11可能在慢性HCV感染中具有保护作用。此外,DRB1 * 11与防止HCV感染相关。这些发现表明,宿主HLA II类基因型是决定HCV感染结果的重要因素。

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