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埃及丙型肝炎病毒感染结局的人类白细胞抗原 II-DRB1 等位基因:一项基于多中心家族的研究。

HLA Class II-DRB1 Alleles with Hepatitis C Virus Infection Outcome in Egypt: A Multicentre Family-based Study.

机构信息

Tropical Medicine & Hepatology, Mansoura Faculty Of Medicine, Mansoura University, Mansoura,Dakahlyia, Egypt.

Medical Biochemistry, Mansoura Faculty of Medicine, Mansoura University, Mansoura, Dakahlyia, Egypt.

出版信息

Ann Hepatol. 2019 Jan-Feb;18(1):68-77. doi: 10.5604/01.3001.0012.7864.

Abstract

INTRODUCTION AND AIM

Hepatitis C virus (HCV) infection is a global medical problem. HLA -DRB1 alleles have an important role in immune response against HCV. The aim of this study is to clarify the contribution of HLA -DRB1 alleles in HCV susceptibility in a multicentre family-based study.

MATERIAL AND METHODS

A total of 162 Egyptian families were recruited in this study with a total of 951 individuals (255 with chronic hepatitis C (CHC), 588 persons in the control group(-ve household contact to HCV) and 108 persons who spontaneously cleared the virus (SVC). All subjects were genotyped for HLA -DRB1 alleles by SSP-PCR and sequence based typing (SBT) methods.

RESULTS

The carriage of alleles 3:01:01 and 13:01:01 were highly significant in CHC when compared to that of control and SVC groups [OR of 3 family = 5.1289, P (Bonferroni correction ) = 0.0002 and 5.9847, P = 0.0001 and OR of 13 family = 4.6860, P = 0.0002 and OR = 6.5987, P = 0.0001 respectively]. While DRB1040501, DRB1040101, DRB17:01:01 and DRB1110101 alleles were more frequent in SVC group than CHC patients (OR = 0.4052, P = 0.03, OR: OR = 0.0916,P = 0.0006, OR = 0.1833,P = 0.0006 and OR = 0.4061, P = 0.0001 respectively).

CONCLUSIONS

It was concluded that among the Egyptian families, HLA-DRB1030101, and DRB1130101 alleles associated with the risk of progression to CHC infection, while DRB1040101, DRB1040501, DRB17:01:01and DRB1110101 act as protective alleles against HCV infection.

摘要

简介与目的

丙型肝炎病毒(HCV)感染是一个全球性的医学问题。人类白细胞抗原-DRB1 等位基因在 HCV 免疫反应中起着重要作用。本研究的目的是在一项多中心基于家庭的研究中阐明 HLA-DRB1 等位基因在 HCV 易感性中的作用。

材料与方法

本研究共招募了 162 个埃及家庭,共 951 人(255 例慢性丙型肝炎(CHC)患者、588 例对照组(HCV 家庭阴性接触者)和 108 例自发清除病毒(SVC)者)。所有受试者均采用序列特异性引物聚合酶链反应(SSP-PCR)和序列基序分型(SBT)方法进行 HLA-DRB1 等位基因分型。

结果

与对照组和 SVC 组相比,CHC 患者携带等位基因 3:01:01 和 13:01:01 的比例显著升高[3 家族 OR = 5.1289,P(Bonferroni 校正)= 0.0002;13 家族 OR = 5.9847,P = 0.0001]。而 DRB1040501、DRB1040101、DRB17:01:01 和 DRB1110101 等位基因在 SVC 组中比 CHC 患者更常见(OR = 0.4052,P = 0.03;OR = 0.0916,P = 0.0006;OR = 0.1833,P = 0.0006;OR = 0.4061,P = 0.0001)。

结论

在埃及家庭中,HLA-DRB1030101 和 DRB1130101 等位基因与 CHC 感染进展的风险相关,而 DRB1040101、DRB1040501、DRB17:01:01 和 DRB1110101 等位基因则作为 HCV 感染的保护等位基因。

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