古巴比伦省乙型肝炎病毒合并β -地中海贫血患者某些免疫指标的测定

Estabraq Hasan Alwan, Abd Alnabe J Almamorri, Naeem Rahman Aljubore
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引用次数: 0

摘要

丙型肝炎是世界范围内严重的公共卫生问题。地中海贫血患者全程依赖输血,病毒感染的风险很高。本研究旨在估计多重地中海贫血人群中丙型肝炎感染的患病率和不同的临床参数(HLA)。本研究纳入了66例感染性并发症-地中海贫血患者,分析了从伊拉克巴比伦省Babel妇幼医院遗传血液学中心采集的感染HCV、血清铁蛋白、pcv和脾切除术的样本。乙型肝炎病毒和丙型肝炎病毒的总患病率分别为3%和55%;在10-20岁以上的丙型肝炎患者中,100%的人感染丙型肝炎,并且有不同的HLA分子出现,HLA分子分为HLAⅱ类(HLA- dr)和HLAⅰ类(HLAG)。在本研究中,我们综述了HLA- g和HLA- dr基因的分子和几个参数在病毒性肝炎中的作用,肝炎的研究表明,甚至人类白细胞抗原也参与了该病的发病机制。hla分类结合基因调控元件的研究可能有助于了解遗传背景对疾病易感性的影响。关键词:肝炎及既往地中海贫血患者HLA检测
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Estimation of some immunological markers for patients with Hepatitis C and B viruses with β -thalassemia major in Babylon province
Hepatitis C, B is a severe public health problem worldwide. Thalassemia patients depend on blood transfusions throughout and are at high risk of viral infections. This study aimed to estimate the prevalence of hepatitis C infection and different clinical parameters of (HLA) in the multiplex thalassemia population. In this study, 66 patients with infectious complications beta-thalassemia were enrolled, and samples collected from the Genetic Hematology Center at Babel Women and Children Hospital in Babylon Governorate / Iraq infected with HCV, serum ferritin, PCV and splenectomy were analyzed. The overall prevalence of hepatitis B virus and HCV was 3% and 55%, respectively; 100% of patients over 10-20 years of age had hepatitis C infection, and some episodes were presented by different HLA molecules, by molecule HLA from HLA class II (HLA-DR) and HLA class I (HLAG), In this study, we review the role of the molecule and several parameters along the HLA-G and HLA-DR gene in viral hepatitis, studies of hepatitis suggest that even Human leukocyte antigen contributes to the pathogenesis of the disease. HLA classification combined with the study of the regulatory elements of genes may help understand the influence of genetic background on susceptibility to disease. Keywords: Detection of some immunological markers (HLA) for hepatitis patients and those with a previous infection with thalassemia
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