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丙型肝炎病毒糖蛋白1和2抗体(抗-E1E2)与丙型肝炎病毒疾病的关联。

Association of antibodies to hepatitis C virus glycoproteins 1 and 2 (anti-E1E2) with HCV disease.

作者信息

Hamed M R B, Tarr A W, McClure C P, Ball J K, Hickling T P, Irving W L

机构信息

Division of Microbiology and Infectious Diseases, School of Molecular Medical Sciences, Institute of Infection, Immunity and Inflammation, University of Nottingham, Nottingham, UK.

出版信息

J Viral Hepat. 2008 May;15(5):339-45. doi: 10.1111/j.1365-2893.2007.00947.x. Epub 2008 Jan 22.

Abstract

Hepatitis C virus (HCV) causes acute and chronic liver diseases in humans. Its two envelope glycoproteins, E1 and E2, provide a target for host immune recognition. HCV genotypes are classified into six genetic groups. To study the role of anti-HCV E1 and E2 (anti-E1E2) in HCV disease, the correlation between antibody level and viral load, genotype, disease severity and response to treatment was investigated. The levels of antibodies to HCV glycoproteins E1 and E2 antibodies were evaluated in 230 sera of patients with chronic hepatitis C by enzyme-linked immunosorbent assay. The antigens used were recombinant HCV glycoproteins derived from genotype 1 (H77c) and genotype 3 (UKN3A1.28). Seroreactivity was greater when sera were tested against antigen derived from their homologous genotype than against heterologous antigen. Reactivity against UKN3A1.28 in sera from patients infected with genotype 3 was significantly higher than corresponding reactivity between patients infected with genotype 1 and H77c. The seroreactivity was inversely proportional to the viral load and to the degree of liver fibrosis. The pre-treatment level of anti-E1E2 was higher in sustained responders to combination therapy. These results demonstrate that seroreactivity against E1E2 depends upon the genotypic origin of the E1E2 antigens and the infecting genotype, and suggest a possible protective effect of anti-E1E2 against disease progression.

摘要

丙型肝炎病毒(HCV)可导致人类急性和慢性肝病。其两种包膜糖蛋白E1和E2是宿主免疫识别的靶点。HCV基因型分为六个遗传组。为研究抗HCV E1和E2(抗E1E2)在HCV疾病中的作用,研究了抗体水平与病毒载量、基因型、疾病严重程度及治疗反应之间的相关性。采用酶联免疫吸附试验评估了230例慢性丙型肝炎患者血清中HCV糖蛋白E1和E2抗体的水平。所用抗原为源自1型(H77c)和3型(UKN3A1.28)的重组HCV糖蛋白。血清与同源基因型来源的抗原反应时的血清反应性高于与异源抗原反应时的血清反应性。3型感染患者血清对UKN3A1.28的反应性显著高于1型感染患者与H77c之间的相应反应性。血清反应性与病毒载量和肝纤维化程度呈负相关。联合治疗持续应答者的抗E1E2治疗前水平较高。这些结果表明,针对E1E2的血清反应性取决于E1E2抗原的基因型来源和感染基因型,并提示抗E1E2对疾病进展可能具有保护作用。

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