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代表丙型肝炎病毒核心蛋白和包膜蛋白选定片段的合成肽与一组丙型肝炎病毒血清阳性的人血浆的反应性。

Reactivity of synthetic peptides representing selected sections of hepatitis C virus core and envelope proteins with a panel of hepatitis C virus-seropositive human plasma.

作者信息

Jackson P, Petrik J, Alexander G J, Pearson G, Allain J P

机构信息

Department of Haematology, University of Cambridge, England.

出版信息

J Med Virol. 1997 Jan;51(1):67-79. doi: 10.1002/(sici)1096-9071(199701)51:1<67::aid-jmv11>3.0.co;2-1.

DOI:10.1002/(sici)1096-9071(199701)51:1<67::aid-jmv11>3.0.co;2-1
PMID:8986952
Abstract

A series of 54 synthetic peptides, 15-20 residues long, that represented selected parts of the structural proteins of hepatitis C virus (HCV) were tested for immunoreactivity with a panel of 45 plasma samples from potential blood donors who were known to be seropositive for anti-HCV. Most of the ten peptides that represented the core protein showed reactivity with most of the panel samples. All except one of the 20 peptides that represented non-hypervariable regions of envelope proteins E1 and E2 showed little or no reactivity. In contrast, 18 of the the 24 peptides that represented variants of the hypervariable region 1 of the E2 protein reacted with at least one panel sample. Notably, 40% of the panel samples cross-reacted with two or more different peptides sequences some of which differed by more than 50%. Two panel samples each cross-reacted with seven different peptide sequences. The results suggest a broad anti-hypervariable region antibody specificity in many anti-HCV-seropositive samples and possible limits on the mutability of hypervariable region sequences. The work contributes to understanding the immunogenicity and persistence of HCV.

摘要

对一系列54种合成肽进行了测试,这些肽长度为15 - 20个残基,代表丙型肝炎病毒(HCV)结构蛋白的选定部分,用一组来自已知抗HCV血清阳性的潜在献血者的45份血浆样本检测其免疫反应性。代表核心蛋白的十种肽中的大多数与大多数样本呈反应性。代表包膜蛋白E1和E2非高变区的20种肽中,除一种外,其余的几乎没有或没有反应性。相比之下,代表E2蛋白高变区1变体的24种肽中有18种与至少一份样本发生反应。值得注意的是,40%的样本与两种或更多不同的肽序列发生交叉反应,其中一些肽序列的差异超过50%。两份样本各自与七种不同的肽序列发生交叉反应。结果表明,许多抗HCV血清阳性样本中存在广泛的抗高变区抗体特异性,并且高变区序列的可变性可能存在限制。这项工作有助于理解HCV的免疫原性和持续性。

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