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三种丙型肝炎病毒基因型的重组 Flag 标记 E1E2 糖蛋白具有生物学功能,并在小鼠中诱导交叉反应性中和抗体。

Recombinant Flag-tagged E1E2 glycoproteins from three hepatitis C virus genotypes are biologically functional and elicit cross-reactive neutralizing antibodies in mice.

机构信息

Laboratory of Virus Molecular Biology, Intercollegiate Faculty of Biotechnology of UG and MUG, University of Gdansk, 58 Abrahama str., 80-307 Gdansk, Poland.

MRC-University of Glasgow Centre for Virus Research, Sir Michael Stoker Building, Garscube Campus, 464 Bearsden Road, Glasgow G61 1QH, Scotland (UK).

出版信息

Virology. 2018 Jun;519:33-41. doi: 10.1016/j.virol.2018.03.026. Epub 2018 Apr 6.

Abstract

Hepatitis C virus (HCV) is a globally disseminated human pathogen for which no vaccine is currently available. HCV is highly diverse genetically and can be classified into 7 genotypes and multiple sub-types. Due to this antigenic variation, the induction of cross-reactive and at the same time neutralizing antibodies is a challenge in vaccine production. Here we report the analysis of immunogenicity of recombinant HCV envelope glycoproteins from genotypes 1a, 1b and 2a, with a Flag tag inserted in the hypervariable region 1 of E2. This modification did not affect protein expression or conformation or its capacity to bind the crucial virus entry factor, CD81. Importantly, in immunogenicity studies on mice, the purified E2-Flag mutants elicited high-titer, cross-reactive antibodies that were able to neutralize HCV infectious particles from two genotypes tested (1a and 2a). These findings indicate that E1E2-Flag envelope glycoproteins could be important immunogen candidates for vaccine aiming to induce broad HCV-neutralizing responses.

摘要

丙型肝炎病毒(HCV)是一种在全球传播的人类病原体,目前尚无可用的疫苗。HCV 在遗传上具有高度多样性,可分为 7 种基因型和多个亚型。由于这种抗原变异,诱导交叉反应性和同时具有中和活性的抗体是疫苗生产中的一个挑战。在这里,我们报告了对基因型 1a、1b 和 2a 的 HCV 包膜糖蛋白的免疫原性分析,在 E2 的高变区 1 中插入了 Flag 标签。这种修饰不影响蛋白表达或构象,也不影响其结合关键病毒进入因子 CD81 的能力。重要的是,在对小鼠的免疫原性研究中,纯化的 E2-Flag 突变体可诱导产生高滴度的交叉反应性抗体,能够中和两种测试基因型(1a 和 2a)的 HCV 感染性颗粒。这些发现表明,E1E2-Flag 包膜糖蛋白可能是诱导广泛 HCV 中和反应的疫苗的重要免疫原候选物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e066/5998380/84689975c9ed/gr1.jpg

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