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Clin Diagn Lab Immunol. 1997 Sep;4(5):509-14. doi: 10.1128/cdli.4.5.509-514.1997.
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Specific interactions between rotavirus outer capsid proteins VP4 and VP7 determine expression of a cross-reactive, neutralizing VP4-specific epitope.轮状病毒外衣壳蛋白VP4和VP7之间的特异性相互作用决定了一种交叉反应性、中和性VP4特异性表位的表达。
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本文引用的文献

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Amino acids involved in distinguishing between monotypes of rotavirus G serotypes 2 and 4.参与区分轮状病毒G血清型2和4单型的氨基酸。
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2
Immunodominance of the VP4 neutralization protein of rotavirus in protective natural infections of young children.轮状病毒VP4中和蛋白在幼儿自然保护性感染中的免疫显性
J Virol. 1993 Jan;67(1):464-8. doi: 10.1128/JVI.67.1.464-468.1993.
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Immunodominant neutralizing antigens depend on the virus strain during a primary immune response in calves to bovine rotaviruses.在犊牛对牛轮状病毒的初次免疫应答过程中,免疫显性中和抗原取决于病毒株。
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Studies on the role of VP4 of G serotype 10 rotavirus (B223) in the induction of the heterologous immune response in calves.G10血清型10型轮状病毒(B223)VP4在犊牛异源免疫反应诱导中的作用研究。
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Evaluation of a bovine-human rotavirus reassortant vaccine in infants.婴儿中牛-人轮状病毒重组疫苗的评估。
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Genotypic diversity of reassortants between simian rotavirus SA11 and human rotaviruses having different antigenic specificities and RNA patterns.具有不同抗原特异性和RNA模式的猿猴轮状病毒SA11与人轮状病毒之间重配体的基因型多样性。
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Rotavirus antigenicity is affected by the genetic context and glycosylation of VP7.轮状病毒的抗原性受VP7的基因背景和糖基化作用影响。
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Efficient production of antigenic mosaic reassortants of rotavirus with the aid of anti-VP4 and anti-VP7 neutralizing monoclonal antibodies.借助抗VP4和抗VP7中和单克隆抗体高效生产轮状病毒的抗原嵌合重配体。
J Virol Methods. 1993 Sep;44(1):25-34. doi: 10.1016/0166-0934(93)90004-b.
10
A subviral particle binding domain on the rotavirus nonstructural glycoprotein NS28.轮状病毒非结构糖蛋白NS28上的亚病毒颗粒结合结构域。
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生产含有人类轮状病毒VP4和SA11 VP7的重配病毒,用于测量自然感染后的中和抗体。

Production of reassortant viruses containing human rotavirus VP4 and SA11 VP7 for measuring neutralizing antibody following natural infection.

作者信息

Gorrell R J, Bishop R F

机构信息

Department of Gastroenterology and Clinical Nutrition, Royal Children's Hospital, Parkville, Victoria, Australia.

出版信息

Clin Diagn Lab Immunol. 1997 Sep;4(5):509-14. doi: 10.1128/cdli.4.5.509-514.1997.

DOI:10.1128/cdli.4.5.509-514.1997
PMID:9302196
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC170582/
Abstract

The outer capsid proteins VP4 and VP7 of group A rotaviruses are both targets of neutralizing antibody produced following natural infection in humans. Of interest is the relative importance and immunodominance of each protein in the generation of a protective immune response. In order to measure neutralizing antibody responses to VP4 and VP7 separately, reassortants bearing VP4 of each of the major human rotavirus P types with VP7 of SA11 origin were successfully produced by neutralizing monoclonal antibody selection. The resulting reassortants, together with reassortants representing each of the major VP7 types, were antigenically characterized with serotype-specific neutralizing monoclonal antibodies and hyperimmune sera. The neutralization proteins of human rotavirus origin were found to be unaffected antigenically by reassortment. The abilities of these reassortants to discriminate between VP4 and VP7 immune responses were evaluated with postinfection sera collected from three patients infected with either a P1A[8],G1, a P1B[4],G2, or a P1A[8],G4 rotavirus strain. The reassortants were shown to be capable of separating the neutralizing antibody responses to VP4 and VP7, with each patient showing a different immune response with respect to VP4 or VP7 immunodominance. These reassortants can now be applied to analyses of individual immune responses to VP4 and VP7 proteins after primary rotavirus infections and reinfections in humans.

摘要

A组轮状病毒的外衣壳蛋白VP4和VP7都是人类自然感染后产生的中和抗体的靶标。有趣的是,每种蛋白在产生保护性免疫反应中的相对重要性和免疫显性。为了分别测量对VP4和VP7的中和抗体反应,通过中和单克隆抗体选择成功产生了携带每种主要人类轮状病毒P型的VP4与SA11来源的VP7的重配病毒。用血清型特异性中和单克隆抗体和超免疫血清对产生的重配病毒以及代表每种主要VP7类型的重配病毒进行了抗原特性分析。发现人类轮状病毒来源的中和蛋白在抗原性上不受重配的影响。用从三名分别感染P1A[8]、G1、P1B[4]、G2或P1A[8]、G4轮状病毒株的患者收集的感染后血清评估了这些重配病毒区分VP4和VP7免疫反应的能力。结果表明,重配病毒能够区分对VP4和VP7的中和抗体反应,每名患者在VP4或VP7免疫显性方面表现出不同的免疫反应。现在可以将这些重配病毒应用于分析人类初次轮状病毒感染和再次感染后对VP4和VP7蛋白的个体免疫反应。