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人轮状病毒感染中针对单个病毒多肽的血清抗体反应。

Serum antibody responses to individual viral polypeptides in human rotavirus infections.

作者信息

Svensson L, Sheshberadaran H, Vene S, Norrby E, Grandien M, Wadell G

出版信息

J Gen Virol. 1987 Mar;68 ( Pt 3):643-51. doi: 10.1099/0022-1317-68-3-643.

Abstract

A radioimmunoprecipitation assay (RIPA) was used to study the serum antibody responses to individual polypeptides that developed after infection with viruses from human rotavirus subgroups I and II. Paired sera from eight children (1 to 8.5 years of age) were used in the study. Although all of the eight acute sera were negative by the complement fixation test, four of them were positive by RIPA, indicating a previous infection by rotavirus. A significant difference in the number of polypeptides immunoprecipitated was seen among the convalescent sera. The number of polypeptides immunoprecipitated was found to be related to previous infection experience. At most, ten different polypeptides were immunoprecipitated: seven structural polypeptides VP1 to VP7 and three non-structural polypeptides, NS1, NS2 and NS3. No sera immunoprecipitated VP8 or VP9. Acute sera positive by RIPA immunoprecipitated up to five polypeptides, VP1, VP2, VP3, VP4 and VP6. One of the non-structural proteins (NS2) was found to be particularly immunogenic, since antibodies to this polypeptide were detected in several convalescent sera. Among the structural proteins VP2 and VP6 were found to be the two immunodominant polypeptides which were recognized by all convalescent sera. Only three convalescent sera immunoprecipitated VP7, the major type-specific antigen responsible for inducing neutralizing antibodies. Three of four originally seronegative children with no reactivity in the convalescent sera to VP7 developed neutralizing antibodies to a single serotype. One child developed antibodies to two serotypes.

摘要

采用放射免疫沉淀试验(RIPA)研究感染人轮状病毒I和II亚组病毒后产生的针对单个多肽的血清抗体反应。研究使用了8名儿童(1至8.5岁)的配对血清。尽管所有8份急性期血清通过补体结合试验均为阴性,但其中4份通过RIPA呈阳性,表明先前感染过轮状病毒。恢复期血清中免疫沉淀的多肽数量存在显著差异。发现免疫沉淀的多肽数量与先前的感染经历有关。最多可免疫沉淀出10种不同的多肽:7种结构多肽VP1至VP7以及3种非结构多肽NS1、NS2和NS3。没有血清能免疫沉淀VP8或VP9。RIPA呈阳性的急性期血清最多可免疫沉淀5种多肽,即VP1、VP2、VP3、VP4和VP6。发现其中一种非结构蛋白(NS蛋白)具有特别强的免疫原性,因为在几份恢复期血清中检测到了针对该多肽的抗体。在结构蛋白中,发现VP2和VP6是所有恢复期血清都能识别的两种免疫显性多肽。只有3份恢复期血清免疫沉淀出VP7,VP7是负责诱导中和抗体的主要型特异性抗原。4名最初血清学阴性且恢复期血清对VP7无反应的儿童中,有3名产生了针对单一血清型的中和抗体。1名儿童产生了针对两种血清型的抗体。

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