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Antigenic drift in influenza A viruses. I. Selection and characterization of antigenic variants of A/PR/8/34 [HON1] influenza virus with monoclonal antibodies

机译:甲型流感病毒的抗原漂移。 I.用单克隆抗体对A / PR / 8/34 [HON1]流感病毒的抗原变体进行选择和表征

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摘要

Antigenic variants of A/PR/8/34 [HON1] influenza virus were selected after a single passage of the parent virus in embryonated chicken eggs in the presence of monoclonal antibodies to this virus. The monoclonal antibodies were produced by a hybridoma and were specific for an antigenic determinant on the HA molecule of the parent virus. Seven antigenic variants were analyzed with 95 monoclonal anti-HA antibodies prepared in vitro in the splenic fragment culture system. Three subgroups of antigenic variants were distinguished. The antigenic changes were primarily recognized by monoclonal antibodies to the strain- specific determinants of the parental hemagglutinin (HA) molecule. Monoclonal antibodies to HA determinants shared (in an identical or cross-reactive form) by parental virus and more than three heterologous viruses of the HON1 and H1N1 subtypes were unable to recognize the antigenic change on the variants. Similarly, heterogeneous antibody preparations could not differentiate between parental and variant viruses. The results are compatible with the idea that the HA of PR8 has available a large repertoire of antigenic modifications that may result from single amino acid substitutions, and that antigenic changes can occur in the strain- specific determinants on the HA molecule in the absence of concomitant changes in the cross-reactive HA determinants. The findings suggest that antigenic drift, in order to be epidemiologically significant, probably requires a series of amino acid substitutions in, or close to, the antigenic area on the HA molecule.
机译:在针对该病毒的单克隆抗体存在下,将亲代病毒单次传代到鸡胚中后,选择A / PR / 8/34 [HON1]流感病毒的抗原变体。单克隆抗体是由杂交瘤产生的,并且对亲本病毒的HA分子上的抗原决定簇具有特异性。用在脾脏片段培养系统中体外制备的95种单克隆抗HA抗体分析了七个抗原变体。区分了抗原变体的三个亚组。抗原变化主要由针对亲本血凝素(HA)分子的菌株特异性决定簇的单克隆抗体识别。亲本病毒和三种以上HON1和H1N1亚型异源病毒共享的HA决定簇单克隆抗体(以相同或交叉反应的形式)无法识别变体的抗原变化。同样,异种抗体制品无法区分亲本和变异病毒。结果与以下想法相符:PR8的HA具有可用的大量抗原修饰,这些抗原修饰可能是由单个氨基酸取代引起的,并且在不伴随HA分子的情况下,HA分子上的菌株特异性决定簇可能发生抗原变化交叉反应性HA决定因素的变化。这些发现表明,为了在流行病学上具有重要意义,抗原漂移可能需要在HA分子的抗原区域中或附近的一系列氨基酸取代。

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  • 作者

    Gerhard, W; Webster, RG;

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  • 年度 1978
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  • 原文格式 PDF
  • 正文语种 {"code":"en","name":"English","id":9}
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