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用抗独特型抗体诱导对流感病毒的免疫应答。

Induction of immune response to influenza virus with anti-idiotypic antibodies.

作者信息

Anders E M, Kapaklis-Deliyannis G P, White D O

机构信息

Department of Microbiology, University of Melbourne, Parkville, Victoria, Australia.

出版信息

J Virol. 1989 Jun;63(6):2758-67. doi: 10.1128/JVI.63.6.2758-2767.1989.

Abstract

Anti-idiotypic (anti-Id) antibodies were raised in rabbits against five monoclonal antibodies (MAbs) specific for different antigenic sites on the hemagglutinin (HA) of influenza virus Mem71H-BelN (H3N1) [A/Memphis/1/71 (H3N2) x A/Bel/42 (H1N1)]. Each of the anti-Id sera was directed predominantly towards a unique (private) idiotype of the immunizing MAb, none of the five idiotypes being detectable in pooled BALB/c antisera against Mem71H-BelN virus or on most other anti-HA MAbs tested. Partial idiotypic sharing was observed, however, between certain MAbs, from different mice, having the same or similar epitope specificity for HA. When used as immunogens in BALB/c mice, two of the five anti-Id preparations induced antibodies that reacted with Mem71H-BelN virus and displayed neutralizing activity. Mice of other inbred strains responded similarly, indicating that the response was not genetically restricted by the Igh locus. From their pattern of reactivity with mutants of Mem71H-BelN virus with known single amino acid substitutions in the HA molecule, the antiviral antibodies elicited by anti-Id antibodies were shown to be directed to the same antigenic site on A/Memphis/1/71 HA as the original immunizing MAb (site A or site E, respectively). However, several of these antisera were shown to contain additional distinct subpopulations of antibodies specific for heterologous influenza A virus strains, either of the H3 subtype or of a different HA subtype (H1 or H2). Since the induction of antibodies to HA of different subtypes is not a feature of the antibody response to influenza virus itself, their induction by anti-Id antibodies merits further investigation.

摘要

用针对流感病毒Mem71H - BelN(H3N1)[A/孟菲斯/1/71(H3N2)×A/比利时/42(H1N1)]血凝素(HA)上不同抗原位点的五种单克隆抗体(MAb)在兔体内制备抗独特型(抗Id)抗体。每种抗Id血清主要针对免疫用MAb的一种独特(私有)独特型,在针对Mem71H - BelN病毒的BALB/c混合抗血清或大多数其他测试的抗HA MAb中均未检测到这五种独特型中的任何一种。然而,在某些对HA具有相同或相似表位特异性的不同小鼠来源的MAb之间观察到了部分独特型共享。当作为免疫原用于BALB/c小鼠时,五种抗Id制剂中的两种诱导出了与Mem71H - BelN病毒反应并具有中和活性的抗体。其他近交系小鼠也有类似反应,表明该反应不受Igh基因座的遗传限制。根据它们与HA分子中已知单氨基酸取代的Mem71H - BelN病毒突变体的反应模式,抗Id抗体引发的抗病毒抗体被证明与原始免疫用MAb针对A/孟菲斯/1/71 HA上的相同抗原位点(分别为位点A或位点E)。然而,这些抗血清中有几种被证明含有针对异源甲型流感病毒株的其他不同抗体亚群,这些病毒株要么是H3亚型,要么是不同的HA亚型(H1或H2)。由于诱导针对不同亚型HA的抗体不是对流感病毒本身抗体反应的特征,抗Id抗体对其的诱导值得进一步研究。

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