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Immunoglobulin heavy chain constant regions regulate immunity and tolerance to idiotypes of antibody variable regions

机译:免疫球蛋白重链恒定区调节对抗体可变区独特型的免疫力和耐受性

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摘要

Particular syngeneic adjuvant-free monoclonal antibodies are immunogenic and elicit antibody responses against the variable region idiotypes (Ids). We here study how heavy-chain constant regions (CH) regulate immune responses to Ids of free, uncomplexed monoclonal antibodies. To this end, we selected two hybridomas, called Id3 and IdA.01, that produce immunogenic IgMλ2 directed toward 2,4,6-trinitrophenyl, and subcloned rare IgG1, IgG3, IgE, or IgA class switch variants. The purified switch variants, which possessed the Ids of their IgM progenitors, were injected repeatedly without added adjuvant into BALB/c mice, and anti-Id IgG responses were determined. These repeated injections revealed that the immunogenicity of Ids was lost by switching to IgG1 and IgG3, restored when the Fc piece of IgG1 was removed, maintained by switching to IgE and monomeric IgA, and lost in polymeric IgA. Loss of immunogenicity was associated with acquisition of Id-specific tolerogenicity, as determined by immunization challenge with Id borne by IgM. An Id borne by IgG induced tolerance when injected at least 90 days before or 3–21 days after immunization with IgM Id was begun. Ids of IgG were also tolerogenic in mice deficient in FcγRIIB or FcγRI + III. The results suggest that Ids that have switched to IgG and pIgA negatively control immune responses to shared Ids, including the Ids of their IgM progenitors.
机译:特定的无同源无佐剂的单克隆抗体具有免疫原性,并引发针对可变区独特型(Ids)的抗体反应。我们在这里研究重链恒定区(CH)如何调节对游离,未复合单克隆抗体Ids的免疫反应。为此,我们选择了两个杂交瘤,分别称为Id3和IdA.01,它们产生针对2,4,6-三硝基苯基的免疫原性IgMλ2,并亚克隆了罕见的IgG1,IgG3,IgE或IgA类开关变体。将具有其IgM祖细胞IDs的纯化的开关变体不加佐剂的情况下反复注射到BALB / c小鼠中,并测定抗Id IgG反应。这些重复的注射显示,通过转换为IgG1和IgG3,Ids的免疫原性丧失了;当IgG1的Fc片段被去除时,Ids的免疫原性得以恢复;通过转换为IgE和单体IgA得以维持,而在聚合IgA中则失去了Ids的免疫原性。免疫原性的丧失与获得Id特异的耐受性有关,这是由IgM携带的Id进行免疫攻击所确定的。当至少在免疫IgM Id之前90天或之后3-21天注射时,由IgG携带的Id会诱导耐受。在缺乏FcγRIIB或FcγRI+ III的小鼠中,IgG的Ids也具有耐受性。结果表明,已转换为IgG和pIgA的Id负控制了对共享Id(包括其IgM祖细胞的Ids)的免疫反应。

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