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具有不同抗原特异性的MRL单克隆自身抗体之间的独特型交叉反应。

Idiotypic cross-reaction between MRL monoclonal autoantibodies with different antigen specificity.

作者信息

Pisetsky D S, Caster S A

出版信息

Clin Immunol Immunopathol. 1984 Mar;30(3):461-8. doi: 10.1016/0090-1229(84)90031-x.

Abstract

The idiotypic determinants borne by Y2, a monoclonal anti-SM antibody of MRL mouse strain origin, were investigated to elucidate mechanisms for the generation of autoantibodies. Using an ELISA assay, a rabbit anti-Y2 anti-idiotypic antiserum was tested for binding to other MRL autoantibodies to identify cross-reactive determinants. In this way, a shared idiotype was demonstrated for Y2 and 4K1, 4k1 is an IgG2bK monoclonal antibody derived from a fusion with spleen cells of an MRL-lpr/lpr mouse expressing anti-Sm. 4K1 displayed an antigenic specificity distinct from anti-Sm, however, with reactivity by fluorescent antinuclear antibody analysis to a subcellular component localized to the perinuclear region. The expression of the Y2-4K1 idiotype was assessed using a sensitive inhibition ELISA. The Y2-4K1 determinant was present in sera of MRL-lpr/lpr mice irrespective of the presence of anti-Sm. Sera of some but not all normal mouse strains also demonstrated this determinant. These results indicate that while some idiotypes may be associated with autoantibodies, they are not restricted to the autoimmune setting. This pattern of expression suggests that autoantibodies are part of larger idiotype-bearing antibody families with structural similarity to antibodies produced by normal mice. The autoimmune setting may promote the emergence of idiotype-bearing molecules with autoantibody activity and aberrant regulation.

摘要

为了阐明自身抗体产生的机制,对源自MRL小鼠品系的单克隆抗Sm抗体Y2所携带的独特型决定簇进行了研究。使用酶联免疫吸附测定(ELISA),检测兔抗Y2抗独特型抗血清与其他MRL自身抗体的结合情况,以鉴定交叉反应性决定簇。通过这种方式,证明了Y2和4K1具有共同的独特型,4K1是一种IgG2bK单克隆抗体,源自与表达抗Sm的MRL-lpr/lpr小鼠的脾细胞融合。然而,4K1显示出与抗Sm不同的抗原特异性,通过荧光抗核抗体分析,它与定位于核周区域的亚细胞成分发生反应。使用灵敏的抑制ELISA评估Y2-4K1独特型的表达。无论抗Sm是否存在,Y2-4K1决定簇都存在于MRL-lpr/lpr小鼠的血清中。一些但并非所有正常小鼠品系的血清也显示出这种决定簇。这些结果表明,虽然一些独特型可能与自身抗体相关,但它们并不局限于自身免疫环境。这种表达模式表明,自身抗体是更大的携带独特型抗体家族的一部分,与正常小鼠产生的抗体具有结构相似性。自身免疫环境可能促进具有自身抗体活性和异常调节的携带独特型分子的出现。

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