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Cross-reactive variable-region associated epitopes of human IgG1 lambda paraprotein detected by a monoclonal antibody panel.

机译:通过单克隆抗体检测到的与人IgG1λ副蛋白交叉反应的可变区相关表位。

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摘要

This paper describes the production and characterization of a panel of 15 mouse monoclonal antibodies selected for putative activity against V-region related or allotypic determinants of a single IgG1 lambda paraprotein obtained from a patient with malignant lymphoplasmacytoid lymphoma. The specificity of each reagent for epitopes on the heavy (H) or light (L) chain or for conformational determinants (CD) of the immunogen was determined and the ability of one reagent to compete with another for these sites investigated. The fine specificity of the antibodies was assessed by screening on a large series of normal and paraprotein-containing sera. One monoclonal showed specificity for the Glm(f) allotype. The 14 other reagents identified a minimum of nine different epitopes in the V region of the immunogen, with four antibodies detecting private conformationally determined idiotypic specificities. Eight determinants were V-region markers also expressed on other paraproteins. A total of 30 out of 159 different paraproteins cross-reacted with one or more of the antibodies. Four of the shared epitopes were lambda-chain associated, three were H-chain associated and one was a conformational determinant. Homologies of lambda chain were identified more frequently among other paraproteins than those of H chain. The relationship between epitope expression and H-chain class of paraprotein was not random. The frequency of expression of cross-reactivities in association with IgG1 proteins was always exceeded by higher frequency of epitope expression in association with other classes of H-chain isotype. The potential therapeutic value of such panels of characterized monoclonal reagents is discussed.
机译:本文描述了一组15种小鼠单克隆抗体的生产和特性,这些单克隆抗体的选择是针对从患有恶性淋巴浆细胞样淋巴瘤的患者获得的单个IgG1λ副蛋白的V区相关或同种异型决定簇的推定活性。确定每种试剂对免疫原的重链(H)或轻链(L)上的表位或构象决定簇(CD)的特异性,并研究一种试剂与另一种试剂竞争这些位点的能力。通过在一系列正常和含副蛋白的血清中进行筛选,评估了抗体的精细特异性。一种单克隆抗体显示出对Glm(f)同种异型的特异性。其他14种试剂在免疫原的V区中至少鉴定了9种不同的表位,其中有4种抗体可检测私人构象确定的独特型特异性。八个决定簇是在其他副蛋白上也表达的V区标记。 159种不同的副蛋白中,共有30种与一种或多种抗体发生交叉反应。共有的表位中有四个是λ链相关的,三个是H链相关的,一个是构象决定簇。在其他副蛋白中,与H链相比,λ链的同源性更高。表位表达与副蛋白的H链类别之间的关系不是随机的。与IgG1蛋白相关的交叉反应性表达频率总是被与其他类别的H链同种型相关的更高的表位表达频率所超过。讨论了此类特征性单克隆试剂的潜在治疗价值。

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