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一系列小鼠B细胞淋巴瘤所表达的交叉反应性独特型和共同抗原结合特异性:病因学意义

Cross-reactive idiotypes and common antigen binding specificities expressed by a series of murine B-cell lymphomas: etiological implications.

作者信息

Pennell C A, Arnold L W, Lutz P M, LoCascio N J, Willoughby P B, Haughton G

出版信息

Proc Natl Acad Sci U S A. 1985 Jun;82(11):3799-803. doi: 10.1073/pnas.82.11.3799.

Abstract

A series of 27 B-cell lymphomas (designated the CH series), induced in B10.H-2aH-4b p/Wts mice by intense adoptive immunization with sheep erythrocytes, was found to represent a subset of the total B-cell repertoire. This subset was characterized by expression of a limited number of Ig heavy chain variable regions, as evidenced by the presence of cross-reactive idiotypes and common antigen binding specificities. Twenty-one of the 27 CH lymphomas studied were classified into five groups, defined by a particular cross-reactive idiotype; four of these groups were linked in a single network. Seven of 16 idiotypes defined by absorption analysis were present on lymphomas bearing either kappa or lambda light chains and so were localized to the heavy chain variable region. The surface Ig on 14 CH lymphomas was found to be specific for epitopes on certain erythrocytes (bromelain-treated autologous erythrocytes, sheep, and chicken erythrocytes) or E. coli. We propose that the CH lymphomas represent the malignant counterparts of a subset of idiotypically related, normal B cells in B10.H-2aH-4b p/Wts mice. Perturbation of this idiotype network, by hyperimmunization with an antigen for which some of the members are specific (sheep erythrocytes), increases the risk for neoplasia. Possible mechanisms for this are discussed.

摘要

通过用绵羊红细胞进行强烈的过继免疫在B10.H-2aH-4b p/Wts小鼠中诱导产生了一系列27种B细胞淋巴瘤(命名为CH系列),发现它们代表了整个B细胞库的一个子集。该子集的特征是表达有限数量的Ig重链可变区,交叉反应性独特型和共同抗原结合特异性的存在证明了这一点。所研究的27种CH淋巴瘤中有21种被分为五组,由特定的交叉反应性独特型定义;其中四组连接在一个单一网络中。通过吸收分析确定的16种独特型中有7种存在于携带κ或λ轻链的淋巴瘤上,因此定位于重链可变区。发现14种CH淋巴瘤上的表面Ig对某些红细胞(菠萝蛋白酶处理的自体红细胞、绵羊和鸡红细胞)或大肠杆菌上的表位具有特异性。我们提出,CH淋巴瘤代表了B10.H-2aH-4b p/Wts小鼠中一组独特型相关的正常B细胞的恶性对应物。用一些成员具有特异性的抗原(绵羊红细胞)进行超免疫会扰乱这个独特型网络,增加肿瘤形成的风险。本文讨论了可能的机制。

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