Mariani S M, Armandola E A, Ferrone S
Department of Microbiology and Immunology, New York Medical College, Valhalla 10595.
Transplantation. 1993 May;55(5):1176-81. doi: 10.1097/00007890-199305000-00044.
In spite of the potential role of antiidiotypic (anti-id) antibodies in the immune response to mismatched HLA antigens and in the outcome of renal allografts, the idiotypic cascade in the HLA system has been characterized to a limited extent. For instance, it is not known whether anti-id antibodies defining idiotopes coexpressed in the combining site of the original anti-HLA antibody selectively stimulate distinct subsets of B cell clones. Since this information contributes to our understanding of the role of anti-id antibodies in the generation of diversity in anti-HLA immune response, we have determined whether a preferential recognition of the immunizing anti-id mAb is displayed by the two subsets of anti-HLA-DR mAb elicited with anti-id mAb F5-444 and F5-830. The latter two mAb recognize idiotopes coexpressed in the antigen-combining site of the immunizing anti-HLA-DR1,4,w14,w8,9 mAb AC1.59. All the anti-HLA-DR mAb elicited with mAb F5-830 displayed a higher functional affinity for the immunizing anti-id mAb than the anti-HLA-DR mAb elicited with mAb F5-444. This finding reflects the higher reactivity of the subset of anti-HLA-DR mAb elicited with mAb F5-830 with the light chain of the immunizing mAb. The present study, therefore, shows for the first time that distinct anti-id mAb recognizing idiotopes coexpressed in the combining site of anti-HLA-DR mAb stimulate different subsets of idiotope positive B cell clones in a nonrandom fashion. This preferential selection by anti-id mAb affects the characteristics of the immune response, as the two subsets of anti-HLA-DR mAb display differences in their fine specificity. These results are consistent with the possibility that anti-id antibodies may play a role in the changes in the specificity of anti-HLA antibodies that may occur in the course of an immune response to mismatched HLA alloantigens.
尽管抗独特型(抗Id)抗体在针对不匹配的HLA抗原的免疫反应以及肾移植结果中具有潜在作用,但HLA系统中的独特型级联反应在很大程度上尚未得到充分表征。例如,尚不清楚定义在原始抗HLA抗体结合位点中共表达的独特型的抗Id抗体是否选择性地刺激B细胞克隆的不同亚群。由于这些信息有助于我们理解抗Id抗体在抗HLA免疫反应多样性产生中的作用,我们已经确定了用抗Id单克隆抗体F5-444和F5-830诱导产生的抗HLA-DR单克隆抗体的两个亚群是否对免疫抗Id单克隆抗体表现出优先识别。后两种单克隆抗体识别在免疫抗HLA-DR1,4,w14,w8,9单克隆抗体AC1.59的抗原结合位点中共表达的独特型。与用单克隆抗体F5-444诱导产生的抗HLA-DR单克隆抗体相比,用单克隆抗体F5-830诱导产生的所有抗HLA-DR单克隆抗体对免疫抗Id单克隆抗体表现出更高的功能亲和力。这一发现反映了用单克隆抗体F5-830诱导产生的抗HLA-DR单克隆抗体亚群与免疫单克隆抗体轻链的更高反应性。因此,本研究首次表明,识别在抗HLA-DR单克隆抗体结合位点中共表达的独特型的不同抗Id单克隆抗体以非随机方式刺激独特型阳性B细胞克隆的不同亚群。抗Id单克隆抗体的这种优先选择影响免疫反应的特征,因为抗HLA-DR单克隆抗体的两个亚群在其精细特异性上存在差异。这些结果与抗Id抗体可能在针对不匹配的HLA同种异体抗原的免疫反应过程中抗HLA抗体特异性变化中发挥作用的可能性一致。