Lerner E A, Matis L A, Janeway C A, Jones P P, Schwartz R H, Murphy D B
J Exp Med. 1980 Oct 1;152(4):1085-101. doi: 10.1084/jem.152.4.1085.
Genetic, biochemical, and functional studies have been performed using a monoclonal antibody, Y-17, directed at a conformational or combinatorial determinant formed by certain Ae:E alpha complexes. This determinant appears to be a marker present on a subset of B cells as well as on non-T and non-B spleen cells. Besides Ae and E alpha chains, Y-17 precipitates a third chain that is indistinguishable from the A alpha chain in two-dimensional gels. This results suggests additional combinatorial complexity in the generation of I-region encoded antigens. Y-17 can inhibit the response of T cells to Ae:E alpha determinants in mixed lymphocyte cultures. Furthermore, Y-17 blocks antigen-specific T cell proliferative responses to GLPhe and pigeon cytochrome c which have been shown to require the Ae:E alpha complex as a restriction element for antigen presentation. These results provide strong evidence for the molecular identity of Ia antigens, Ir-gene products and Lad antigens.
利用一种单克隆抗体Y - 17开展了遗传学、生物化学和功能研究,该抗体针对由某些Ae:Eα复合物形成的构象或组合决定簇。这个决定簇似乎是存在于一部分B细胞以及非T和非B脾细胞上的一种标志物。除了Ae和Eα链外,Y - 17沉淀出第三条链,在二维凝胶中它与Aα链无法区分。这一结果表明在I区编码抗原的产生过程中存在额外的组合复杂性。Y - 17能够在混合淋巴细胞培养物中抑制T细胞对Ae:Eα决定簇的反应。此外,Y - 17阻断了T细胞对GLPhe和鸽细胞色素c的抗原特异性增殖反应,已表明这需要Ae:Eα复合物作为抗原呈递的限制元件。这些结果为Ia抗原、Ir基因产物和Lad抗原的分子同一性提供了有力证据。