Lonai P, Ben-Neriah Y, Steinman L, Givol D
Eur J Immunol. 1978 Dec;8(12):827-32. doi: 10.1002/eji.1830081202.
Antigen-binding inhibition studies using microscopic autoradiography were performed on T or B cell-enriched lymphocyte populations. Antibodies specific for the "framework" of immunoglobulin heavy or light chain variable domains (VH or VL), or anti-H-2 and anti-Ia antisera were used. T cell subclasses were separated with anti-Lyt antisera and complement. It was found that antigen-binding T cells of different subclasses can be inhibited selectively with only one of the two anti-V region antibodies. Antigen binding to Lyt-1+ cells was inhibited by anti-VH, while Lyt-2+,3+ cells were inhibited by anti-VL specifically. Anti-Ia antisera inhibited unprimed Lyt-1+ antigen-binding cells, whereas anti-H-2K or anti-H-2D anti-sera inhibited unprimed Lyt-2+,3+ antigen-binding cells, and both classes of immune T antigen-binding cells.
利用显微放射自显影术对富含T细胞或B细胞的淋巴细胞群体进行了抗原结合抑制研究。使用了针对免疫球蛋白重链或轻链可变区(VH或VL)“构架”的特异性抗体,以及抗H-2和抗Ia抗血清。用抗Lyt抗血清和补体分离T细胞亚类。结果发现,仅用两种抗V区抗体中的一种就能选择性地抑制不同亚类的抗原结合T细胞。抗VH抑制与Lyt-1+细胞的抗原结合,而抗VL则特异性抑制Lyt-2+、3+细胞。抗Ia抗血清抑制未致敏的Lyt-1+抗原结合细胞,而抗H-2K或抗H-2D抗血清抑制未致敏的Lyt-2+、3+抗原结合细胞以及两类免疫T抗原结合细胞。