Gleason K, Pierce S, Köhler H
J Exp Med. 1981 Apr 1;153(4):924-35. doi: 10.1084/jem.153.4.924.
Different manipulations of BALB/c mice were used to generate idiotype-specific help: neonatally induced suppression of the T 15 idiotype and low-dose priming with anti-T15 antibody. The splenic foci culture system was used to study T15-idiotype-recognizing helper T cells under limiting-cell-dose conditions. These treatments induced T15 idiotype-specific help for B cells responding to TNP-T15. Normal or hemocyanin-primed BALB/c mice did not supply T15 idiotype-specific help. The helper cells were sensitive to anti-Thy-1.2 and complement treatment and can distinguish T15 from an idiotype-different, PC-binding myeloma protein, M167, and the TNP binding myeloma protein, M460. These data show that idiotype-specific T helper cells can be induced by at least two different manipulations of the idiotype network. These manipulations presumably do not act directly on the T15-recognizing T cells, but must involve complementary idiotypic circuits that stimulate anti-T15 specific T cells. Furthermore, this study demonstrates that the splenic-fragment culture technique provides a general method to investigate, at the single cell level, idiotypic T-B cell interactions induced by perturbations of the immune network.
采用不同的方法处理BALB/c小鼠以产生独特型特异性辅助:新生期诱导T15独特型抑制和用抗T15抗体进行低剂量启动。利用脾灶培养系统在有限细胞剂量条件下研究识别T15独特型的辅助性T细胞。这些处理诱导了针对对TNP-T15作出反应的B细胞的T15独特型特异性辅助。正常或经血蓝蛋白启动的BALB/c小鼠不提供T15独特型特异性辅助。这些辅助性细胞对抗Thy-1.2和补体处理敏感,并且能够区分T15与独特型不同的、结合PC的骨髓瘤蛋白M167以及结合TNP的骨髓瘤蛋白M460。这些数据表明,独特型特异性T辅助细胞可通过独特型网络的至少两种不同处理诱导产生。这些处理大概不是直接作用于识别T15的T细胞,而是必定涉及刺激抗T15特异性T细胞的互补独特型回路。此外,本研究证明,脾片段培养技术提供了一种在单细胞水平研究免疫网络扰动诱导的独特型T-B细胞相互作用的通用方法。