Yamamoto H, Nonaka M, Katz D H
J Exp Med. 1979 Oct 1;150(4):818-29. doi: 10.1084/jem.150.4.818.
Delayed-type hypersensitivity (DTH) responses specific for the phosphorylcholine (PC) hapten were induced in BALB/c mice by immunization with syngeneic peritoneal exudate cells (PEC) coupled with diazotized phenyl-phosphoryl-choline. PC-specific DTH responses were elicited in such immunized mice after footpad challenge with PC-derivatized syngeneic spleen cells. Moreover, PC-immune lymph node cells could passively transfer PC-specific DTH responses to naive BALB/c mice and it was possible to demonstrate that the cells responsible for such passively transferred responses were T lymphocytes. Because the T-15 idiotypic determinant displayed on the TEPC-15 PC-binding myeloma protein is known to be a dominant idiotype associated with anti-PC antibody responses in BALB/c mice, an analysis was made of the effects of anti-T-15 idiotypic antibodies on the induction and expression of murine PC-specific DTH responses. Repeated injections of anti-T-15 idiotypic antiserum, raised in A/J mice by immunization with TEPC-15 myeloma protein, into recipient BALB/c mice both immediately before and after sensitization with PC-PEC virtually abolished the development of PC-specific DTH responses. Although administration of anti-T-15 antiserum effectively inhibited the induction phase of PC-specific DTH responses, these anti-idiotypic antibodies had no suppressive activity at the effector phase of these responses. The inhibition observed with anti-T-15 antibodies was highly specific for the PC hapten, and for PC-specific DTH responses of BALB/c but not A/J mice. Studies were conducted to address the possibility that anti-Id treatment induced suppressor T lymphocytes capable of specifically inhibiting the activity of PC-specific T cells participating in DTH responses. The results demonstrate that idiotype-specific suppressor T cells are, indeed, induced by treatment with anti-Id; moreover, such suppressor T cells, once induced, are highly effective in abrogating both the induction and the effector phases of PC-specific T cell-mediated DTH responses in BALB/c mice.
通过用重氮化苯基 - 磷酰胆碱偶联的同基因腹膜渗出细胞(PEC)免疫BALB/c小鼠,诱导了对磷酰胆碱(PC)半抗原的迟发型超敏反应(DTH)。在用PC衍生的同基因脾细胞进行足垫攻击后,在这种免疫小鼠中引发了PC特异性DTH反应。此外,PC免疫淋巴结细胞可以将PC特异性DTH反应被动转移到未免疫的BALB/c小鼠中,并且有可能证明负责这种被动转移反应的细胞是T淋巴细胞。因为已知在TEPC - 15 PC结合骨髓瘤蛋白上显示的T - 15独特型决定簇是与BALB/c小鼠中抗PC抗体反应相关的主要独特型,所以分析了抗T - 15独特型抗体对小鼠PC特异性DTH反应的诱导和表达的影响。在用PC - PEC致敏之前和之后,立即将通过用TEPC - 15骨髓瘤蛋白免疫A/J小鼠产生的抗T - 15独特型抗血清重复注射到受体BALB/c小鼠中,几乎消除了PC特异性DTH反应的发展。虽然抗T - 15抗血清的给药有效地抑制了PC特异性DTH反应的诱导阶段,但这些抗独特型抗体在这些反应的效应阶段没有抑制活性。用抗T - 15抗体观察到的抑制对PC半抗原以及对BALB/c小鼠而非A/J小鼠的PC特异性DTH反应具有高度特异性。进行了研究以探讨抗独特型治疗是否诱导了能够特异性抑制参与DTH反应的PC特异性T细胞活性的抑制性T淋巴细胞的可能性。结果表明,抗独特型治疗确实诱导了独特型特异性抑制性T细胞;此外,这种抑制性T细胞一旦被诱导,在消除BALB/c小鼠中PC特异性T细胞介导的DTH反应的诱导和效应阶段方面非常有效。