Cammisuli S, Cosenza H
Eur J Immunol. 1980 Apr;10(4):299-304. doi: 10.1002/eji.1830100414.
In the absence of the homologous antigen, an anti-phosphorylcholine (PC) plaque-forming cell (PFC) response has been induced in vitro which is restricted to the TEPC 15 idiotype (T15). Anti-T15 antibodies were used to focus either the keyhole limpet hemocyanin (KLH) or the fowl gamma-globulin (FGG) carrier molecules on the membrane of B cells carrying the T15 idiotype on their immunoglobulin receptors; thereafter, these cells were allowed to cooperate in vitro for 5 days with T cells primed to the appropriate carrier molecule. A response, virtually 100% T15+, could be induced both in normal BALB/c and in T15 neonatally suppressed mice which had lost the T15+ clonal dominance. The magnitude of this response is comparable to that obtained in the presence of the PC antigen. The role of the membrane-bound immunoglobulin receptor (sIg) in the expression of different anti-PC clones was also investigated. We have focused either the KLH or the FGG carrier molecules on the membrane of B cells via anti-H-2 antibodies and then cultured these cells for 5 days with the appropriate carrier-specific T cells. Under these conditions, B cells are activated in the absence of interaction at the sIg. The idiotypic profile of the anti-PC PFC obtained with the anti-H-2-mediated activation was then compared with the profile of the anti-PC response obtained in the presence of PC antigen. Since similar idiotypic profiles were obtained in both cases, it can be excluded that sIg plays a direct role in favoring the expression of T15+ over T15- anti-PC clones.
在缺乏同源抗原的情况下,已在体外诱导出抗磷酸胆碱(PC)的空斑形成细胞(PFC)反应,该反应限于TEPC 15独特型(T15)。抗T15抗体用于将钥孔戚血蓝蛋白(KLH)或鸡γ球蛋白(FGG)载体分子聚焦于免疫球蛋白受体上携带T15独特型的B细胞膜上;此后,让这些细胞在体外与用适当载体分子致敏的T细胞协同作用5天。在正常BALB/c小鼠和已丧失T15+克隆优势的新生期受T15抑制的小鼠中均可诱导出几乎100%为T15+的反应。该反应的强度与在有PC抗原存在时所获得的强度相当。还研究了膜结合免疫球蛋白受体(sIg)在不同抗PC克隆表达中的作用。我们已通过抗H-2抗体将KLH或FGG载体分子聚焦于B细胞膜上,然后将这些细胞与适当的载体特异性T细胞一起培养5天。在这些条件下,B细胞在没有sIg相互作用的情况下被激活。然后将通过抗H-2介导的激活所获得的抗PC PFC的独特型谱与在有PC抗原存在时所获得的抗PC反应的谱进行比较。由于在两种情况下均获得了相似的独特型谱,因此可以排除sIg在促进T15+抗PC克隆而非T15-抗PC克隆表达方面起直接作用。