Parhami-Seren B, Strassmann G, Mozes E, Sela M
Proc Natl Acad Sci U S A. 1982 Sep;79(18):5636-40. doi: 10.1073/pnas.79.18.5636.
The crossreactivity between the random synthetic polypeptide antigen poly(Tyr,Glu)-poly(DLAla)--poly(Lys) [(T,G)-A--L] and its ordered-sequence analogs (Tyr-Tyr-Glu-Glu)-poly(DLAla)--poly(Lys) [(T-T-G-G)-A--L] and (Tyr-Glu-Tyr-Glu)-poly(DLAla)--poly(Lys) [(T-G-T-G)-A--L] at the level of humoral and cellular responses was studied. For delayed type hypersensitivity responses, (T,G)-A--L-activated T cells could be challenged with the homologous antigen as well as with the ordered analogs. T cells activated by (T-T-G-G)-A--L could be challenged with either the homologous antigen or with (T,G)-A--L but not with (T-G-T-G)-A--L. Similarly, no cross stimulation was observed between (T-G-T-G)-A--L-activated cells and (T-T-G-G)-A--L, whereas (T,G)-A--L could challenge the latter cells to mediate significant responses. Similar but not identical cross reactions were observed when primed spleen cells or lymph nodes were transferred to irradiated recipients that were boosted for the production of antibodies. In contrast to observations at the level of cellular responses, (T-G-T-G)-A--L-primed spleen or lymph node cells could not be boosted with (T,G)-A--L for the production of detectable amounts of antibodies, although boosting with the homologous antigen resulted in significant levels of (T-G-T-G)-A--L-specific antibodies. Transfer experiments in which mixtures of T and B cells, each primed to a different ordered polypeptide antigen, were injected into irradiated recipients showed that successful cooperation occurs provided that the boost is given with the T-cell-specific antigen. The antibodies produced were specific to the antigen used for B-cell priming. The T-cell-B-cell collaboration probably occurs through specific determinants that are shared between the two antigens in which the ordered peptides are attached to the same multichain polymer and that are recognized by both the T and the B cells.
研究了随机合成多肽抗原聚(酪氨酸,谷氨酸)-聚(D-丙氨酸)-聚(赖氨酸)[(T,G)-A-L]与其有序序列类似物(酪氨酸-酪氨酸-谷氨酸-谷氨酸)-聚(D-丙氨酸)-聚(赖氨酸)[(T-T-G-G)-A-L]和(酪氨酸-谷氨酸-酪氨酸-谷氨酸)-聚(D-丙氨酸)-聚(赖氨酸)[(T-G-T-G)-A-L]在体液和细胞反应水平上的交叉反应性。对于迟发型超敏反应,(T,G)-A-L激活的T细胞可以用同源抗原以及有序类似物进行攻击。由(T-T-G-G)-A-L激活的T细胞可以用同源抗原或(T,G)-A-L进行攻击,但不能用(T-G-T-G)-A-L进行攻击。同样,在(T-G-T-G)-A-L激活的细胞和(T-T-G-G)-A-L之间未观察到交叉刺激,而(T,G)-A-L可以刺激后者细胞介导显著反应。当将致敏的脾细胞或淋巴结转移到经辐射的受体中以促进抗体产生时,观察到了相似但不完全相同的交叉反应。与细胞反应水平的观察结果相反,(T-G-T-G)-A-L致敏的脾或淋巴结细胞不能用(T,G)-A-L进行刺激以产生可检测量的抗体,尽管用同源抗原进行刺激会导致产生显著水平的(T-G-T-G)-A-L特异性抗体。将分别致敏于不同有序多肽抗原的T细胞和B细胞混合物注射到经辐射的受体中的转移实验表明,只要用T细胞特异性抗原进行加强免疫,就会发生成功的合作。产生的抗体对用于B细胞致敏的抗原具有特异性。T细胞与B细胞的协作可能是通过两种抗原之间共享得特异性决定簇发生的,其中有序肽连接到同一多链聚合物上,并且T细胞和B细胞均可识别。