首页> 外文OA文献 >Regulatory functions of hapten-reactive helper and suppressor T lymphocytes. III. Amplification of a generation of tumor-specific killer T-lymphocyte activities by suppressor T-cell-depleted hapten- reactive T lymphocytes
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Regulatory functions of hapten-reactive helper and suppressor T lymphocytes. III. Amplification of a generation of tumor-specific killer T-lymphocyte activities by suppressor T-cell-depleted hapten- reactive T lymphocytes

机译:半抗原反应性辅助和抑制性T淋巴细胞的调节功能。三,通过抑制性T细胞缺失的半抗原反应性T淋巴细胞扩增肿瘤特异性杀伤性T淋巴细胞活性的产生

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摘要

2,4.6-trinitrophenyl (TNP)-reactive T-cell activities were raised in mice by immunization with TNP-isologous mouse gamma globulin. After establishing that TNP-reactive T lymphocytes can serve as amplifier cells for induction of killer T lymphocytes in allogeneic system, we explored the possibility of this hapten-reactive T-cell system to amplify tumor-specific killer T-lymphocyte activity in the syngeneic system. We utlized relatively weak immunogenic syngeneic plasmacytoma X5563 in C3H/He mice. Analysis of the TNP-reactive T-cell activities revealed that such T lymphocytes express the biological functions of both major subtypes of regulatory T cells, namely suppressors and helpers, and that TNP-reactive suppressor and helper T lymphocytes, respectively, differ in their relative susceptibility to specific inactivation by TNP conjugates of the nonimmunogenic D-amino acid copolymer, D-glutamic acid, and D-lysine (D-GL). By taking advantage of the relative susceptibility-difference to TNP-D-GL, selective inactivation of TNP-reactive suppressor T cells was induced by appropriate treatment with TNP-D-GL, and the generation of TNP-reactive helper T-cell activity was amplified. The supplement of augmented TNP- reactive helper T-cell activity to the system at the immunization with syngeneic X5563 with TNP-haptenation, resulted in a striking augmentation of induction of tumor-specific killer T-lymphocyte activity, and a considerable number of hosts survived after the challenge with lethal dose of viable tumor cells. Thus, appropriate manipulations designed to induce potent hapten-reactive helper T- lymphocytes provided the potential for a very effective mode of immunoprophylaxis against tumor.
机译:通过用TNP同源的小鼠丙种球蛋白免疫,可提高小鼠的2,4.6-三硝基苯基(TNP)反应性T细胞活性。在确定TNP反应性T淋巴细胞可以用作同种异体系统中诱导杀伤性T淋巴细胞的扩增细胞后,我们探索了这种半抗原反应性T细胞系统在同系系统中扩增肿瘤特异性杀伤性T淋巴细胞活性的可能性。 。我们在C3H / He小鼠中使用了相对较弱的免疫原性同质浆细胞瘤X5563。对TNP反应性T细胞活性的分析表明,此类T淋巴细胞表达调节性T细胞的两种主要亚型的生物学功能,即抑制子和辅助T细胞,而TNP反应性抑制子和辅助T淋巴细胞的相对功能分别不同。非免疫原性D-氨基酸共聚物,D-谷氨酸和D-赖氨酸(D-GL)的TNP偶联物对特定灭活的敏感性。利用相对于TNP-D-GL的相对敏感性差异,通过适当处理TNP-D-GL诱导TNP反应性抑制性T细胞选择性失活,从而产生TNP反应性辅助性T细胞活性。放大。用同基因X5563进行TNP半抗原免疫后向系统补充增强的TNP反应性辅助性T细胞活性,导致对肿瘤特异性杀伤性T淋巴细胞活性的诱导显着增加,并且大量宿主得以幸存用致死剂量的活肿瘤细胞攻击后。因此,设计用于诱导强力半抗原反应性辅助T淋巴细胞的适当操作为针对肿瘤的免疫预防非常有效的模式提供了潜力。

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