首页> 美国卫生研究院文献>Immunology >Regulation of immune responses against the syngeneic ADJ-PC-5 plasmacytoma in BALB/c mice. II. Suppression of T-cell cytotoxicity by pretreatment of mice with subimmunogenic doses of tumour cells.
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Regulation of immune responses against the syngeneic ADJ-PC-5 plasmacytoma in BALB/c mice. II. Suppression of T-cell cytotoxicity by pretreatment of mice with subimmunogenic doses of tumour cells.

机译:调节BALB / c小鼠针对同基因ADJ-PC-5浆细胞瘤的免疫应答。二。通过用亚免疫原剂量的肿瘤细胞预处理小鼠来抑制T细胞的细胞毒性。

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摘要

Protective immunity towards a lethal dose of 10(4) living ADJ-PC-5 cells can be induced in 56% of BALB/c mice by treating them with 10(7) irradiated cells. This protection can be modulated by pretreatment of animals with lower numbers of irradiated tumour cells. Repeated injections of 10(1) cells before immunization and challenge with tumour cells lead to tumours in only 16% of the animals, whereas repeated injections of 10(5) cells shift the tumour incidence to 78%. The enhanced tumour incidence is paralleled by suppression of T-cell cytotoxicity which can be transferred by spleen cells into 100 r-irradiated BALB/c mice. The possible significance of induction of specific immunosuppression during the initial stages of tumour growth is discussed. It is stressed that this suppression becomes effective at a dose 10(3) times lower than that which could induce protective immunity.
机译:通过用10(7)照射的细胞处理,可以在56%的BALB / c小鼠中诱导对致死剂量的10(4)个活ADJ-PC-5细胞的保护性免疫。可以通过用较少数量的辐射肿瘤细胞预处理动物来调节这种保护作用。免疫前反复注射10(1)细胞并用肿瘤细胞攻击仅在16%的动物中导致肿瘤,而反复注射10(5)细胞则将肿瘤发生率转移到78%。增加的肿瘤发生率与抑制T细胞的细胞毒性同时发生,脾细胞可以将T细胞的细胞毒性转移到100只r射线照射的BALB / c小鼠体内。讨论了在肿瘤生长的初始阶段诱导特异性免疫抑制的可能意义。要强调的是,这种抑制作用的剂量比可能诱导保护性免疫的剂量低10(3)倍。

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