首页> 美国卫生研究院文献>The Journal of Experimental Medicine >Generation and decay of the immune response to a progressive fibrosarcoma. I. Ly-1+2- suppressor T cells down-regulate the generation of Ly-1-2+ effector T cells
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Generation and decay of the immune response to a progressive fibrosarcoma. I. Ly-1+2- suppressor T cells down-regulate the generation of Ly-1-2+ effector T cells

机译:对进行性纤维肉瘤的免疫反应的产生和衰减。 I. Ly-1 + 2-抑制性T细胞下调Ly-1-2 +抑制性T细胞的生成

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摘要

It was shown that the progressive growth of the immunogenic meth A fibrosarcoma in its semisyngeneic host results in the generation of concomitant immunity to the growth of a tumor implant. The generation of immunity occurred between days 6 and 9 of tumor growth and was associated with the generation of sensitized T cells that were capable, on passive transfer, of causing regression of a 3-d tumor in gamma- irradiated recipients. After day 9 of tumor growth, concomitant immunity and the T cells able to passively transfer it were progressively lost, and this was associated with the generation of splenic suppressor T cells able to suppress the expression of adoptive immunity against an established tumor in T cell-deficient ( TXB ) recipients. The T cells that passively transferred concomitant immunity were shown to be of the Ly-1-2+ phenotype, in contrast to the T cells that transferred suppression, which were shown with the same reagents to be Ly-1+2-. The results are consistent with the hypothesis that the progressive growth of an immunogenic tumor results in the generation of Ly-1-2+-sensitized effector T cells that fail to reach a number sufficient to destroy the tumor because their generation is down- regulated by tumor-induced Ly-1+2- suppressor T cells.
机译:已经表明,免疫原性甲基A纤维肉瘤在其半同基因宿主中的逐渐生长导致伴随着对肿瘤植入物生长的免疫的产生。免疫力的产生发生在肿瘤生长的第6天至第9天之间,并与致敏的T细胞产生有关,这些T细胞能够在被动转移时引起受伽马射线照射的受体消退3-d肿瘤。肿瘤生长的第9天后,伴随的免疫力和能够被动转移的T细胞逐渐丧失,这与脾抑制性T细胞的产生有关,脾脏抑制性T细胞能够抑制针对已建立的肿瘤的T细胞中过表达的免疫表达。缺陷(TXB)收件人。被动转移伴随免疫的T细胞显示为Ly-1-2 +表型,而转移抑制表达的T细胞则与相同的试剂显示为Ly-1 + 2-。该结果与以下假设相符:免疫原性肿瘤的进行性生长导致产生Ly-1-2 +敏感的效应T细胞,该细胞未能达到足以破坏肿瘤的数量,因为它们的生成受下调。肿瘤诱导的Ly-1 + 2-抑制性T细胞。

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