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对与鼠肉瘤病毒诱导肿瘤相关抗原的细胞介导免疫:通过体外连续特异性和非特异性刺激增强细胞毒性T淋巴细胞活性

Cell-mediated immunity to antigens associated with murine sarcoma virus-induced tumors: augmentation of cytolytic T lymphocyte activity by successive specific and nonspecific stimulation in vitro.

作者信息

Ryser J E, Cerottini J C, Brunner K T

出版信息

Eur J Immunol. 1979 Mar;9(3):179-84. doi: 10.1002/eji.1830090302.

Abstract

It has been shown previously that lymphoid cells from mice which have rejected a tumor induced by the Moloney sarcoma virus-leukemia virus (MSV-MLV) complex develop high levels of specific H-2-restricted cytolytic T lymphocyte (CTL) activity after in vitro stimulation with syngeneic, irradiated MLV-induced lymphoma cells in mixed leukocyte-tumor cell cultures (MLTC). Attempts to further increase lytic activity by restimulating long-term MLTC cells with syngeneic, irradiated lymphoma cells have met but with limited success. This report shows that, in contrast to the lack of increased activity observed after specific stimulation with lymphoma cells, nonspecific stimulation of long-term MLTC cells either with supernatants from secondary mixed leukocyte cultures (2 degrees MLC SN) or with supernatants from concanavalin A-stimulated spleen cells leads, on a per cell basis, to a further 5 to 10-fold increase in CTL activity. The stimulatory activity of 2 degrees MLC SN is due to a factor(s) of apparent mol. wt. of 25,000 to 40,000. The activity of the CTL populations formed under these conditions is at least 100-fold higher against syngeneic as compared to allogeneic MLV-induced or unrelated tumor cells.

摘要

先前的研究表明,来自已排斥由莫洛尼肉瘤病毒-白血病病毒(MSV-MLV)复合物诱导的肿瘤的小鼠的淋巴细胞,在混合白细胞-肿瘤细胞培养物(MLTC)中用同基因的、经辐照的MLV诱导的淋巴瘤细胞进行体外刺激后,会产生高水平的特异性H-2限制性细胞毒性T淋巴细胞(CTL)活性。试图通过用同基因的、经辐照的淋巴瘤细胞再次刺激长期MLTC细胞来进一步提高裂解活性,但只取得了有限的成功。本报告表明,与用淋巴瘤细胞进行特异性刺激后观察到的活性缺乏增加相反,用二级混合白细胞培养物(2度MLC SN)的上清液或伴刀豆球蛋白A刺激的脾细胞的上清液对长期MLTC细胞进行非特异性刺激,以每个细胞为基础,会使CTL活性进一步增加5至10倍。2度MLC SN的刺激活性归因于一种表观分子量为25,000至40,000的因子。在这些条件下形成的CTL群体对同基因MLV诱导的或无关肿瘤细胞的活性比对异基因肿瘤细胞的活性至少高100倍。

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