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In vitro activation of natural killer-like cytotoxicity by specifically in vivo primed T-helper lymphocytes in the rat.

机译:大鼠体内特异性体内引发的T辅助淋巴细胞在体外激活天然杀伤样细胞毒性。

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摘要

The interaction between the rat non-cytotoxic T lymphocyte subset, which is marked by the W3/25 monoclonal antibody, and natural killer cells was investigated. Specifically in vivo primed lymph node cells were restimulated in vitro with the priming antigen and co-cultured with a source of natural killer cells and their precursors. Cytotoxic activity, generated during a 4 day incubation period, was assessed by lysis of a rat natural killer cell-sensitive tumour target cell line, y3Ag123. This cytotoxic activity was more fully described as natural killer cell cytotoxicity on the basis of target cell specificity, using a range of natural killer cell-susceptible and -resistant targets. The W3/25-positive T cell, separated from the in vivo primed lymph node cells by nylon wool column elution, antibody labelling and sorting on the fluorescence-activated cell sorter, was shown to be necessary to stimulate the generation of this activity. W3/25-negative cells were not active in this respect. The activation was shown to be mediated via lymphokine(s), probably interleukin-2, present in concanavalin A-induced lymphocyte culture supernatants. These supernatants could be used to substitute for in vivo primed, restimulated W3/25-positive lymph node cells in activating natural killer cell cytotoxicity from normal spleen cells. Nylon wool column-eluted spleen cells, activated in vitro with conditioned medium were separated into OX8-positive and OX8-negative subsets using the fluorescence-activated cell sorter. The distribution of cytotoxic activity related to that of freshly derived rat natural killer cells.
机译:研究了以W3 / 25单克隆抗体为标志的大鼠非细胞毒性T淋巴细胞亚群与自然杀伤细胞之间的相互作用。具体地,用引发抗原在体外对体内引发的淋巴结细胞进行再刺激,并与天然杀伤细胞及其前体来源共培养。通过裂解大鼠自然杀伤细胞敏感的肿瘤靶细胞系y3Ag123评估了在4天的温育期间产生的细胞毒活性。基于靶细胞特异性,使用一系列对自然杀伤细胞敏感和抗性的靶标,这种细胞毒性活性被更充分地描述为自然杀伤细胞的细胞毒性。 W3 / 25阳性T细胞通过尼龙毛柱洗脱,荧光标记的细胞分选仪上的抗体标记和分选与体内启动的淋巴结细胞分离,被证明对刺激这种活性的产生是必需的。 W3 / 25阴性细胞在这方面没有活性。激活被证明是通过伴刀豆球蛋白A诱导的淋巴细胞培养上清液中的淋巴因子(可能是白介素2)介导的。这些上清液可用于替代体内引发的,重新刺激的W3 / 25阳性淋巴结细胞,从而激活正常脾细胞对自然杀伤细胞的细胞毒性。使用荧光激活的细胞分选仪,将在体外用条件培养基激活的尼龙羊毛柱洗脱的脾细胞分为OX8阳性和OX8阴性的子集。细胞毒性活性的分布与新鲜衍生的大鼠自然杀伤细胞的分布有关。

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