自体和异体淋巴细胞对培养的人肺癌细胞的细胞毒性:产生细胞毒性淋巴细胞的最佳条件。

Gan Pub Date : 1984-11-01
H Kimura, Y Yamaguchi, T Fujisawa
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引用次数: 0

摘要

研究了体外培养抗自体肺癌细胞的细胞毒淋巴细胞的最佳条件。在时间过程实验中,新鲜淋巴细胞对自体肿瘤细胞不表现出任何细胞毒性,但当在T细胞生长因子(IL2)的存在下培养时,淋巴细胞在孵育开始3天后对自体肿瘤细胞具有细胞毒性,并且细胞毒性继续增加,在第7天达到最大值。该研究比较了il - 2和植物血凝素(phytohemagglutinin, PHA)的作用,结果表明,虽然用PHA培养的淋巴细胞确实表现出明显的细胞毒性,但用il - 2培养的淋巴细胞表现出更高的活性。外周血、区域淋巴结(RNL)和远端淋巴结淋巴细胞以及肿瘤浸润淋巴细胞是产生细胞毒性淋巴细胞的来源。在这4种来源中,RNL被证明是最稳定可靠的细胞毒性淋巴细胞来源。自体肿瘤细胞体外刺激的结果是矛盾的。25例肿瘤细胞体外刺激与不刺激的实验结果显示,肿瘤细胞刺激后细胞毒性增强9例(36%),抑制5例,其余无作用。淋巴细胞单克隆抗体鉴定表明,自体肿瘤细胞裂解细胞为OKT3+、OKT8+、OKT4-、OKM1-。
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Cytotoxicity of autologous and allogeneic lymphocytes against cultured human lung cancer cells: optimal conditions for the production of cytotoxic lymphocytes.

Optimal conditions for the in vitro production of cytotoxic lymphocytes against autologous lung cancer cells were studied. In the time-course experiments, fresh lymphocytes did not exhibit any cytotoxicity against autologous tumor cells, but, when cultured in the presence of T cell growth factor (IL2), the lymphocytes became cytotoxic against autologous tumor cells 3 days after the initiation of incubation and the cytotoxicity continued to increase, reaching a maximum at day 7. The study, conducted to compare the effects of IL2 and phytohemagglutinin (PHA), demonstrated that although lymphocytes cultured with PHA did exhibit a significant cytotoxicity, lymphocytes cultured with IL2 showed much higher activity. Peripheral blood, regional lymph node (RNL) and distal lymph node lymphocytes, and tumor infiltrating lymphocytes were tested as sources for the production of cytotoxic lymphocytes. Among these 4 sources, RNL proved the most consistently reliable source of cytotoxic lymphocytes. The results of in vitro stimulation by autologous tumor cells were ambivalent. Twenty-five experiments that compared in vitro stimulation by tumor cells and no stimulation revealed that 9 cases (36%) showed enhancement of cytotoxicity after stimulation with tumor cells, 5 cases showed inhibition, and the remainder no effect. Characterization of lymphocytes by using monoclonal antibodies indicated that cells lytic for autologous tumor cells are OKT3+, OKT8+, OKT4-, OKM1-.

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