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通过自体混合淋巴细胞肿瘤细胞培养与T细胞生长因子产生针对自体实体瘤的人细胞毒性T淋巴细胞。

Generation of human cytotoxic T lymphocytes against autologous solid tumors by autologous mixed lymphocyte tumor cell culture with T cell growth factor.

作者信息

Ichino Y, Ishikawa T

出版信息

Auris Nasus Larynx. 1985;12 Suppl 2:S226-33. doi: 10.1016/s0385-8146(85)80064-x.

Abstract

Autologous mixed lymphocyte tumor cell cultures (MLTC) generated cytotoxicity against autologous tumors in 5 out of 15 (33%) patients with head and neck cancer. Further cultivation of MLTC-activated lymphocytes with T cell growth factor (TCGF) resulted not only in the propagation of cytotoxic T lymphocytes (CTL) and an increase of cytotoxicity against autologous tumors, but also in the induction of killer cells against allogeneic tumor cells. The results of crisscross tests using fresh tumor cells from 17 donors and lymphocytes from 10 donors indicate that cultivation of MLTC-activated lymphocytes with TCGF generated killer cells cytotoxic for allogeneic tumors in most cases, but not for autologous or allogeneic phytohemagglutinin-induced lymphoblasts. Further, the results of a cold target inhibition test undertaken in an autologous tumor killing system suggest that at least 2 different subsets, specifically cytotoxic for autologous tumors and cytotoxic for both autologous and allogeneic tumors, were developed in the CTL induced by autologous MLTC followed by cultivation with TCGF. The phenotypes of the effector cells were shown to be OKT3+, Leu2a+, OKT8+, OKM1-, and Leu7- by blocking assay using complement and monoclonal antibody against the T cell surface marker.

摘要

在15例头颈癌患者中,有5例(33%)的自体混合淋巴细胞肿瘤细胞培养物(MLTC)对自体肿瘤产生了细胞毒性。用T细胞生长因子(TCGF)进一步培养MLTC激活的淋巴细胞,不仅导致细胞毒性T淋巴细胞(CTL)增殖,对自体肿瘤的细胞毒性增加,还诱导出针对同种异体肿瘤细胞的杀伤细胞。使用来自17名供体的新鲜肿瘤细胞和来自10名供体的淋巴细胞进行的交叉试验结果表明,用TCGF培养MLTC激活的淋巴细胞在大多数情况下产生了对同种异体肿瘤具有细胞毒性的杀伤细胞,但对自体或同种异体植物血凝素诱导的淋巴母细胞则没有。此外,在自体肿瘤杀伤系统中进行的冷靶抑制试验结果表明,在自体MLTC诱导并用TCGF培养后产生的CTL中,至少形成了2个不同的亚群,分别对自体肿瘤具有特异性细胞毒性以及对自体和同种异体肿瘤均具有细胞毒性。通过使用补体和针对T细胞表面标志物的单克隆抗体进行阻断试验,效应细胞的表型显示为OKT3 +、Leu2a +、OKT8 +、OKM1 -和Leu7 -。

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