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人脑肿瘤细胞介导免疫反应的体外研究。I. 诱导对同种异体培养神经胶质瘤细胞介导的细胞毒性反应中第三方刺激淋巴细胞的需求。

In vitro studies on the cell-mediated immune response to human brain tumors. I. Requirement for third-party stimulator lymphocytes in the induction of cell-mediated cytotoxic responses to allogeneic cultured gliomas.

作者信息

Gately M K, Glaser M, Dick S J, Mettetal R W, Kornblith P L

出版信息

J Natl Cancer Inst. 1982 Dec;69(6):1245-54.

PMID:6183477
Abstract

For study of those properties of human gliomas that might contribute to their ability to escape cell-mediated immune attack, cultured human glioma cells were examined for their ability to elicit allogeneic cytolytic lymphocyte responses in vitro. Of 9 glioma lines, 5 were unable to elicit allogeneic cytolytic lymphocyte responses in mixed lymphocyte--tumor cultures although the concentration of stimulating glioma cells was varied over a fortyfold range. However, lymphocytes specifically cytolytic for 4 of the nonstimulatory lines could be generated if irradiated, third-party stimulator lymphocytes were added to cultures containing responder lymphocytes and glioma cells. The specific cytolytic lymphocytes produced in these cultures were inactivated by treatment with the monoclonal anti-T-cell antibody OKT3 plus complement and were thus identified as T-cells. However, nonspecific, non-T-lytic effectors were also generated. The results of these experiments demonstrated that certain cultured gliomas possessed a defect in immunogenicity that can be overcome by "help" from an allogeneic mixed lymphocyte reaction. The possible nature of this help and the potential implications of these results for the immunotherapy of human gliomas are discussed.

摘要

为了研究人类胶质瘤的那些可能有助于其逃避细胞介导免疫攻击的特性,检测了培养的人类胶质瘤细胞在体外引发同种异体溶细胞淋巴细胞反应的能力。在9个胶质瘤细胞系中,5个在混合淋巴细胞-肿瘤培养物中无法引发同种异体溶细胞淋巴细胞反应,尽管刺激胶质瘤细胞的浓度在40倍范围内变化。然而,如果将经辐照的第三方刺激淋巴细胞添加到含有反应淋巴细胞和胶质瘤细胞的培养物中,就可以产生对4个无刺激作用的细胞系具有特异性溶细胞作用的淋巴细胞。这些培养物中产生的特异性溶细胞淋巴细胞经单克隆抗T细胞抗体OKT3加补体处理后失活,因此被鉴定为T细胞。然而,也产生了非特异性的非T细胞溶解效应细胞。这些实验结果表明,某些培养的胶质瘤具有免疫原性缺陷,这种缺陷可以通过同种异体混合淋巴细胞反应的“辅助”来克服。本文讨论了这种辅助的可能性质以及这些结果对人类胶质瘤免疫治疗的潜在意义。

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