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一类新型肿瘤特异性杀伤细胞的强大抗肿瘤活性。

Potent antitumour activity of a new class of tumour-specific killer cells.

作者信息

Chen S Y, Yang A G, Chen J D, Kute T, King C R, Collier J, Cong Y, Yao C, Huang X F

机构信息

Department of Cancer Biology, Comprehensive Cancer Center, Bowman Gray School of Medicine, Wake Forest University, Winston-Salem, North Carolina 27157, USA.

出版信息

Nature. 1997 Jan 2;385(6611):78-80. doi: 10.1038/385078a0.

Abstract

Two approaches to the antibody-directed targeting of toxic or cytolytic activity and augmentation of cellular immune responses have been explored for tumour immunotherapy, but so far success has been limited. Obstacles facing immunotherapy are the limited accessibility of antibodies or antibody conjugates to solid tumours and the difficulty in obtaining tumour-specific cytotoxic lymphocytes. Here we generate a new class of tumour-specific killer cells by genetically modifying lymphocytes to produce and secrete a targeted toxin against an oncoprotein overexpressed on breast and other tumour cells. The transduced lymphocytes were shown to have potent and selective cytotoxicity to tumours in culture and nude mouse models. The potent in vivo antitumour activity is probably a result of the migration of the lymphocytes to tumours as a targeted toxin carrier, and production and accumulation of the targeted toxins inside tumours as a producer. Our approach, which has features of both antibody-directed and cell-mediated immunotherapy, may have application in a gene therapy context.

摘要

肿瘤免疫治疗中探索了两种将有毒或细胞溶解活性进行抗体导向靶向以及增强细胞免疫反应的方法,但迄今为止,成功有限。免疫治疗面临的障碍是抗体或抗体偶联物难以进入实体肿瘤,以及难以获得肿瘤特异性细胞毒性淋巴细胞。在此,我们通过基因改造淋巴细胞以产生并分泌针对在乳腺及其他肿瘤细胞上过表达的一种癌蛋白的靶向毒素,从而生成了一类新型肿瘤特异性杀伤细胞。在培养模型和裸鼠模型中,转导的淋巴细胞对肿瘤显示出强大且选择性的细胞毒性。体内强大的抗肿瘤活性可能是由于淋巴细胞作为靶向毒素载体迁移至肿瘤,以及作为生产者在肿瘤内部产生并积累靶向毒素的结果。我们的方法兼具抗体导向免疫治疗和细胞介导免疫治疗的特点,可能在基因治疗领域有应用价值。

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