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用白细胞介素-2激活的淋巴细胞对恶性疾病进行过继性免疫治疗。

Adoptive immunotherapy of malignant diseases with IL-2-activated lymphocytes.

作者信息

Kimoto Y, Taguchi T

机构信息

Department of Oncologic Surgery, Osaka University, Japan.

出版信息

Biken J. 1987 Jun;30(2):29-38.

PMID:3501954
Abstract

Lymphokine activated killer cells (LAK cells) or interleukin 2 (IL-2)-activated killer cells were induced by recombinant IL-2 (TGP-3) for clinical adoptive immunotherapy of malignant diseases. After incubation of peripheral blood lymphocytes (PBL) with IL-2 and normal human plasma for 1-2 weeks LAK cells were obtained that showed a maximum cytotoxicity against target cells, and did not need a toxic dose of IL-2 to enhance or maintain their cytotoxicity. Both autologous and allogeneic LAK cells were used in five clinical cases without any immune side effects, and were effective in three cases.

摘要

淋巴因子激活的杀伤细胞(LAK细胞)或白细胞介素2(IL-2)激活的杀伤细胞由重组IL-2(TGP-3)诱导产生,用于恶性疾病的临床过继性免疫治疗。外周血淋巴细胞(PBL)与IL-2和正常人血浆孵育1至2周后,获得的LAK细胞对靶细胞显示出最大细胞毒性,且不需要毒性剂量的IL-2来增强或维持其细胞毒性。在5例临床病例中使用了自体和异体LAK细胞,均未出现任何免疫副作用,其中3例有效。

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