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[自体肿瘤细胞刺激的淋巴因子激活杀伤细胞支气管动脉灌注]

[Bronchial arterial infusion of lymphokine-activated killer cells stimulated by autologous tumor cells].

作者信息

Kimura H, Yamaguchi Y, Obata S, Yusa T, Sekine Y

机构信息

Dept. of Surgery, School of Medicine, Chiba University.

出版信息

Gan To Kagaku Ryoho. 1988 Aug;15(8 Pt 2):2401-4.

PMID:3137876
Abstract

Bronchial arterial infusion (BAI) of Lymphokine activated killer (LAK) cells, stimulated in vitro by autologous tumor cells, was performed for a primary lung cancer patient, a 47-year-old male patient with primary squamous cell carcinoma of the lung who underwent probe thoracotomy and had part of the tumor tissue removed. Peripheral blood lymphocytes were cultured in 500 U/ml of recombinant IL-2(Shionogi Pharm. S6820) for 9 days after in vitro stimulation with mitomycin C-treated primary tumor cells for 3 days. These cells (designated St-LAK cells) were inoculated from the bronchial artery of patients who received 60 Gy irradiation of the primary site and mediastinal lymph nodes. The tumor regressed significantly from 8 X 7 to 3 X 2.5 cm in diameter. The advantages of LAK-BAI using St-LAK cells with irradiation were discussed.

摘要

对一名原发性肺癌患者进行了支气管动脉灌注(BAI),该患者为47岁男性,患有原发性肺鳞状细胞癌,接受了胸腔镜探查并切除了部分肿瘤组织。外周血淋巴细胞在体外经丝裂霉素C处理的原发性肿瘤细胞刺激3天后,于500 U/ml的重组白细胞介素-2(盐野义制药S6820)中培养9天。这些细胞(称为St-LAK细胞)从接受了原发部位和纵隔淋巴结60 Gy照射的患者支气管动脉注入。肿瘤直径从8×7厘米显著缩小至3×2.5厘米。讨论了使用经照射的St-LAK细胞进行LAK-BAI的优势。

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