环磷酰胺
医学
肿瘤浸润淋巴细胞
过继性细胞移植
免疫疗法
过继免疫治疗
淋巴因子激活杀伤细胞
癌症研究
癌症
免疫学
白细胞介素2
腺癌
免疫系统
T细胞
化疗
内科学
白细胞介素21
作者
Steven A. Rosenberg,Paul J. Spiess,René Lafrenière
出处
期刊:Science
[American Association for the Advancement of Science]
日期:1986-09-19
卷期号:233 (4770): 1318-1321
被引量:1807
标识
DOI:10.1126/science.3489291
摘要
The adoptive transfer of tumor-infiltrating lymphocytes (TIL) expanded in interleukin-2 (IL-2) to mice bearing micrometastases from various types of tumors showed that TIL are 50 to 100 times more effective in their therapeutic potency than are lymphokine-activated killer (LAK) cells. Therefore the use of TIL was explored for the treatment of mice with large pulmonary and hepatic metastatic tumors that do not respond to LAK cell therapy. Although treatment of animals with TIL alone or cyclophosphamide alone had little impact, these two modalities together mediated the elimination of large metastatic cancer deposits in the liver and lung. The combination of TIL and cyclophosphamide was further potentiated by the simultaneous administration of IL-2. With the combination of cyclophosphamide, TIL, and IL-2, 100% of mice ( n = 12) bearing the MC-38 colon adenocarcinoma were cured of advanced hepatic metastases, and up to 50% of mice were cured of advanced pulmonary metastases. Techniques have been developed to isolate TIL from human tumors. These experiments provide a rationale for the use of TIL in the treatment of humans with advanced cancer.
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