Augmentation of specific tumor killing activity by tumor-infiltrating lymphocytes (TIL) in the presence of TNF-SAM2.

S Goto, Y Suma, K Noguchi, J Kera, S Sakai, G I Soma, S Takeuchi
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Abstract

The effect of TNF-SAM2 on cytotoxic activity of tumor-infiltrating lymphocytes (TIL) was investigated. TIL were prepared from 11 human cancer patients. They were propagated by double in vitro stimulation with anti-CD3 monoclonal antibody and interleukin-2, and cultured for 3 weeks. The cytotoxic activity of TIL was tested with standard 4h 51Cr-release assays in the presence or the absence of TNF-SAM2. In the presence of TNF-SAM2 (500U/ml), the mean cytotoxic activity against autologous tumor cells was significantly augmented compared to that in its absence. However, the fact that cytotoxic activity against K562 and Daudi showed no difference whether substance was present or not, indicates that LAK and NK activity were not affected by TNF-SAM2. Direct cytotoxicity by exogenously added TNF-SAM2 to tumor cells was measured in 9 out of 11 cases and this revealed that cytotoxicity solely by TNF-SAM2 was seen in 3 tumors. However, there was no correlation between the augmentation of cytotoxicity by TIL in the presence of TNF-SAM2 and the cytotoxicity shown by TNF-SAM2 alone. These results suggested that TIL therapy combined with administration of exogenous TNF may exert a synergistically stronger therapeutic effect on cancer.

肿瘤浸润淋巴细胞(TIL)在TNF-SAM2存在下特异性肿瘤杀伤活性的增强
研究了TNF-SAM2对肿瘤浸润淋巴细胞(TIL)细胞毒活性的影响。TIL取自11例人类癌症患者。用抗cd3单克隆抗体和白细胞介素-2双重体外刺激增殖,培养3周。在TNF-SAM2存在或不存在的情况下,用标准的4h 51cr释放法检测TIL的细胞毒活性。在TNF-SAM2 (500U/ml)存在时,对自体肿瘤细胞的平均细胞毒活性比不存在时显著增强。然而,无论是否存在该物质,对K562和Daudi的细胞毒活性均无差异,这表明TNF-SAM2不影响LAK和NK活性。外源性添加TNF-SAM2对肿瘤细胞的直接细胞毒性在11例中有9例进行了测量,这表明在3例肿瘤中仅观察到TNF-SAM2的细胞毒性。然而,在TNF-SAM2存在的情况下,TIL对细胞毒性的增强与TNF-SAM2单独显示的细胞毒性之间没有相关性。这些结果表明,TIL联合外源性TNF治疗可能对癌症发挥更强的协同治疗作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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