Itoh Y, Koshita Y, Takahashi M, Watanabe N, Kohgo Y, Niitsu Y
Fourth Department of Internal Medicine, Sapporo Medical University School of Medicine, Japan.
Cancer Immunol Immunother. 1995 Feb;40(2):95-102. doi: 10.1007/BF01520290.
We characterized tumor-infiltrating lymphocytes (TIL) from ascites of patients with ovarian or pancreatic cancer in which the human tumor necrosis factor (TNF) gene was successfully transduced with retrovirus vector. The TNF-gene-transduced TIL (TNF-TIL) from these patients showed a higher level of TNF production and higher cytotoxic activity against K562 and Daudi cells than did neomycin-phosphotransferase-gene-transduced TIL (neo-TIL). Of these TIL preparations, only that from pancreatic cancer was further characterized since it was collected in a relatively large amount. In spite of the fact that the autologous tumor cells showed resistance to soluble TNF, the TNF-TIL clearly demonstrated enhanced cytotoxicity against them as compared with neo-TIL. The enhanced cytotoxicity was ascribed to autocrine effects of secreted TNF on TIL, which included augmentation of adhesion molecule (CD2 and CD11a) and interleukin-2 receptor expression, and elevation of production of interferon gamma, lymphotoxin and granulocyte/macrophage-colony-stimulating factor and its paracrine effect on target cells to facilitate them to be more susceptible to TIL.
我们对来自卵巢癌或胰腺癌患者腹水中的肿瘤浸润淋巴细胞(TIL)进行了特征分析,这些患者的人肿瘤坏死因子(TNF)基因已成功用逆转录病毒载体转导。与新霉素磷酸转移酶基因转导的TIL(neo-TIL)相比,这些患者的TNF基因转导的TIL(TNF-TIL)表现出更高水平的TNF产生以及对K562和Daudi细胞更高的细胞毒性活性。在这些TIL制剂中,只有来自胰腺癌的制剂因其收集量相对较大而得到进一步特征分析。尽管自体肿瘤细胞对可溶性TNF具有抗性,但与neo-TIL相比,TNF-TIL对它们的细胞毒性明显增强。细胞毒性增强归因于分泌的TNF对TIL的自分泌作用,这包括粘附分子(CD2和CD11a)和白细胞介素-2受体表达的增强,以及干扰素γ、淋巴毒素和粒细胞/巨噬细胞集落刺激因子产生的增加及其对靶细胞的旁分泌作用,使它们更容易受到TIL的攻击。