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[受体介导的癌症治疗——杀肿瘤细胞因子、LAK和TIL的过继性治疗]

[Receptor-mediated cancer therapy--tumoricidal cytokines, adoptive therapy of LAK, TIL].

作者信息

Niitsu Y, Watanabe N, Kondo H, Kanisawa Y

机构信息

Dept. of Internal Medicine, Sapporo Medical College.

出版信息

Gan To Kagaku Ryoho. 1990 Jun;17(6):1134-41.

PMID:1693487
Abstract

Three modes of receptor-mediated cancer therapy were reviewed presenting our own data. Employment of tumoricidal cytokines (IFN, TNF, LT) to this type of therapy has been expected to be the most promising approach. However, preclinical and clinical results so far obtained, revealed that they were useful only for the very limited diseases including renal cancer or some hematological malignancies. Second approach is to utilize growth factors conjugated with toxin or carzinostatin which are readily internalized into tumor cells. In this context, transferrin-neocarzinostatin was examined in our laboratory both in vitro and in vivo for its anticancer activity and was found to suppress tumor growth more significantly than neocarzinostatin alone on the basis of molar ratio. Thus this approach may be worthy to be clinically investigated. Adoptive therapy of lymphokine activated killer (LAK) or tumor infiltrating lymphocyte (TIL) may also be categorized into receptor mediated cancer treatment since both are activated by signals through IL-2 receptor. Although clinical evaluation is still on going, the therapy appears to be effective only when effector cells are administered locally to tumors.

摘要

我们结合自身数据,对受体介导的三种癌症治疗模式进行了综述。利用杀肿瘤细胞因子(干扰素、肿瘤坏死因子、淋巴毒素)进行此类治疗有望成为最具前景的方法。然而,目前获得的临床前和临床结果表明,它们仅对包括肾癌或某些血液系统恶性肿瘤在内的非常有限的疾病有用。第二种方法是利用与毒素或抑癌素结合的生长因子,这些生长因子很容易被肿瘤细胞内化。在此背景下,我们实验室对转铁蛋白-新制癌菌素的体外和体内抗癌活性进行了研究,发现基于摩尔比,它比单独使用新制癌菌素更能显著抑制肿瘤生长。因此,这种方法可能值得进行临床研究。过继性细胞免疫治疗(淋巴因子激活的杀伤细胞或肿瘤浸润淋巴细胞)也可归类为受体介导的癌症治疗,因为两者均通过白细胞介素-2受体的信号被激活。尽管临床评估仍在进行中,但该疗法似乎仅在将效应细胞局部注射到肿瘤部位时才有效。

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