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术前免疫化疗对小鼠MM48肿瘤淋巴结转移的抑制作用。

The inhibitory effect of preoperative immunochemotherapy on the lymph node metastasis of murine MM48 tumor.

作者信息

Kudo C, Saito M, Yoshida T

机构信息

Central Research Laboratories, Chugai Pharmaceutical Co., Ltd., Tokyo, Japan.

出版信息

Immunopharmacology. 1995 Aug;30(2):139-46. doi: 10.1016/0162-3109(95)00015-l.

Abstract

A murine tumor model showing metastases to lymph nodes (LN) was established by intradermally implanting highly metastatic MM48 tumor cells (2 x 10(6)) in C3H/HeN mice. We were searching for the most effective immunochemotherapeutic modality to treat this metastatic tumor. The combination therapy with chemotherapeutics, granulocyte colony-stimulating factor (G-CSF) and OK-432 on Days 8-11 was found to be remarkably effective, making the solid tumor disappear in more than half of the treated mice, though all of them eventually died of LN metastasis, as all the control mice did. Then an attempt was made to cure the mice from such fatal metastatic tumors with combined immunochemotherapy prior to surgical resection on Day 14. The combination therapy with chemotherapeutics, G-CSF and OK-432 more strongly inhibited the metastases then, and more than 85% of the mice survived. When the survivors were rechallenged with MM48 tumor cells, all of them rejected and survived without recurrences and metastases, indicating the acquirement of specific immunity. It is expected that this preoperative immunochemotherapy may be clinically useful for the treatment of malignant neoplasms.

摘要

通过在C3H/HeN小鼠皮内植入高转移性MM48肿瘤细胞(2×10⁶个)建立了一种显示有淋巴结转移的小鼠肿瘤模型。我们在寻找治疗这种转移性肿瘤的最有效免疫化学治疗方法。结果发现,在第8至11天联合使用化疗药物、粒细胞集落刺激因子(G-CSF)和OK-432进行治疗非常有效,超过一半的受试小鼠体内实体瘤消失,不过它们最终都像所有对照小鼠一样死于淋巴结转移。然后尝试在第14天手术切除前通过联合免疫化学疗法治愈患有这种致命转移性肿瘤的小鼠。那时,化疗药物、G-CSF和OK-432的联合治疗对转移的抑制作用更强,超过85%的小鼠存活下来。当对存活小鼠再次接种MM48肿瘤细胞时,所有小鼠都将其排斥并存活下来,没有复发和转移,这表明获得了特异性免疫。预计这种术前免疫化学疗法可能在临床上对恶性肿瘤的治疗有用。

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