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采用粒细胞集落刺激因子(G-CSF)和溶链菌制剂(OK-432)免疫化疗对小鼠Colon26实体瘤进行的治疗

Curative treatments of murine Colon26 solid tumors by immunochemotherapy with G-CSF and OK-432.

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 Apr;29(3):235-43. doi: 10.1016/0162-3109(95)00060-7.

Abstract

In order to study the clinical usefulness of biological response modifiers (BRMs) in eliminating malignant solid tumors, we have investigated the effect of various combination therapies on the murine Colon26 solid tumor model. When the tumor-bearing mice were treated with chemotherapeutics, G-CSF and OK-432 (streptococcal preparation), the tumors completely disappeared from all of the treated mice. When these survivors were rechallenged with Colon26 tumor cells on Day 120, all of them survived without showing any sign of recurrence or metastases. The results indicate that mice with malignant solid tumors, which can not be cured using chemotherapeutics alone, may be completely healed with a combination immuno-chemotherapy. During the course of this combination therapy, study, it was found that there was a clear positive correlation between immunosuppressive acidic protein (IAP) levels and tumor sizes. Suppressor macrophages (sM phi) which produce IAP were found to be decreased in bone marrow and spleen of treated mice. This suggests that the combination therapy may make the mice recover from a suppressed immune state caused by sM phi. In conclusion, the combination therapy with chemotherapeutics and BRMs could cure the solid tumor-bearing mice very effectively through not only synergistic direct tumor cell destruction but also indirect immunomodulation of the host.

摘要

为了研究生物反应调节剂(BRM)在消除恶性实体瘤方面的临床实用性,我们研究了各种联合疗法对小鼠Colon26实体瘤模型的影响。当荷瘤小鼠接受化疗药物、粒细胞集落刺激因子(G-CSF)和溶链菌制剂OK-432治疗时,所有接受治疗的小鼠肿瘤均完全消失。当这些存活小鼠在第120天再次接种Colon26肿瘤细胞时,它们全部存活,未出现任何复发或转移迹象。结果表明,单用化疗药物无法治愈的恶性实体瘤小鼠,可能通过免疫化疗联合疗法完全治愈。在这种联合治疗过程中,研究发现免疫抑制酸性蛋白(IAP)水平与肿瘤大小之间存在明显的正相关。发现产生IAP的抑制性巨噬细胞(sM phi)在治疗小鼠的骨髓和脾脏中减少。这表明联合疗法可能使小鼠从由sM phi引起的免疫抑制状态中恢复。总之,化疗药物与BRM的联合疗法不仅可以通过协同直接破坏肿瘤细胞,还可以通过间接调节宿主免疫,非常有效地治愈荷实体瘤小鼠。

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