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TP - 3(精氨酸 - 赖氨酸 - 天冬氨酸)、TP - 4(精氨酸 - 赖氨酸 - 天冬氨酸 - 缬氨酸)和TP - 5对静脉注射的Lewis肺癌细胞转移能力的影响。

The effect of TP-3 (Arg-Lys-Asp), TP-4 (Arg-Lys-Asp-Val), and TP-5 on the metastatic capacity of intravenously injected Lewis lung tumor cells.

作者信息

Szende B, Lapis K, Pal K, Sipos L, Denes L, Kisfaludy L

机构信息

First Institute of Pathology and Experimental Cancer Research of Semmelweis Medical University, Budapest, Hungary.

出版信息

Immunopharmacol Immunotoxicol. 1987;9(1):19-24. doi: 10.3109/08923978709035199.

Abstract

The oligopeptides Arg-Lys-Asp (TP-3), Arg-Lys-Asp-Val (TP-4), and Arg-Lys-Asp-Val-Tyr (TP-5) considered as the active short fragments of thymopoietin were administered (lo mg/kg) to C57B1 mice 24 hours before the intravenous inoculation of Lewis lung tumor (LLT) cells. A substantial decrease in lung metastasis number was observed as a result of treatment with all of the three oligopeptides. TP-3, TP-4, and TP-5 treatment decreased the immunosuppressive activity of Cyclophosphamid (240 mg/kg) given 96 hours before the inoculation of LLT cells. After thymectomy, performed eight days before the LLT inoculation, only TP-3 treatment resulted in the decrease of Cyclophosphamid immunotoxicity. A stimulating effect of TP-3 on T helper cell activity is assumed. The oligopeptides TP-3, TP-4, and TP-5 are recommended for clinical trial in case of malignant tumors and immunodeficiency.

摘要

将被视为胸腺生成素活性短片段的寡肽精氨酸-赖氨酸-天冬氨酸(TP-3)、精氨酸-赖氨酸-天冬氨酸-缬氨酸(TP-4)和精氨酸-赖氨酸-天冬氨酸-缬氨酸-酪氨酸(TP-5)(10毫克/千克)在静脉接种Lewis肺癌(LLT)细胞前24小时给予C57B1小鼠。用这三种寡肽中的任何一种进行治疗后,均观察到肺转移数量大幅减少。TP-3、TP-4和TP-5治疗降低了在接种LLT细胞前96小时给予的环磷酰胺(240毫克/千克)的免疫抑制活性。在接种LLT细胞前八天进行胸腺切除术后,只有TP-3治疗导致环磷酰胺免疫毒性降低。推测TP-3对辅助性T细胞活性有刺激作用。推荐将寡肽TP-3、TP-4和TP-5用于恶性肿瘤和免疫缺陷患者的临床试验。

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