Interleukin-6 induction by a muramyltripeptide derivative in cancer patients.

H Frost, J L Murray, H A Chaudri, J Van Damme
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引用次数: 0

Abstract

Interleukin-6 (IL-6) was measured in sera from 26 patients with advanced malignancies before and after an I.V. infusion of muramyltripeptide-phosphatidylethanolamine (MPT-PE) in liposomes. Significantly elevated IL-6 could be measured 2 and 4 h after medium (0.25-0.5 mg/m2) and high (1.0-6.0 mg/m2) doses of the drug accompanied by a rise in body temperature. The biological activity of IL-6 in sera could be inhibited in vitro by monoclonal antibodies against IL-6. Other biological effects of MTP-PE in vivo such as leukocytosis and elevated acute phase reactants are discussed in view of increased IL-6 levels. It is concluded that MTP-PE in liposomes generates increased amounts of IL-6 measurable in serum several hours after administration. IL-6 could therefore play an important role in the biological response modification induced by the drug.

一种鼠三肽衍生物在癌症患者中诱导白介素-6。
研究了26例晚期恶性肿瘤患者在静脉滴注脂质体中鼠三肽-磷脂酰乙醇胺(MPT-PE)前后血清中白细胞介素-6 (IL-6)的含量。中剂量(0.25 ~ 0.5 mg/m2)和高剂量(1.0 ~ 6.0 mg/m2)用药后2和4 h, IL-6显著升高,同时体温升高。体外抗IL-6单克隆抗体可抑制血清中IL-6的生物活性。鉴于IL-6水平的升高,讨论了MTP-PE在体内的其他生物学效应,如白细胞增多和急性期反应物升高。由此可见,给药数小时后,脂质体中的MTP-PE可使血清中IL-6含量升高。因此,IL-6可能在药物诱导的生物反应修饰中发挥重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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