Toxicity of polyinosinic-polycytidylic acid admixed with poly-L-lysine and solubilized with carboxymethylcellulose in mice.

D Hartmann, M A Schneider, B F Lenz, J E Talmadge
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引用次数: 17

Abstract

Polyinosinic-polycytidylic acid [poly(I,C)] is a double-stranded RNA that is a potent interferon (IFN) inducer in rodents and, when suitably complexed with poly-L-lysine and carboxymethylcellulose [poly(I,C)-LC], also in primates and humans. In addition, poly(I,C)-LC has shown significant therapeutic activity in a number of preclinical tumor models and significant toxicity in both the preclinical and clinical settings. To better understand the toxicity of this agent, particularly in light of the previously reported bell-shaped dose response curve for immunomodulation and therapeutic activity, we undertook a pharmacological/toxicological study of poly(I,C)-LC. These experiments revealed that the injection of toxic doses of poly(I,C)-LC significantly reduced the body weight of animals and induced serological and histological abnormalities. We found that poly(I,C) is the toxic moiety of poly(I,C)-LC and that both agents induced pulmonary thrombosis as well as hepatic necrosis. The hepatic necrosis was reflected in serum enzyme levels, with significant increases in ornithine carbonyl transferase, serum glutamic oxaloacetic transaminase and serum glutamic pyruvic transaminase levels. In addition, reduced platelet counts indicated a significant increase in platelet consumption in agreement with the thrombosis. There were, however, only minor changes in prothrombin and activated prothrombin times. It was of interest that coincubating poly(I,C)-LC and peritoneal macrophages in vitro resulted in the production of tumor necrosis factor, which has a similar pattern of toxicity; this finding suggests that poly(I,C)-LC's pattern of toxicity may be associated with the induction of TNF and/or IFN.

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聚肌酸-多胞酸与聚赖氨酸混合并与羧甲基纤维素溶解对小鼠的毒性。
聚肌苷-多胞酸[poly(I,C)]是一种双链RNA,在啮齿类动物中是一种有效的干扰素(IFN)诱导剂,当与聚l -赖氨酸和羧甲基纤维素[poly(I,C)-LC]适当配合时,也适用于灵长类动物和人类。此外,poly(I,C)-LC在许多临床前肿瘤模型中显示出显著的治疗活性,在临床前和临床环境中均显示出显著的毒性。为了更好地了解这种药物的毒性,特别是考虑到先前报道的钟形剂量反应曲线对免疫调节和治疗活性的影响,我们对poly(I,C)-LC进行了药理学/毒理学研究。这些实验表明,注射有毒剂量的聚(I,C)-LC可显著降低动物体重,并引起血清学和组织学异常。我们发现poly(I,C)是poly(I,C)-LC的毒性部分,两种药物均可诱导肺血栓形成和肝坏死。肝坏死反映在血清酶水平上,鸟氨酸羰基转移酶、血清谷草酰转氨酶和血清谷丙转氨酶水平显著升高。此外,血小板计数减少表明血小板消耗显著增加,与血栓形成一致。然而,凝血酶原和活化凝血酶原时间只有微小的变化。有趣的是,聚(I,C)-LC与腹腔巨噬细胞体外共孵育可产生肿瘤坏死因子,其毒性模式相似;这一发现表明poly(I,C)-LC的毒性模式可能与TNF和/或IFN的诱导有关。
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