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单克隆抗体首剂细胞因子释放综合征——机制与预测

Monoclonal antibody first dose cytokine release syndromes-mechanisms and prediction.

作者信息

Wing Mark

机构信息

Huntingdon Life Sciences Ltd, Huntingdon, United Kingdom.

出版信息

J Immunotoxicol. 2008 Jan;5(1):11-5. doi: 10.1080/15476910801897433.

Abstract

Acute cytokine release syndromes are associated with some therapeutic antibodies in man, leading to a spectrum of clinical signs from nausea, chills and fever to more serious dose limiting hypotension and tachycardia. When anticipated this syndrome is typically manageable, however this adverse reaction recently became headline news when a massive and unexpected cytokine release syndrome occurred within a few hours of dosing six healthy volunteers with a therapeutic antibody, putting their lives at risk due to multiple organ failure. Preclinical studies did not predict this adverse event, emphasising the need to compare the relative potency of the product in man and the chosen toxicology species, so that additional margins of safety can be applied when conducting first in man (FIM) studies if there is uncertainty over the predictability of the toxicology species. In vitro human PBMC and whole blood cultures may be useful for predicting cytokine release. However since cytokine release arises through at least two distinct mechanisms, it should be emphasised that the utility of these in vitro methods needs to be established for each antibody product.

摘要

急性细胞因子释放综合征与人使用的一些治疗性抗体相关,可导致一系列临床症状,从恶心、寒战和发热到更严重的剂量限制性低血压和心动过速。当预期到这种综合征时,通常是可控的,然而,当给六名健康志愿者注射一种治疗性抗体后数小时内发生了大规模且意外的细胞因子释放综合征,导致他们因多器官衰竭而生命垂危,这一不良反应最近成为了头条新闻。临床前研究并未预测到这一不良事件,这强调了比较产品在人体和所选毒理学物种中的相对效力的必要性,以便在毒理学物种的可预测性存在不确定性时,在进行首次人体研究(FIM)时能够应用额外的安全边际。体外人外周血单核细胞(PBMC)和全血培养可能有助于预测细胞因子释放。然而,由于细胞因子释放至少通过两种不同机制产生,因此应强调,需要针对每种抗体产品确定这些体外方法的实用性。

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