Overgaard Rune V, Karlsson Mats, Ingwersen Steen H
Informatics and Mathematical Modelling, Technical University of Denmark, Richard Petersens Plads, Building 321, Room 015, Lyngby 2800, Denmark.
J Pharmacokinet Pharmacodyn. 2007 Aug;34(4):559-74. doi: 10.1007/s10928-007-9059-z. Epub 2007 May 22.
Interleukin-21 (IL-21) is a novel cytokine that is currently under clinical investigations as a potential anti-cancer agent. Like many other anti-cancer agents, including other interleukins, IL-21 is seen to produce a broad range of biological effects that may be related to both efficacy and safety of treatment. The present analysis investigates the observed pharmacodynamics effects on red blood cells following various treatment schedules of human IL-21 administrated to cynomolgus monkeys. These effects are described by a novel non-linear mixed-effects model that enabled separation of drug effects and sampling effects, the latter believed to be due partly to blood loss and partly to stress induced haemolysis in connection with blood sampling. Two different studies with a total of 9 different treatment groups of cynomolgus monkeys were used for model development. In conclusion, the model describes the IL-21 induced drop in red blood cells to be (1) caused by removal rather than suppression of production, consistent with increased reticulocyte concentration, and (2) considerably delayed compared to dosing, i.e. not related to the drop in red blood cells observed immediately post dose. It is believed that the structural model presented here can be used for other types of drug induced loss of red blood cells, whereas the mechanism for sampling related blood loss is relevant for investigations of anaemia in all pharmacological studies with smaller animals.
白细胞介素-21(IL-21)是一种新型细胞因子,目前正作为一种潜在的抗癌药物进行临床研究。与许多其他抗癌药物一样,包括其他白细胞介素,IL-21被认为会产生广泛的生物学效应,这些效应可能与治疗的有效性和安全性都有关。本分析研究了将人IL-21以不同治疗方案给予食蟹猴后,对红细胞观察到的药效学效应。这些效应由一个新型的非线性混合效应模型来描述,该模型能够区分药物效应和采样效应,后者被认为部分是由于失血,部分是由于与采血相关的应激诱导的溶血。两项不同的研究,共9个不同治疗组的食蟹猴被用于模型开发。总之,该模型描述IL-21诱导的红细胞下降是(1)由清除而非抑制生成引起的,这与网织红细胞浓度增加一致,并且(2)与给药相比有相当大的延迟,即与给药后立即观察到的红细胞下降无关。据信,这里提出的结构模型可用于其他类型药物诱导的红细胞损失,而与采样相关的失血机制与所有使用较小动物的药理学研究中的贫血调查相关。