Powers Kimberly A, Dixit Narendra M, Ribeiro Ruy M, Golia Preeti, Talal Andrew H, Perelson Alan S
Theoretical Biology and Biophysics, Los Alamos National Laboratory, Los Alamos, New Mexico 87545, USA.
Semin Liver Dis. 2003;23 Suppl 1:13-8. doi: 10.1055/s-2003-41630.
Administration of peginterferon alfa-2b plus ribavirin results in an early hepatitis C virus (HCV) RNA decay followed by an increase as the drug concentration declines between doses. Upon administration of the next dose 1 week later, the same pattern is observed. We have incorporated pharmacokinetic/pharmacodynamic analysis into a model of viral dynamics to describe the effect that changes in drug concentration and effectiveness can have on viral levels. To illustrate the relationship between pharmacokinetics and viral dynamics, we fit the model to data from four HCV/human immunodeficiency virus co-infected patients, and obtained good agreement with the measured serum HCV RNA levels. We were able to account for the observed increases in HCV RNA, and estimate virion and drug half-lives that are in agreement with previous reports. Models incorporating pharmacokinetics are needed to correctly interpret viral load changes and estimate drug effectiveness in treatment protocols using peginterferon alfa-2b.
聚乙二醇干扰素α-2b联合利巴韦林治疗会导致丙型肝炎病毒(HCV)RNA早期衰减,随后随着剂量间药物浓度下降而增加。在1周后给予下一剂药物时,会观察到相同的模式。我们已将药代动力学/药效学分析纳入病毒动力学模型,以描述药物浓度和有效性变化对病毒水平的影响。为了说明药代动力学与病毒动力学之间的关系,我们将该模型与4例HCV/人类免疫缺陷病毒合并感染患者的数据进行拟合,得到了与实测血清HCV RNA水平的良好一致性。我们能够解释观察到的HCV RNA增加情况,并估计与先前报道一致的病毒体和药物半衰期。需要纳入药代动力学的模型来正确解释病毒载量变化,并在使用聚乙二醇干扰素α-2b的治疗方案中估计药物有效性。