首页> 外文会议>Modelling, simulation, and identification >DYNAMICS MODELLING OF SWITCHING ADEFOVIR DIPIVOXIL TO ENTECAVIR ANTI-HBV INFECTION PERSONALIZED THERAPY
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DYNAMICS MODELLING OF SWITCHING ADEFOVIR DIPIVOXIL TO ENTECAVIR ANTI-HBV INFECTION PERSONALIZED THERAPY

机译:切换用阿地福韦酯对乙肝病毒感染的个性化治疗的动力学模型

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Adefovir dipivoxil (AD) is a potent inhibitor of hepatitis B virus (HBV). There are over 50% HBeAg-positive chronic hepatitis B (CHB) patients who respond the AD therapy. However clinical remission (low HBV DNA and Normal ALT) in 60% of patients who discontinued adefovir after 4~5 years.rnThe aim of this study was to observe the efficacy of a patient's therapy for switching AD to Entecavir (EV), and modeling the viral dynamics. Based on a patient's AD and EV therapy clinic serum HBV DNA data, we propose an anti-HBV therapy dynamic model, and determine the model parameters.rnThe numerical simulations of the model show that the calculated HBV DNA levels are agreement with in the patient's clinic serum HBV DNA data. The model predicts that if the patient's immune ability can be kept as the same as that in 172 weeks' follow up, the therapy benefit can continue, and all infected cells will be replaced by normal ones after 13.5 years.
机译:阿德福韦酯(AD)是有效的乙型肝炎病毒(HBV)抑制剂。有超过50%的HBeAg阳性慢性乙型肝炎(CHB)患者对AD治疗有反应。然而,在4〜5年后停用阿德福韦的患者中有60%的患者临床缓解(低HBV DNA和正常ALT).rn本研究的目的是观察患者将AD转换为Entecavir(EV)的治疗效果并进行建模病毒动力学。基于患者的AD和EV治疗诊所的血清HBV DNA数据,我们提出了抗HBV治疗的动力学模型,并确定了模型参数.rn该模型的数值模拟表明,计算出的HBV DNA水平与患者的诊所相符血清HBV DNA数据。该模型预测,如果患者的免疫能力能够保持与172周的随访结果相同,则治疗益处可以继续,并且所有感染的细胞将在13.5年后被正常细胞替代。

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