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Mathematical modeling based on lamivudine switching to adefovir dipivoxil and to entecavir anti-hepatitis B infection treatment

机译:基于拉米夫鲁德切换到Adefovir Dipivoxil的数学建模和entecavir抗乙型肝炎感染治疗方法

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Lamivudine (LVD) is one of the popular drugs to be used for anti-hepatitis B virus infection therapy. About 39% HBeAg-positive chronic hepatitis B (CHB) patients can achieve serum hepatitis B virus (HBV) DNAs below the low limit of test after one years' treatment. However the antiviral-resistance HBV mutation to LVD treatment is near 60% after three year's therapy. Combination treatment is one method to such kind patients. Based on a LVD mutation (YMDD mutation) CHB patient's clinic data and our improved basic virus infection model, this paper introduces a mathematical model whose parameters change according to different therapy periods. Numerical simulations show that the simulated HBV DNA levels are in good agreement with the HBV DNA evolution of the patient's therapy for switching lamivudine (LVD) + placebo to adefovir dipivoxil (AD) and then to entecavir (EV). The model predicts that it needs about 9 years to clean the patient's all infected liver cells if the patient's immune functions can be kept after the therapy.
机译:拉米夫定(LVD)是用于抗乙型肝炎病毒感染治疗的流行药物之一。约39%的HBEAG阳性慢性乙型肝炎(CHB)患者可以在一年后达到低于试验的低限制的血清乙型肝炎病毒(HBV)DNA。然而,三年治疗后,抗病毒性HBV突变对LVD治疗接近60%。组合治疗是这种患者的一种方法。基于LVD突变(YMDD突变)CHB患者的诊所数据和我们改进的基本病毒感染模型,本文介绍了一种数学模型,其参数根据不同的治疗期改变。数值模拟表明,模拟的HBV DNA水平与患者治疗的HBV DNA演变与切换拉米夫定(LVD)+安慰剂转换为Adefovir Dipivoxil(AD),然后转到Entecavir(EV)。该模型预测,如果患者的免疫功能在治疗后可以保留患者的免疫功能,它需要大约9年才能清洁患者的所有感染的肝细胞。

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