首页> 外文OA文献 >Antiviral Effects of Lamivudine, Emtricitabine, Adefovir Dipivoxil, and Tenofovir Disoproxil Fumarate Administered Orally Alone and in Combination to Woodchucks with Chronic Woodchuck Hepatitis Virus Infection ▿
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Antiviral Effects of Lamivudine, Emtricitabine, Adefovir Dipivoxil, and Tenofovir Disoproxil Fumarate Administered Orally Alone and in Combination to Woodchucks with Chronic Woodchuck Hepatitis Virus Infection ▿

机译:拉米夫定,恩曲他滨,阿德福韦酯/富马酸替诺福韦酯富马酸酯的抗病毒作用单独和与慢性土拨鼠肝炎肝炎病毒感染的土拨鼠联合使用▿

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摘要

Adefovir dipivoxil (ADV) and tenofovir disoproxil fumarate (TDF) are nucleotide analogs that inhibit the replication of wild-type hepatitis B virus (HBV) and lamivudine (3TC)-resistant virus in HBV-infected patients, including those who are coinfected with human immunodeficiency virus. The combination of ADV or TDF with other nucleoside analogs is a proposed strategy for managing antiviral drug resistance during the treatment of chronic HBV infection. The antiviral effect of oral ADV or TDF, alone or in combination with 3TC or emtricitabine (FTC), against chronic woodchuck hepatitis virus (WHV) infection was evaluated in a placebo-controlled study in the woodchuck, an established and predictive model for antiviral therapy. Once-daily treatment for 48 weeks with ADV plus 3TC or TDF plus FTC significantly reduced serum WHV viremia levels from the pretreatment level by 6.2 log10 and 6.1 log10 genome equivalents/ml serum, respectively, followed by TDF plus 3TC (5.6 log10 genome equivalents/ml), ADV alone (4.8 log10 genome equivalents/ml), ADV plus FTC (one survivor) (4.4 log10 genome equivalents/ml), TDF alone (2.9 log10 genome equivalents/ml), 3TC alone (2.7 log10 genome equivalents/ml), and FTC alone (2.0 log10 genome equivalents/ml). Individual woodchucks across all treatment groups also demonstrated pronounced declines in serum WHV surface antigen, characteristically accompanied by declines in hepatic WHV replication and the hepatic expression of WHV antigens. Most woodchucks had prompt recrudescence of WHV replication after drug withdrawal, but individual woodchucks across treatment groups had sustained effects. No signs of toxicity were observed for any of the drugs or drug combinations administered. In conclusion, the oral administration of 3TC, FTC, ADV, and TDF alone and in combination was safe and effective in the woodchuck model of HBV infection.
机译:阿德福韦酯(ADV)和替诺福韦富马酸二甲酚(TDF)是核苷酸类似物,可抑制HBV感染患者(包括那些与人类共同感染的患者)中抗野生型乙型肝炎病毒(HBV)和拉米夫定(3TC)的病毒的复制免疫缺陷病毒。 ADV或TDF与其他核苷类似物的组合是在慢性HBV感染治疗期间管理抗病毒药物耐药性的拟议策略。在土拨鼠的安慰剂对照研究中评估了口服ADV或TDF单独或与3TC或恩曲他滨(FTC)联合使用对慢性土拨鼠肝炎病毒(WHV)感染的抗病毒作用,该研究是建立和预测的抗病毒治疗模型。每天一次使用ADV加3TC或TDF加FTC进行48周治疗,分别使血清WHV病毒血症水平比治疗前水平分别降低6.2 log10和6.1 log10基因组当量/毫升血清,其次是TDF加3TC(5.6 log10基因组当量/毫升ml),仅ADV(4.8 log10基因组当量/ ml),ADV加FTC(一个幸存者)(4.4 log10基因组当量/ ml),仅TDF(2.9 log10基因组当量/ ml),单独3TC(2.7 log10基因组当量/ ml) )和单独的FTC(2.0 log10基因组当量/毫升)。所有治疗组中的个别土拨鼠也表现出血清WHV表面抗原的显着下降,典型地伴随着肝WHV复制和WHV抗原肝表达的下降。撤药后,大多数土拨鼠的WHV复制迅速复发,但是治疗组中的个别土拨鼠具有持续的作用。对于所施用的任何药物或药物组合,均未观察到毒性迹象。总之,在土拨鼠HBV感染模型中,单独或联合口服3TC,FTC,ADV和TDF是安全有效的。

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