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Development of tenofovir disoproxil fumarate resistance after complete viral suppression in a patient with treatment-na?ve chronic hepatitis B: A case report and review of the literature

机译:初治慢性乙型肝炎患者完全抑制病毒后对替诺福韦酯富马酸富马酸耐药的发生:一例病例并文献复习

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Tenofovir disoproxil fumarate (TDF) is a potent nucleotide analogue that is recommended as first-line therapy for patients with chronic hepatitis B. The results of a longitudinal study of TDF treatment demonstrated no development of resistance. We observed one treatment-na?ve chronic hepatitis B (CHB) patient who developed TDF resistance after complete viral suppression during long-term TDF treatment. A 37-year-old HBeAg-positive man received TDF 300 mg/d for 43 mo. The hepatitis B virus (HBV) DNA titer was 8 log10 copies/mL at baseline and became undetectable at 16 mo after treatment. However, the HBV DNA titer rebounded to 7.5 log10 copies/mL at 43 mo after treatment. We performed full sequencing to find mutation sites associated with virologic breakthrough. The results showed 9 mutation sites, most of which had not been well-known as mutation sites. We changed the therapy from tenofovir to entecavir with a regimen of 0.5 mg once daily. After 4 mo, the HBV DNA titer decreased to 267 copies/mL, and the liver enzyme levels were normalized.
机译:替诺福韦富马酸替索罗非酯(TDF)是一种有效的核苷酸类似物,推荐作为慢性乙型肝炎患者的一线治疗。TDF治疗的纵向研究结果表明未产生耐药性。我们观察到一名初治的慢性乙型肝炎(CHB)患者在长期TDF治疗期间完全抑制病毒后出现TDF耐药性。一名37岁的HBeAg阳性男子接受TDF 300 mg / d治疗,持续43个月。基线时,乙型肝炎病毒(HBV)DNA滴度为8 log 10 拷贝/ mL,治疗后16个月未检测到。然而,治疗后43个月,HBV DNA滴度回升至7.5 log 10 拷贝/ mL。我们进行了完整的测序,以发现与病毒学突破相关的突变位点。结果显示有9个突变位点,其中大多数都不是众所周知的突变位点。我们将疗法从替诺福韦改为恩替卡韦,每天一次0.5 mg。 4个月后,HBV DNA滴度降至267拷贝/ mL,肝酶水平恢复正常。

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