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Mutations in hepatitis C virus NS3 protease domain associated with resistance to specific protease inhibitors in antiviral therapy naive patients.

机译:丙型肝炎病毒NS3蛋白酶结构域中的突变与未接受过抗病毒治疗的患者对特定蛋白酶抑制剂的抗性相关。

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摘要

The prevalence of naturally occurring mutations in hepatitis C virus associated with resistance to protease inhibitors in chronically infected patients has not been reported in Brazil. The NS3 serine protease domain was sequenced in 114 therapy-naive patients infected with subtype 1a (n = 48), 1b (n = 53), or 3a (n = 13). A V36L mutation was observed in 5.6% patients infected with subtype 1b and in all isolates of the 3a subtype, and a T54S mutation was detected in 4.1% of isolates of subtype 1a. In conclusion, the presence of variants carrying mutations associated with resistance to protease inhibitors in therapy-naive patients may be important for future therapeutic strategies.
机译:在巴西,尚未报道丙型肝炎病毒中自然发生的突变与慢性感染患者对蛋白酶抑制剂的抵抗有关。在114名未接受治疗的亚型1a(n = 48),1b(n = 53)或3a(n = 13)感染的患者中对NS3丝氨酸蛋白酶结构域进行了测序。在5.6%的1b亚型感染者和3a亚型的所有分离株中均观察到V36L突变,在4.1%的1a亚型的分离株中检测到T54S突变。总之,在未经治疗的患者中,存在携带与蛋白酶抑制剂耐药相关的突变的变体可能对未来的治疗策略很重要。

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