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Greater suppression of nevirapine resistance with 21- vs 7-day antiretroviral regimens after intrapartum single-dose nevirapine for prevention of mother-to-child transmission of HIV

机译:产后单剂量奈韦拉平治疗后21天和7天抗逆转录病毒疗法可更大程度地抑制奈韦拉平耐药,以预防HIV母婴传播

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Background. Nevirapine (NVP) resistance emerges in up to 70% of women exposed to single-dose (sd) NVP for prevention of mother-to-child transmission of human immunodeficiency virus (HIV). Methods. HIV-infected pregnant women were randomized to receive sdNVP and either zidovudine/lamivudine (3TC), tenofovir/emtricitabine (FTC), or lopinavir/ritonavir for either 7 or 21 days. The primary endpoint was the emergence of new NVP resistance mutations as detected by standard population genotype at 2 and 6 weeks after treatment. Low-frequency NVP- or 3TC/FTC-resistant mutants at codons 103, 181, and 184 were sought using allele-specific polymerase chain reaction (ASP). Results. Among 484 women randomized, 422 (87%) received study treatment. Four hundred twelve (98%) women had primary endpoint results available; of these, 5 (1.2%) had new NVP resistance detected by population genotype: 4 of 215 in the 7-day arms (1.9%; K103N in 4 women with Y181C, Y188C, or G190A in 3 of 4) and 1 of 197 (0.5%; V108I) in the 21-day arms (P = .37). Among women with ASP results, new NVP resistance mutations emerged significantly more often in the 7-day arms (13/74 [18%]) than in the 21-day arms (3/66 [5%], P = .019). 3TC/ FTC-resistant mutants (M184V/I) emerged infrequently (7/134 [5%]), and their occurrence did not differ by arm. Conclusions. Three short-term antiretroviral strategies, begun simultaneously with the administration of sdNVP, resulted in a low rate (1.2%) of new NVP-resistance mutations when assessed at 2 and 6 weeks following completion of study treatment by standard genotype. ASP revealed that 21-day regimens were significantly better than 7-day regimens at preventing the emergence of minor NVP resistance variants. ? The Author 2012. Published by Oxford University Press on behalf of the Infectious Diseases Society of America.
机译:背景。奈韦拉平(NVP)耐药性的最高暴露于单剂量(sd)NVP的妇女中,以预防人类免疫缺陷病毒(HIV)的母婴传播。方法。被HIV感染的孕妇随机接受sdNVP和齐多夫定/拉米夫定(3TC),替诺福韦/恩曲他滨(FTC)或洛匹那韦/利托那韦7天或21天。主要终点是治疗后第2周和第6周通过标准人群基因型检测到的新的NVP抗性突变的出现。使用等位基因特异性聚合酶链反应(ASP)寻找位于103、181和184位密码子的耐NVP或3TC / FTC的低频突变体。结果。在随机分配的484名妇女中,有422名(87%)接受了研究治疗。 412名(98%)妇女有主要终点结果可用;其中有5(1.2%)个具有新的NVP耐药性,分别是:7天组中有215个中有4个(1.9%; 4个中有Y181C,Y188C或G190A的4名妇女中K103N)和197个中的1个(0.5%; V108I)在21天治疗组中(P = 0.37)。在有ASP结果的女性中,新的NVP抵抗突变在7天治疗组(13/74 [18%])的出现频率明显高于21天治疗组(3/66 [5%],P = .019) 。很少出现3TC / FTC抗性突变体(M184V / I)(7/134 [5%]),并且它们的出现在臂上没有差异。结论在通过标准基因型完成研究治疗后第2周和第6周评估时,与sdNVP给药同时开始的三种短期抗逆转录病毒策略导致新的NVP耐药突变率较低(1.2%)。 ASP显示21天治疗方案在预防次要NVP耐药性变异方面显着优于7天治疗方案。 ?作者2012。由牛津大学出版社代表美国传染病学会出版。

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