Pharmacokinetics of maraviroc in plasma and breastmilk in a treatment-experienced perinatally HIV-1-infected woman

C. Feiterna-Sperling, R. Krüger, A. Amara, S. Khoo, C. Waitt
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引用次数: 1

Abstract

Maraviroc (MVC), a C-C chemokine receptor type five (CCR5) antagonist, was approved as part of combination antiretroviral therapy (cART) in 2007, for use in treatment-experienced adults infected with CCR5tropic HIV-1 [1]. Whilst, with current treatment strategies, such as maternal cART, low rates of mother-to-child transmission (MTCT) have been reported, in high-income countries, breastfeeding is not recommended because of the potential MTCT risk. However, since 2017, European [2] and United States [3] guidelines have acknowledged that some HIV-infected women may wish to breastfeed, and should be given appropriate support in this decision. Whilst data exist describing the transfer of NRTI, NNRTI, and protease inhibitors to breastfed infants [4,5], the pharmacokinetics and safety of MVC in lactating women and their breastfed infants have not been reported. Here, we present the first case of MVC in a breastfeeding mother.
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马拉维洛克在围产期hiv -1感染妇女血浆和母乳中的药代动力学
Maraviroc (MVC)是一种C-C趋化因子受体5型(CCR5)拮抗剂,于2007年被批准作为联合抗逆转录病毒治疗(cART)的一部分,用于治疗经验丰富的成人感染CCR5型HIV-1[1]。虽然目前的治疗策略,如孕产妇cART,报告了较低的母婴传播率,但在高收入国家,由于潜在的母婴传播风险,不建议母乳喂养。然而,自2017年以来,欧洲[3]和美国[3]指南承认,一些感染艾滋病毒的妇女可能希望母乳喂养,应在这一决定中给予适当支持。虽然已有数据描述NRTI、NNRTI和蛋白酶抑制剂向母乳喂养的婴儿转移[4,5],但MVC在哺乳期妇女及其母乳喂养的婴儿中的药代动力学和安全性尚未报道。在这里,我们提出了第一例母乳喂养母亲的MVC。
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