直接作用抗病毒时代,同时感染基因2型丙型肝炎和来自基因1型丙型肝炎供者的HIV的受体肾移植成功

Case Reports in Hepatology Pub Date : 2020-01-29 eCollection Date: 2020-01-01 DOI:10.1155/2020/7679147
Dimitrios Farmakiotis, Zoe Weiss, Amy L Brotherton, Paul Morrissey, Reginald Gohh, Kendra Vieira, Lynn E Taylor, Joseph M Garland
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引用次数: 2

摘要

尽管在HIV感染者的移植方面取得了重大进展,但对于除基因型1以外的其他基因型丙型肝炎病毒(HCV)合并感染HIV的患者,特别是当接受不同基因型的HCV感染器官时,我们知之甚少。我们描述的第一例肾移植在一名男子合并感染丙型肝炎和艾滋病毒在我们的国家。据我们所知,这也是首例非1 (2a) HCV基因型的HIV/HCV/HBV三感染患者接受了不一致基因型(1a)的HCV感染肾移植,并在移植后转化为HCV的报道。我们的案例研究强调了以下几点:(1)移植中心需要监测HCV感染器官的等待时间,并定期评估HCV感染的移植候选人在预期从HCV感染的供体移植时延迟HCV抗病毒治疗的风险;(2)可能需要在抗hcv蛋白酶抑制剂引入和停药的早期阶段密切监测他克莫司的水平;(3)可发生供体基因型传播;(4) HIV/HCV合并感染的移植候选人需要一个整体的方法,强调心血管风险概况和心导管插入术的低阈值作为其移植前评估的一部分。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Successful Kidney Transplantation in a Recipient Coinfected with Hepatitis C Genotype 2 and HIV from a Donor Infected with Hepatitis C Genotype 1 in the Direct-Acting Antiviral Era.

Successful Kidney Transplantation in a Recipient Coinfected with Hepatitis C Genotype 2 and HIV from a Donor Infected with Hepatitis C Genotype 1 in the Direct-Acting Antiviral Era.

Successful Kidney Transplantation in a Recipient Coinfected with Hepatitis C Genotype 2 and HIV from a Donor Infected with Hepatitis C Genotype 1 in the Direct-Acting Antiviral Era.

Successful Kidney Transplantation in a Recipient Coinfected with Hepatitis C Genotype 2 and HIV from a Donor Infected with Hepatitis C Genotype 1 in the Direct-Acting Antiviral Era.

Despite significant advances in transplantation of HIV-infected individuals, little is known about HIV coinfected patients with hepatitis C virus (HCV) genotypes other than genotype 1, especially when receiving HCV-infected organs with a different genotype. We describe the first case of kidney transplantation in a man coinfected with hepatitis C and HIV in our state. To our knowledge, this is also the first report of an HIV/HCV/HBV tri-infected patient with non-1 (2a) HCV genotype who received an HCV-infected kidney graft with the discordant genotype (1a), to which he converted after transplant. Our case study highlights the following: (1) transplant centers need to monitor wait times for an HCV-infected organ and regularly assess the risk of delaying HCV antiviral treatment for HCV-infected transplant candidates in anticipation of the transplant from an HCV-infected donor; (2) closer monitoring of tacrolimus levels during the early phases of anti-HCV protease inhibitor introduction and discontinuation may be indicated; (3) donor genotype transmission can occur; (4) HIV/HCV coinfected transplant candidates require a holistic approach with emphasis on the cardiovascular risk profile and low threshold for cardiac catheterization as part of their pretransplant evaluation.

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