Division of Infectious Diseases, Duke University School of Medicine, Durham, North Carolina.
Division of Infectious Diseases, Duke University School of Medicine, Durham, North Carolina.
Am J Kidney Dis. 2023 Sep;82(3):368-372. doi: 10.1053/j.ajkd.2022.12.006. Epub 2023 Feb 4.
The transplantation of organs from donors with hepatitis C virus (HCV) infection into uninfected recipients has expanded the available organ donor pool. With the advancement of direct-acting antivirals (DAAs), high rates of cure among transplant recipients are possible. Although DAAs are highly effective, treatment failure can occur following an appropriate 12-week course of a pan-genotypic regimen. Here we describe 4 kidney transplant recipients of organs from donors with HCV infection (3 with genotype 3, 1 genotype 1a) in whom first-line DAA treatment with either glecaprevir-pibrentasvir or sofosbuvir-velpatasvir was unsuccessful, started 22-35 days after the day of transplantation. All ultimately achieved sustained virologic response with second- or third-line therapy. Post-treatment resistance-associated substitutions were tested and noted to be present in 2 cases. Additionally, antiviral levels were assessed in 2 cases and found to be therapeutic in each. This article explores possible reasons for treatment failure, including medication interactions, bariatric surgery, viral dynamics, and drug resistance.
器官移植供者丙型肝炎病毒 (HCV) 感染患者到未感染的受者,扩大了可利用的器官供者库。随着直接作用抗病毒药物 (DAA) 的进步,移植受者获得高治愈率成为可能。虽然 DAA 非常有效,但在适当的 12 周泛基因型方案疗程后,仍可能发生治疗失败。在这里,我们描述了 4 例接受 HCV 感染供者器官的肾移植受者(3 例基因型 3,1 例基因型 1a),他们在移植后第 22-35 天开始使用 glecaprevir-pibrentasvir 或 sofosbuvir-velpatasvir 进行一线 DAA 治疗,但未成功。所有患者最终通过二线或三线治疗实现持续病毒学应答。检测并记录了治疗后耐药相关替代物在 2 例中存在。此外,在 2 例中评估了抗病毒药物水平,发现每种药物的水平均具有治疗作用。本文探讨了治疗失败的可能原因,包括药物相互作用、减重手术、病毒动力学和耐药性。