减少剂量西多福韦和巨细胞病毒高免疫球蛋白治疗轻度更昔洛韦耐药巨细胞病毒病

IF 0.9 Q3 SURGERY Journal of Transplantation Pub Date : 2014-01-01 Epub Date: 2014-06-01 DOI:10.1155/2014/342319
Samir J Patel, Samantha A Kuten, Richard J Knight, Dana M Hong, A Osama Gaber
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引用次数: 11

摘要

更昔洛韦耐药巨细胞病毒(CMV)与实体器官移植受者的显著发病率相关。更昔洛韦耐药巨细胞病毒的治疗可能会因肾毒性而复杂化,肾毒性通常在推荐的治疗和/或“间接”病毒作用或减少免疫抑制引起的排斥反应中观察到。在此,我们报告了4例诊断为更昔洛韦耐药CMV疾病的高血清学风险(供体CMV阳性/受体CMV阴性)肾移植患者。所有患者在移植后仍接受缬更昔洛韦预防治疗时,最初都出现了“突破性”病毒血症,后来在服用足够剂量的缬更昔洛韦未能根除病毒后,证实出现了UL97突变。随后,患者成功地接受了减少剂量(1- 2mg /kg)西多福韦和巨细胞病毒高免疫球蛋白的治疗,每隔2周给予一次。此外,所有患者在完成治疗后均表现出稳定的肾功能,未发生急性排斥反应。减少剂量西多福韦和巨细胞病毒高免疫球蛋白联合治疗对更昔洛韦耐药巨细胞病毒引起的轻度疾病是一种安全有效的治疗方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Resolution of Mild Ganciclovir-Resistant Cytomegalovirus Disease with Reduced-Dose Cidofovir and CMV-Hyperimmune Globulin.

Ganciclovir-resistant cytomegalovirus (CMV) is associated with significant morbidity in solid organ transplant recipients. Management of ganciclovir-resistant CMV may be complicated by nephrotoxicity which is commonly observed with recommended therapies and/or rejection induced by "indirect" viral effects or reduction of immunosuppression. Herein, we report a series of four high serologic risk (donor CMV positive/recipient CMV negative) kidney transplant patients diagnosed with ganciclovir-resistant CMV disease. All patients initially developed "breakthrough" viremia while still receiving valganciclovir prophylaxis after transplant and were later confirmed to exhibit UL97 mutations after failing to eradicate virus on adequate dosages of valganciclovir. The patients were subsequently and successfully treated with reduced-dose (1-2 mg/kg) cidofovir and CMV-hyperimmune globulin, given in 2-week intervals. In addition, all patients exhibited stable renal function after completion of therapy, and none experienced acute rejection. The combination of reduced-dose cidofovir and CMV-hyperimmune globulin appeared to be a safe and effective regimen in patients with mild disease due to ganciclovir-resistant CMV.

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自引率
4.00%
发文量
5
审稿时长
16 weeks
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