Management of BK Polyomavirus in a Kidney Transplant Recipient With Primary Myelofibrosis on JAK-2 Inhibition - A Case Report and Literature Review.

IF 1.6 Q3 UROLOGY & NEPHROLOGY
Canadian Journal of Kidney Health and Disease Pub Date : 2026-07-31 eCollection Date: 2026-01-01 DOI:10.1177/20543581261473484
Laura Bywater, Justin Gill, David Nicholl
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Abstract

The use of Janus Kinase (JAK) inhibitors with concomitant maintenance immunosuppressive therapy (IST) for the solid organ transplant (SOT) population presents significant challenges due to intensified immunosuppression resulting in an increased risk of opportunistic infections and malignancies coupled with limited clinical experience among transplant providers. A 48-year-old man presented with end-stage kidney disease secondary to IgA nephropathy requiring commencement of haemodialysis. He had a concurrent diagnosis of primary myelofibrosis (PMF), which did not require treatment at presentation. A year later, he underwent a living-donor kidney transplant from an HLA-identical sibling. The patient received induction IST with basiliximab and methylprednisolone, followed by standard maintenance therapy with tacrolimus and mycophenolate mofetil. The latter was reduced in dose due to underlying PMF. In the months following transplantation, he experienced worsening PMF parameters and was commenced on the JAK2 inhibitor, ruxolitinib. This was complicated by development of detectable BK Polyomavirus DNA (BKPyV-DNAemia), prompting adjustment of his immunosuppression regimen and dose reduction of ruloxlitinib. His course was further complicated by renal allograft rejection. Ruxolitinib was subsequently discontinued, and he transitioned to the second-generation JAK inhibitor fedratinib, which led to improvement in PMF parameters and stabilization of both graft function and BKPyV-DNAemia. This case highlights the therapeutic challenges inherent in integrating JAK inhibitors into established immunosuppression regimens in solid organ transplantation. It underscores the difficult balance between preserving graft tolerance and mitigating the risk of opportunistic infections such as BKPyV-DNAemia, while emphasising the need for close monitoring of net immunosuppression in this setting.

JAK-2抑制对原发性骨髓纤维化肾移植受者BK多瘤病毒的治疗——一例报告和文献综述
由于强化的免疫抑制导致机会性感染和恶性肿瘤的风险增加,加上移植提供者的临床经验有限,在实体器官移植(SOT)人群中使用Janus激酶(JAK)抑制剂联合维持免疫抑制治疗(IST)面临重大挑战。一个48岁的男性提出终末期肾脏疾病继发IgA肾病需要开始血液透析。他同时被诊断为原发性骨髓纤维化(PMF),在就诊时不需要治疗。一年后,他接受了来自hla完全相同的兄弟姐妹的活体肾脏移植手术。患者接受basiliximab和methylprednisolone诱导IST,随后使用他克莫司和霉酚酸酯进行标准维持治疗。后者的剂量由于潜在的PMF而减少。在移植后的几个月里,他经历了PMF参数的恶化,并开始使用JAK2抑制剂ruxolitinib。可检测到的BK多瘤病毒DNA (BKPyV-DNAemia)的发展使其复杂化,促使他调整免疫抑制方案并减少ruloxlitinib的剂量。他的病程因肾移植排斥反应而进一步复杂化。随后,Ruxolitinib被停用,他转而使用第二代JAK抑制剂fedratinib,这导致PMF参数改善,移植物功能和BKPyV-DNAemia稳定。该病例强调了在实体器官移植中将JAK抑制剂整合到已建立的免疫抑制方案中所固有的治疗挑战。它强调了在保持移植物耐受性和减轻机会性感染(如BKPyV-DNAemia)风险之间的困难平衡,同时强调了在这种情况下密切监测净免疫抑制的必要性。
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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来源期刊
CiteScore
3.00
自引率
5.90%
发文量
84
审稿时长
12 weeks
期刊介绍: Canadian Journal of Kidney Health and Disease, the official journal of the Canadian Society of Nephrology, is an open access, peer-reviewed online journal that encourages high quality submissions focused on clinical, translational and health services delivery research in the field of chronic kidney disease, dialysis, kidney transplantation and organ donation. Our mandate is to promote and advocate for kidney health as it impacts national and international communities. Basic science, translational studies and clinical studies will be peer reviewed and processed by an Editorial Board comprised of geographically diverse Canadian and international nephrologists, internists and allied health professionals; this Editorial Board is mandated to ensure highest quality publications.
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