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儿童心脏移植受者的单药免疫抑制治疗

Monotherapy Immunosuppression in Pediatric Heart Transplant Recipients.

作者信息

Profita Elizabeth L, Lee Joanne, Lee Donna, Barkoff Lynsey, Wujcik Kari, Chen Chiu-Yu, Bernstein Daniel, Hollander Seth A

机构信息

Department of Pediatrics (Cardiology), Stanford University, Palo Alto, California, USA.

Pediatric Solid Organ Transplant Center, Lucile Packard Children's Hospital Stanford, Palo Alto, California, USA.

出版信息

Pediatr Transplant. 2025 Sep;29(6):e70157. doi: 10.1111/petr.70157.

Abstract

BACKGROUND

Although dual-drug immunosuppression is standard for rejection prophylaxis in pediatric heart transplant (HT), single-drug immunosuppression (monotherapy) may be appropriate for certain patients. We describe the experience with monotherapy in select patients at a single institution.

METHODS

Retrospective review of HT patients at a pediatric transplant center who underwent HT between 1/2001-12/2020 and were treated with calcineurin-inhibitor monotherapy for > 1 month. Patients were transitioned to monotherapy due to concerns for over-immune suppression, including recurrent infection, neutropenia, or post-transplant lymphoproliferative disorder (PTLD). Clinical characteristics and patient outcomes were analyzed.

RESULTS

During the study period, 16/318 (5%) HT patients were placed on monotherapy at a median of 4.6 years post-HT (IQR 1.8-6.9 years). Most patients on monotherapy were transplanted as infants (81%, 13/16), 56% (9/16) were male, and 50% (8/16) underwent HT for congenital heart disease (CHD). Most (81%) were on tacrolimus monotherapy. The indication for monotherapy was recurrent infection in 50%, PTLD in 31%, and neutropenia in 19%. At a median follow-up of 1.5 years (IQR 1.1-2.2 years), there were no episodes of moderate or greater rejection and no evidence of coronary allograft vasculopathy. At last follow-up, 87% of patients remain on monotherapy, and 94% of patients are alive and well, including one patient who has continued monotherapy for over 15 years.

CONCLUSIONS

Monotherapy immunosuppression with calcineurin inhibitors may be preferred in a subset of pediatric HT patients with evidence of over-immune suppression without conferring increased risk of rejection.

摘要

背景

虽然双联免疫抑制是小儿心脏移植(HT)中预防排斥反应的标准疗法,但单药免疫抑制(单一疗法)可能适用于某些患者。我们描述了在单一机构中对选定患者采用单一疗法的经验。

方法

回顾性分析一家儿科移植中心在2001年1月至2020年12月期间接受HT且接受钙调神经磷酸酶抑制剂单一疗法治疗超过1个月的患者。由于担心免疫抑制过度,包括反复感染、中性粒细胞减少或移植后淋巴细胞增生性疾病(PTLD),患者被转换为单一疗法。分析临床特征和患者预后。

结果

在研究期间,16/318(5%)的HT患者在HT后中位4.6年(四分位间距1.8 - 6.9年)开始接受单一疗法。接受单一疗法的大多数患者为婴儿期接受移植(81%,13/16),56%(9/16)为男性,50%(8/16)因先天性心脏病(CHD)接受HT。大多数(81%)接受他克莫司单一疗法。单一疗法的指征为反复感染占50%,PTLD占31%,中性粒细胞减少占19%。中位随访1.5年(四分位间距1.1 - 2.2年)时,无中度或更严重排斥反应发作,也无冠状动脉移植血管病变的证据。在最后一次随访时,87%的患者仍在接受单一疗法,94%的患者存活且状况良好,包括一名持续接受单一疗法超过15年的患者。

结论

对于有免疫抑制过度证据且无排斥反应风险增加的部分小儿HT患者,钙调神经磷酸酶抑制剂单一疗法免疫抑制可能是更优选择。

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