Bodyweight and Absolute Lymphocyte Count-Based Dosing of Rabbit Anti-thymocyte Globulin Results in Early CD4+ Immune Reconstitution in Patients with Inborn Errors of Metabolism Undergoing Umbilical Cord Blood Transplantation

IF 3.6 3区 医学 Q2 HEMATOLOGY
Daniel Drozdov , Jessica Kandil , Susie E. Long , Connor V. Demorest , Qing Cao , Troy C. Lund , Ashish O. Gupta , Jaap Jan Boelens , Paul J. Orchard
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Abstract

Background

Rabbit anti-thymocyte globulin (rATG) decreases the risk of graft failure and graft-versus-host disease (GVHD) in a setting of allogenic hematopoietic cell transplantation (HCT) but has highly variable pharmacokinetics. Recently, it was shown that a dosing nomogram based on recipient bodyweight and absolute lymphocyte count reduced rATG overexposure, which led to faster immune reconstitution. The aim of this study is to evaluate the feasibility and benefits of using an rATG dosing nomogram to achieve early CD4+ immune reconstitution in pediatric patients with inborn errors of metabolism (IEM) undergoing umbilical cord blood transplantation.

Methods

The rATG dosing nomogram in pediatric patients with IEM receiving an umbilical cord blood transplant with busulfan-based myeloablative conditioning at the University of Minnesota Masonic Children's Hospital was used prospectively since 2017. The primary endpoint was CD4+ immune reconstitution (>50 CD4+ T-cells/mL) within 100 days after HCT. Secondary endpoints included overall survival, graft failure, acute and chronic GVHD, and viral reactivations.

Results

A total of 27 patients were included in the study. Median follow-up time was 31 months (interquartile range [IQR], 22-38) and median age was 1.5 years (IQR, 0.7-3.9). The underlying disease was Hurler syndrome in 17 (63%), Hunter syndrome in 4 (15%), and cerebral adrenoleukodystrophy in 4 (15%) patients; 2 patients were transplanted for other IEM. The CD4+ recovery (>50 CD4+ T cells/mL) at 100 days post-HCT was reached in 22 (85%) of 26 patients. Overall survival was 83% (95% confidence interval [CI], 67%-100%). No graft failure was observed. Two (7%) patients developed acute GVHD grade II to IV and no patients had chronic GVHD. Six patients (22%) had cytomegalovirus (CMV) viremia. One patient had Epstein-Barr virus reactivation requiring treatment.

Conclusion

In patients with IEM, individualized dosing of rATG was associated with a robust and early CD4+ immune reconstitution, with no graft failures and low GVHD incidence.
以体重和绝对淋巴细胞计数为基础给药兔抗胸腺细胞球蛋白对先天性代谢异常脐血移植患者早期CD4+免疫重建的影响
背景:兔抗胸腺细胞球蛋白(rATG)降低同种异体造血细胞移植(HCT)中移植物失败和移植物抗宿主病(GvHD)的风险,但具有高度可变的药代动力学。最近,研究表明,基于受体体重和绝对淋巴细胞计数的给药图可减少大鼠g过度暴露,从而加快免疫重建。本研究的目的是评估在接受脐带血移植的先天性代谢错误(IEM)儿童患者中使用rATG给药图实现早期CD4+免疫重建的可行性和益处。方法:自2017年以来,在明尼苏达大学共济会儿童医院接受脐带血移植的IEM儿童患者的rATG剂量图进行前瞻性研究。主要终点是HCT后100天内CD4+免疫重建(50 CD4+ t细胞/mL)。次要终点包括总生存期、移植物衰竭、急性和慢性GvHD以及病毒再激活。结果:27例患者纳入研究。中位随访时间为31个月(IQR 22 ~ 38),中位年龄为1.5岁(IQR 0.7 ~ 3.9)。基础疾病为Hurler综合征17例(63%),Hunter综合征4例(15%),脑肾上腺白质营养不良4例(15%),2例移植其他IEM。26例患者中有22例(85%)在HCT后100天达到CD4+恢复(50 CD4+ t细胞/mL)。总生存率为83% (95% CI 67% ~ 100%)。未见移植物衰竭。2例(7%)患者发展为急性GvHD II至IV级,没有患者发展为慢性GvHD。6例(22%)有巨细胞病毒血症。一名患者患有eb病毒再激活,需要治疗。结论:在IEM患者中,个体化剂量的rATG与强大的早期CD4+免疫重建相关,无移植物衰竭和低GvHD发生率。
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
7.00
自引率
15.60%
发文量
1061
审稿时长
51 days
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