Immune reconstitution in children after haploidentical haematopoietic stem cell transplantation

IF 2.2 4区 医学 Q3 HEMATOLOGY
Saranthorn Apasuthirat, Nopporn Apiwattanakul, Usanarat Anurathapan, Nintita Sripaiboonkij Thokanit, Karan Paisooksantivatana, Ekawat Pasomsub, Suradej Hongeng, Samart Pakakasama
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Abstract

Introduction

Immune reconstitution (IR) kinetics of paediatric patients underwent haploidentical haematopoietic stem cell transplantation (HSCT) with post-transplant cyclophosphamide (PTCy) have not been extensively studied. We compared IR patterns of children receiving HSCT from haploidentical (n = 92) and HLA-matched donors (n = 36), and analysed risk factors for viral infection in these patients.

Methods

We prospectively measured lymphocyte subset numbers before HSCT and at 1, 3, 6 and 12 months after HSCT. Blood cytomegalovirus (CMV), Epstein–Barr virus, adenovirus, BK virus (BKV) and urine adenovirus and BKV viral loads were measured at designated time points.

Results

The median numbers of total T and T helper cells at 1 month were significantly lower in the haploidentical group compared with the HLA-matched group. Haploidentical HSCT recipients had significantly lower median numbers of several T cell subsets and B cells for 1 year after HSCT. The median NK cell count of the haploidentical group was lower at 1 month. BKV haemorrhagic cystitis, blood CMV and urine adenovirus reactivation were more frequently found in the haploidentical group. Post-haploidentical HSCT patients receiving anti-T lymphocyte globulin (ATG) had significantly lower median numbers of total T cells (at 1 month) and T helper cells (at 6 and 12 months) and higher rate of blood BKV reactivation compared with those without ATG.

Conclusion

Paediatric patients who undergo haploidentical HSCT with PTCy are likely to have delayed IR and an increased risk of viral reactivation/infection compared with HLA-matched HSCT. The addition of ATG to PTCy delayed T cell recovery and increased risk of BKV reactivation.

Abstract Image

单倍体造血干细胞移植后儿童的免疫重建。
简介对接受单倍体造血干细胞移植(HSCT)并在移植后使用环磷酰胺(PTCy)的儿童患者的免疫重建(IR)动力学尚未进行广泛研究。我们比较了接受单倍体(92人)和HLA匹配供者(36人)造血干细胞移植的儿童的IR模式,并分析了这些患者病毒感染的风险因素。在指定的时间点测量血液中巨细胞病毒(CMV)、爱泼斯坦-巴氏病毒(Epstein-Barr virus)、腺病毒、BK病毒(BKV)以及尿液中腺病毒和BKV病毒载量。结果:与HLA配型组相比,单倍体组在1个月时总T细胞和T辅助细胞的中位数明显较低。造血干细胞移植后一年,单倍体造血干细胞移植受者的多个T细胞亚群和B细胞的中位数明显降低。单倍体组的 NK 细胞数量中位数在 1 个月时较低。在单倍体组中,BKV出血性膀胱炎、血液中CMV和尿液中腺病毒再活化的发生率更高。接受抗 T 淋巴细胞球蛋白(ATG)的单倍体造血干细胞移植后患者与未接受 ATG 的患者相比,总 T 细胞(1 个月时)和 T 辅助细胞(6 个月和 12 个月时)的中位数明显较低,血液中 BKV 再激活率较高。在 PTCy 中加入 ATG 会延迟 T 细胞的恢复,增加 BKV 再激活的风险。
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来源期刊
CiteScore
4.50
自引率
6.70%
发文量
211
审稿时长
6-12 weeks
期刊介绍: The International Journal of Laboratory Hematology provides a forum for the communication of new developments, research topics and the practice of laboratory haematology. The journal publishes invited reviews, full length original articles, and correspondence. The International Journal of Laboratory Hematology is the official journal of the International Society for Laboratory Hematology, which addresses the following sub-disciplines: cellular analysis, flow cytometry, haemostasis and thrombosis, molecular diagnostics, haematology informatics, haemoglobinopathies, point of care testing, standards and guidelines. The journal was launched in 2006 as the successor to Clinical and Laboratory Hematology, which was first published in 1979. An active and positive editorial policy ensures that work of a high scientific standard is reported, in order to bridge the gap between practical and academic aspects of laboratory haematology.
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