造血细胞移植治疗先天性免疫缺陷儿童的疗效:单中心研究

IF 7.2 2区 医学 Q1 IMMUNOLOGY Journal of Clinical Immunology Pub Date : 2024-12-27 DOI:10.1007/s10875-024-01853-z
Hasan Hashem, Lubna Ghatasheh, Rula Najjar, Duaa Mufarrej, Duaa Zandaki, Mayada Abu Shanap, Eman Khattab, Rawad Rihani, Iyad Sultan
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引用次数: 0

摘要

先天性免疫错误(IEI)是一组异质性的罕见单基因疾病,影响先天或适应性免疫,导致对危及生命的感染和自身免疫的易感性。同种异体造血细胞移植(HCT)是治疗儿童IEI的一个有价值的选择。我们对IEI患儿HCT的结果进行了一项回顾性的单中心研究。主要终点为总生存期(OS)。我们收集了2014年至2023年期间接受HCT的55例患者的数据。HCT的适应症为CGD (n = 14)、HLH (n = 12)、SCID (n = 10)和其他(n = 19)。HCT的中位年龄为3岁(范围0.1-17岁)。供者为hla匹配的亲属(n = 27)、单倍同型(n = 24)和脐带血(n = 4)。预处理方案为清髓性(n = 34)、降低强度(n = 18)或无预处理(n = 3)。中位随访43个月(13-120个月)后,2年OS为93%,2年EFS为79%,2年无gvhd无复发生存率(GRFS)为69%。单因素分析显示,骨髓来源与较好的EFS和GRFS显著相关。2-4级急性和中/重度慢性GvHD的累积发病率分别为21%和13%。移植失败的发生率为13%。总之,HCT治疗儿童IEI是可行且有效的。早期诊断和转诊以及及时治疗可以进一步改善预后。
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Outcomes of Hematopoietic Cell Transplantation in Children with Inborn Errors of Immunity: A Single-Center Series.

Inborn errors of immunity (IEI) are a heterogenous group of rare monogenic disorders that affect innate or adaptive immunity, resulting in susceptibility to life-threatening infections and autoimmunity. Allogeneic hematopoietic cell transplantation (HCT) is a valuable curative option for children with IEI. We conducted a retrospective single-center study on the outcome of HCT in children with IEI. Primary outcome was overall survival (OS). We gathered data from 55 patients underwent HCT in the period 2014 to 2023. The indications for HCT were CGD (n = 14), HLH (n = 12), SCID (n = 10), and others (n = 19). Median age at HCT was 3 years (range 0.1-17). Donors were HLA-matched related (n = 27), haploidentical (n = 24), and cord (n = 4). The conditioning regimens were myeloablative (n = 34), reduced intensity (n = 18), or no conditioning (n = 3). After a median follow-up of 43 months (range 13-120), 2-year OS was 93%, 2-year EFS 79% and 2 year GvHD-free relapse-free survival (GRFS) was 69%. Univariate analysis showed that bone marrow source was significantly associated with better EFS and GRFS. Cumulative incidence of grade 2-4 acute and moderate/severe chronic GvHD were 21% and 13%, respectively. Incidence of graft failure was 13%. In conclusion, HCT is feasible and curative in children with IEI. Early diagnosis and referral in addition to timely treatment can further improve outcomes.

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来源期刊
CiteScore
12.20
自引率
9.90%
发文量
218
审稿时长
2 months
期刊介绍: The Journal of Clinical Immunology publishes impactful papers in the realm of human immunology, delving into the diagnosis, pathogenesis, prognosis, or treatment of human diseases. The journal places particular emphasis on primary immunodeficiencies and related diseases, encompassing inborn errors of immunity in a broad sense, their underlying genotypes, and diverse phenotypes. These phenotypes include infection, malignancy, allergy, auto-inflammation, and autoimmunity. We welcome a broad spectrum of studies in this domain, spanning genetic discovery, clinical description, immunologic assessment, diagnostic approaches, prognosis evaluation, and treatment interventions. Case reports are considered if they are genuinely original and accompanied by a concise review of the relevant medical literature, illustrating how the novel case study advances the field. The instructions to authors provide detailed guidance on the four categories of papers accepted by the journal.
期刊最新文献
ATM Expression and Activation in Ataxia Telangiectasia Patients with and without Class Switch Recombination Defects. Pre-Transplant Immune Dysregulation Predicts for Poor Outcome Following Allogeneic Haematopoietic Stem Cell Transplantation in Adolescents and Adults with Inborn Errors of Immunity (IEI). Outcomes of Hematopoietic Stem Cell Transplantation in 5 Patients with Autosomal Recessive RIPK1-Deficiency. Novel Inherited N-terminus TAP1 Variants and Severe Clinical Manifestations- Are Genotype-Phenotype Correlations Emerging? Baricitinib-Induced Remission of Alopecia Universalis in a Child with NFKB2-Associated Immune Dysregulation.
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