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异体造血细胞移植使用阿仑单抗治疗亚洲免疫性先天缺陷患者。

Allogeneic Hematopoietic cell Transplantation Using Alemtuzumab in Asian Patients with Inborn Errors of Immunity.

机构信息

Department of Pediatrics and Developmental Biology, Tokyo Medical and Dental University (TMDU), Tokyo, Japan.

Department of Child Health and Development, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University (TMDU), 1-5-45 Yushima, Bunkyo-ku, Tokyo, 113-8519, Japan.

出版信息

J Clin Immunol. 2024 May 22;44(6):126. doi: 10.1007/s10875-024-01734-5.

DOI:10.1007/s10875-024-01734-5
PMID:38773000
Abstract

Alemtuzumab is used with reduced-toxicity conditioning (RTC) in allogeneic hematopoietic cell transplantation (HCT), demonstrating efficacy and feasibility for patients with inborn errors of immunity (IEI) in Western countries; however, the clinical experience in Asian patients with IEI is limited. We retrospectively analyzed patients with IEI who underwent the first allogeneic HCT with alemtuzumab combined with RTC regimens in Japan. A total of 19 patients were included and followed up for a median of 18 months. The donors were haploidentical parents (n = 10), matched siblings (n = 2), and unrelated bone marrow donors (n = 7). Most patients received RTC regimens containing fludarabine and busulfan and were treated with 0.8 mg/kg alemtuzumab with intermediate timing. Eighteen patients survived and achieved stable engraftment, and no grade 3-4 acute graft-versus-host disease was observed. Viral infections were observed in 11 patients (58%) and 6 of them presented symptomatic. The median CD4 T cell count was low at 6 months (241/µL) but improved at 1 year (577/µL) after HCT. Whole blood cells continued to exhibit > 80% donor type in most cases; however, 3/10 patients exhibited poor donor chimerism only among T cells and also showed undetectable levels of T-cell receptor recombination excision circles (TRECs) at 1 year post-HCT. This study demonstrated the efficacy and safety of alemtuzumab; however, patients frequently developed viral infections and slow reconstitution or low donor chimerism in T cells, emphasizing the importance of monitoring viral status and T-cell-specific chimerism. (238 < 250 words).

摘要

阿仑单抗联合减毒预处理方案(RTC)在异基因造血细胞移植(HCT)中用于治疗遗传性免疫缺陷病(IEI)患者,在西方国家显示出疗效和可行性;然而,亚洲 IEI 患者的临床经验有限。我们回顾性分析了日本接受阿仑单抗联合 RTC 方案行首次异基因 HCT 的 IEI 患者。共纳入 19 例患者,中位随访时间为 18 个月。供者为单倍体父母(n = 10)、同胞全相合供者(n = 2)和无关供者(n = 7)。大多数患者接受含氟达拉滨和白消安的 RTC 方案,并于中等时间点给予 0.8 mg/kg 阿仑单抗。18 例患者存活并获得稳定的植入,未观察到 3-4 级急性移植物抗宿主病。11 例患者(58%)发生病毒感染,其中 6 例出现症状。HCT 后 6 个月 CD4 T 细胞计数中位数较低(241/µL),1 年后(577/µL)改善。大多数情况下,全血细胞仍表现出 > 80%的供者类型;然而,3/10 例患者仅在 T 细胞中表现出较差的供者嵌合,并且在 HCT 后 1 年时 T 细胞受体重组切除环(TREC)也检测不到。本研究显示了阿仑单抗的疗效和安全性;然而,患者经常发生病毒感染,T 细胞重建缓慢或嵌合度低,强调监测病毒状态和 T 细胞特异性嵌合的重要性。(238 < 250 字)。

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本文引用的文献

1
Alemtuzumab-based reduced-intensity conditioning for XIAP deficiency.基于阿仑单抗的减低强度预处理用于X连锁凋亡抑制蛋白缺乏症。
Pediatr Int. 2023 Jan-Dec;65(1):e15576. doi: 10.1111/ped.15576.
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Exposure-response analysis of alemtuzumab in pediatric allogeneic HSCT for nonmalignant diseases: the ARTIC study.阿仑单抗治疗儿科非恶性疾病异基因造血干细胞移植的暴露-反应分析:ARTIC 研究。
Blood Adv. 2023 Aug 22;7(16):4462-4474. doi: 10.1182/bloodadvances.2022009051.
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Wiskott-Aldrich syndrome with normal-sized platelets.血小板大小正常的维斯科特-奥尔德里奇综合征
Pediatr Int. 2023 Jan;65(1):e15453. doi: 10.1111/ped.15453.
4
Case report: HLA-haploidentical hematopoietic cell transplant with posttransplant cyclophosphamide in a patient with leukocyte adhesion deficiency type I.病例报告:白细胞黏附缺陷症 I 型患者接受 HLA 单倍体相合造血细胞移植和移植后环磷酰胺治疗。
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B-Cell Immune Reconstitution with Mixed Chimerism After Hematopoietic Cell Transplantation in a Patient with Severe Combined Immunodeficiency.严重联合免疫缺陷患者造血细胞移植后混合嵌合体状态下的B细胞免疫重建
J Clin Immunol. 2022 Oct;42(7):1392-1395. doi: 10.1007/s10875-022-01311-8. Epub 2022 Jun 27.
6
Model-informed precision dosing for alemtuzumab in paediatric and young adult patients undergoing allogeneic haematopoietic cell transplantation.基于模型的精准剂量调整在儿科和年轻成年异体造血细胞移植患者中应用的阿仑单抗治疗。
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A risk-stratified therapy for infants with acute lymphoblastic leukemia: a report from the JPLSG MLL-10 trial.分层风险治疗急性淋巴细胞白血病患儿:来自 JPLSG MLL-10 试验的报告。
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Impact of alemtuzumab pharmacokinetics on T-cell dynamics, graft-versus-host disease and viral reactivation in patients receiving allogeneic stem cell transplantation with an alemtuzumab-based T-cell-depleted graft.来氟米特联合吗替麦考酚酯预防肾移植术后急性排斥反应的临床观察 目的:观察来氟米特(LEF)联合吗替麦考酚酯(MMF)预防肾移植术后急性排斥反应的疗效及安全性。 方法:回顾性分析 46 例接受肾移植的患者,其中 24 例术后采用LEF+MMF(LEF 组),22 例采用环孢素A(CsA)+吗替麦考酚酯(MMF)(CsA 组)。比较两组患者的急性排斥反应发生率、肾功能、药物不良反应等。 结果:两组患者在性别、年龄、原发病、移植肾来源、免疫抑制方案等方面无统计学差异。LEF 组患者在术后 1 年和 3 年的急性排斥反应发生率明显低于CsA 组(P<0.05),肾功能明显优于CsA 组(P<0.05)。两组患者在药物不良反应发生率方面无统计学差异。 结论:LEF 联合MMF 方案预防肾移植术后急性排斥反应的疗效优于CsA+MMF 方案,且安全性良好。
Transpl Immunol. 2019 Dec;57:101209. doi: 10.1016/j.trim.2019.06.001. Epub 2019 Jun 14.
9
Droplet Digital PCR-Based Chimerism Analysis for Primary Immunodeficiency Diseases.基于液滴数字 PCR 的原发性免疫缺陷病嵌合体分析。
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Multicolor Flow Cytometry for the Diagnosis of Primary Immunodeficiency Diseases.用于原发性免疫缺陷病诊断的多色流式细胞术
J Clin Immunol. 2017 Jul;37(5):486-495. doi: 10.1007/s10875-017-0405-7. Epub 2017 Jun 8.