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