Sato Tomonobu, Kobayashi Ryoji, Toita Nariaki, Kaneda Makoto, Hatano Norikazu, Iguchi Akihiro, Kawamura Nobuaki, Ariga Tadashi
Department of Pediatrics, Hokkaido University Graduate School of Medicine, Sapporo, Japan.
Pediatr Int. 2007 Dec;49(6):795-800. doi: 10.1111/j.1442-200X.2007.02468.x.
Primary immunodeficiency diseases (PID) are rare but have a high associated risk of death from overwhelming infection in early childhood. Stem cell transplantation (SCT) can be curative for PID, but standardized protocols for each disease have not yet been established.
Between May 1995 and May 2005, nine patients diagnosed with a PID received SCT at the Department of Pediatrics, Hokkaido University Hospital. The median age of the patients (eight boys and one girl) was 1.0 year (range: 6 months-4 years). Five patients had Wiskott-Aldrich syndrome (WAS), three had severe combined immunodeficiency (SCID), and one had X-linked hyper-IgM syndrome (X-HIGM). Four patients received bone marrow transplantation (BMT), and five received cord blood stem cell transplantation (CBSCT). All patients, including those with SCID, received a conditioning regimen: six (WAS and X-HIGM) received a myeloablative conditioning regimen, and three (SCID) received a reduced-intensity conditioning regimen.
All the patients are alive and have stable, complete chimerism, based on a median follow-up period of 4 years. Moreover, all patients have good immune reconstitution, and none required immunoglobulin replacement therapy. Two patients had significant acute graft-versus-host disease (GVHD), and three patients had chronic GVHD. Four of the nine patients developed cytomegalovirus (CMV) infection after SCT.
The transplantation procedures appear to have provided a permanent cure in nine PID patients. Early diagnosis and prompt performance of SCT with an optimal donor and conditioning regimen contributed to the favorable outcomes.
原发性免疫缺陷病(PID)较为罕见,但在儿童早期因严重感染导致死亡的风险较高。干细胞移植(SCT)可治愈PID,但尚未建立针对每种疾病的标准化方案。
1995年5月至2005年5月期间,9例被诊断为PID的患者在北海道大学医院儿科接受了SCT。患者(8名男孩和1名女孩)的中位年龄为1.0岁(范围:6个月至4岁)。5例患有Wiskott-Aldrich综合征(WAS),3例患有严重联合免疫缺陷病(SCID),1例患有X连锁高IgM综合征(X-HIGM)。4例患者接受了骨髓移植(BMT),5例接受了脐血干细胞移植(CBSCT)。所有患者,包括SCID患者,均接受了预处理方案:6例(WAS和X-HIGM)接受了清髓性预处理方案,3例(SCID)接受了减低强度预处理方案。
基于4年的中位随访期,所有患者均存活且具有稳定、完全的嵌合体。此外,所有患者的免疫重建良好,均无需免疫球蛋白替代治疗。2例患者发生了严重的急性移植物抗宿主病(GVHD),3例患者发生了慢性GVHD。9例患者中有4例在SCT后发生了巨细胞病毒(CMV)感染。
移植程序似乎为9例PID患者提供了永久性治愈。早期诊断并及时采用最佳供体和预处理方案进行SCT有助于取得良好的结果。