Department of Pediatrics and Developmental Biology, Tokyo Medical and Dental University, 1-5-45 Yushima, Bunkyo-ku, Tokyo, Japan.
Hereditary Disorder Working Group of the Japanese Society for Transplantation and Cellular Therapy, 1-1-20 Daiko-Minami, Higashi-ku, Nagoya, Aichi, Japan.
J Clin Immunol. 2021 Nov;41(8):1865-1877. doi: 10.1007/s10875-021-01112-5. Epub 2021 Aug 27.
Hematopoietic cell transplantation (HCT) is a curative therapy for patients with severe combined immunodeficiency (SCID). Here, we conducted a nationwide study to assess the outcome of SCID patients after HCT in Japan.
A cohort of 181 SCID patients undergoing their first allogeneic HCT in 1974-2016 was studied by using the Japanese national database (Transplant Registry Unified Management Program, TRUMP).
The 10-year overall survival (OS) of the patients who received HCT in 2006-2016 was 67%. Umbilical cord blood (UCB) transplantation was performed in 81 patients (45%). The outcomes of HCT from HLA-matched UCB (n = 21) and matched sibling donors (n = 22) were comparable, including 10-year OS (91% vs. 91%), neutrophil recovery (cumulative incidence at 30 days, 89% vs. 100%), and platelet recovery (cumulative incidence at 60 days, 89% vs. 100%). Multivariate analysis of the patients who received HCT in 2006-2016 demonstrated that the following factors were associated with poor OS: bacterial or fungal infection at HCT (hazard ratio (HR): 3.8, P = 0.006), cytomegalovirus infection prior to HCT (HR: 9.4, P = 0.03), ≥ 4 months of age at HCT (HR: 25.5, P = 0.009), and mismatched UCB (HR: 19.8, P = 0.01).
We showed the potential of HLA-matched UCB as a donor source with higher priority for SCID patients. We also demonstrated that early age at HCT without active infection is critical for a better prognosis, highlighting the importance of newborn screening for SCID.
造血细胞移植(HCT)是治疗严重联合免疫缺陷(SCID)患者的一种有治愈可能的疗法。在此,我们通过日本全国性数据库(移植登记统一管理计划,TRUMP)对 1974 年至 2016 年间接受首次异基因 HCT 的 181 例 SCID 患者的结局进行了研究。
通过日本全国性数据库(移植登记统一管理计划,TRUMP)对 1974 年至 2016 年间接受首次异基因 HCT 的 181 例 SCID 患者进行了研究。
2006 年至 2016 年接受 HCT 的患者的 10 年总生存率(OS)为 67%。81 例患者(45%)接受了脐带血(UCB)移植。HLA 匹配的 UCB(n=21)和匹配的同胞供者(n=22)来源的 HCT 结果相当,包括 10 年 OS(91% vs. 91%)、中性粒细胞恢复(第 30 天累积发生率,89% vs. 100%)和血小板恢复(第 60 天累积发生率,89% vs. 100%)。对 2006 年至 2016 年接受 HCT 的患者进行多变量分析显示,以下因素与较差的 OS 相关:HCT 时发生细菌或真菌感染(风险比(HR):3.8,P=0.006)、HCT 前发生巨细胞病毒感染(HR:9.4,P=0.03)、HCT 时年龄≥4 个月(HR:25.5,P=0.009)和 UCB 不匹配(HR:19.8,P=0.01)。
我们表明了 HLA 匹配的 UCB 作为供者来源的潜力,这种来源应优先用于 SCID 患者。我们还表明,HCT 时年龄较小且无活动性感染是更好预后的关键,这凸显了 SCID 新生儿筛查的重要性。