Matsushima Satoru, Kobayashi Ryoji, Hori Daiki, Yanagi Masato, Kodama Koya, Sano Hirozumi, Suzuki Daisuke, Kobayashi Kunihiko
Department of Hematology/Oncology for Children and Adolescents, Sapporo Hokuyu Hospital, Japan.
Blood Cell Ther. 2022 Jan 28;5(1):27-30. doi: 10.31547/bct-2021-013. eCollection 2022 Feb 25.
Administration of mesenchymal stromal cells (MSCs) represents a promising therapy for steroid-resistant acute graft-versus-host disease (aGVHD). However, its efficacy in pediatric patients with steroid-dependent aGVHD remains unclear, given the paucity of studies performed in children. In addition, the duration between the onset of aGVHD and MSC therapy is reportedly critical; a delay in MSC administration negatively impacts overall survival and response rate. Herein, we describe a case of a 14-year-old girl with steroid-dependent aGVHD who was successfully treated with MSCs following a prolonged duration from aGVHD diagnosis. The patient was diagnosed with T-cell lymphoblastic leukemia with central nervous system involvement and underwent cord blood transplantation (CBT). She developed severe gastrointestinal aGVHD on day +14 after CBT and was treated with a steroid; however, her aGVHD was repeatedly exacerbated upon tapering the steroid, later complicated by diabetic ketoacidosis. We eventually implemented MSC therapy for steroid-dependent aGVHD on day +109 after CBT. She rapidly responded to therapy, and her aGVHD was ameliorated even with steroid tapering. This case exemplifies the potential role of MSCs in treating pediatric patients with steroid-dependent aGVHD or late aGVHD.
间充质基质细胞(MSCs)给药是治疗类固醇难治性急性移植物抗宿主病(aGVHD)的一种有前景的疗法。然而,鉴于针对儿童进行的研究较少,其在类固醇依赖型aGVHD患儿中的疗效仍不明确。此外,据报道,aGVHD发病与MSC治疗之间的时间间隔至关重要;延迟给予MSC会对总生存期和缓解率产生负面影响。在此,我们描述了一例14岁类固醇依赖型aGVHD女孩的病例,该患者在aGVHD诊断后经过较长时间才成功接受了MSCs治疗。该患者被诊断为伴有中枢神经系统受累的T细胞淋巴细胞白血病,并接受了脐血移植(CBT)治疗。她在CBT后第14天出现了严重的胃肠道aGVHD,并接受了类固醇治疗;然而,在逐渐减少类固醇用量时,她的aGVHD反复加重,后来并发糖尿病酮症酸中毒。我们最终在CBT后第109天对类固醇依赖型aGVHD实施了MSC治疗法。她对治疗迅速产生反应,并即使在逐渐减少类固醇用量的情况下,其aGVHD也得到了改善。该病例例证了MSCs在治疗类固醇依赖型aGVHD或晚期aGVHD患儿中的潜在作用。