Senior Department of Hematology, The Fifth Medical Center of Chinese People's Liberation Army (PLA) General Hospital, Beijing, China.
Front Immunol. 2024 Aug 15;15:1436653. doi: 10.3389/fimmu.2024.1436653. eCollection 2024.
INTRODUCTION: Mesenchymal stromal cells (MSCs) have been extensively studied as a potential treatment for steroid refractory acute graft-versus-host disease (aGVHD). However, the majority of clinical trials have focused on bone marrow-derived MSCs. METHODS: In this study, we report the outcomes of 86 patients with grade III-IV (82.6% grade IV) steroid refractory aGVHD who were treated with human umbilical cord-derived mesenchymal stromal cells (UC-MSCs). The patient cohort included 17 children and 69 adults. All patients received intravenous infusions of UC-MSCs at a dose of 1 × 106 cells per kg body weight, with a median of 4 infusions (ranging from 1 to 16). RESULTS: The median time between the onset of aGVHD and the first infusion of UC-MSCs was 7 days (ranging from 3 to 88 days). At day 28, the overall response (OR) rate was 52.3%. Specifically, 24 patients (27.9%) achieved complete remission, while 21 (24.4%) exhibited partial remission. The estimated survival probability at 100 days was 43.7%. Following a median follow-up of 108 months (ranging from 61 to 159 months), the survival rate was approximately 11.6% (10/86). Patients who developed acute lower GI tract and liver GVHD exhibited poorer OR rates at day 28 compared to those with only acute lower GI tract GVHD (22.2% vs. 58.8%; p= 0.049). No patient experienced serious adverse events. DISCUSSION: These finding suggest that UC-MSCs are safe and effective in both children and adults with steroid refractory aGVHD. UC-MSCs could be considered as a feasible treatment option for this challenging conditon. (NCT01754454).
简介:间充质基质细胞(MSCs)已被广泛研究作为治疗类固醇难治性急性移植物抗宿主病(aGVHD)的潜在方法。然而,大多数临床试验都集中在骨髓来源的 MSCs 上。
方法:在这项研究中,我们报告了 86 例 III-IV 级(82.6%为 IV 级)类固醇难治性 aGVHD 患者接受人脐带间充质基质细胞(UC-MSCs)治疗的结果。患者队列包括 17 名儿童和 69 名成人。所有患者均接受 1×106 个细胞/公斤体重的静脉输注 UC-MSCs,中位数为 4 次输注(范围为 1 至 16 次)。
结果:aGVHD 发病至首次输注 UC-MSCs 的中位时间为 7 天(范围为 3 至 88 天)。在第 28 天,总反应(OR)率为 52.3%。具体来说,24 例(27.9%)患者完全缓解,21 例(24.4%)患者部分缓解。100 天的估计生存率为 43.7%。中位随访 108 个月(范围为 61 至 159 个月)后,生存率约为 11.6%(10/86)。发生急性下胃肠道和肝脏 GVHD 的患者在第 28 天的 OR 率低于仅发生急性下胃肠道 GVHD 的患者(22.2% vs. 58.8%;p=0.049)。没有患者发生严重不良事件。
讨论:这些发现表明 UC-MSCs 对类固醇难治性 aGVHD 的儿童和成人均安全有效。UC-MSCs 可被视为治疗这种具有挑战性疾病的可行选择。(NCT01754454)
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