Sinclair Centre for Regenerative Medicine, Ottawa Hospital Research Institute, Ottawa, ON, Canada.
Department of Medicine, University of Toronto, Toronto, ON, Canada.
Crit Care Med. 2019 Jul;47(7):918-925. doi: 10.1097/CCM.0000000000003657.
Cellular Immunotherapy for Septic Shock is the first-in-human clinical trial evaluating allogeneic mesenchymal stem/stromal cells in septic shock patients. Here, we sought to determine whether plasma cytokine profiles may provide further information into the safety and biological effects of mesenchymal stem/stromal cell treatment, as no previous study has conducted a comprehensive analysis of circulating cytokine levels in critically ill patients treated with mesenchymal stem/stromal cells.
Phase 1 dose-escalation trial.
The interventional cohort (n = 9) of septic shock patients received a single dose of 0.3, 1.0, or 3.0 million mesenchymal stem/stromal cells/kg body weight (n = 3 per dose). The observational cohort received no mesenchymal stem/stromal cells (n = 21).
Allogeneic bone marrow-derived mesenchymal stem/stromal cells.
Serial plasma samples were collected at study baseline prior to mesenchymal stem/stromal cell infusion (0 hr), 1 hour, 4 hours, 12 hours, 24 hours, and 72 hours after mesenchymal stem/stromal cell infusion/trial enrollment. Forty-nine analytes comprised mostly of cytokines along with several biomarkers were measured. We detected no significant elevations in a broad range of pro-inflammatory cytokines and biomarkers between the interventional and observational cohorts. Stratification of the interventional cohort by mesenchymal stem/stromal cell dose further revealed patient-specific and dose-dependent perturbations in cytokines, including an early but transient dampening of pro-inflammatory cytokines (e.g., interleukin-1β, interleukin-2, interleukin-6, interleukin-8, and monocyte chemoattractant protein 1), suggesting that mesenchymal stem/stromal cell treatment may alter innate immune responses and underlying sepsis biology.
A single infusion of up to 3 million cells/kg of allogeneic mesenchymal stem/stromal cells did not exacerbate elevated cytokine levels in plasma of septic shock patients, consistent with a safe response. These data also offer insight into potential biological mechanisms of mesenchymal stem/stromal cell treatment and support further investigation in larger randomized controlled trials.
细胞免疫疗法治疗感染性休克是首个评估同种异体间充质干细胞治疗感染性休克患者的人体临床试验。在这里,我们旨在确定血浆细胞因子谱是否可以提供关于间充质干细胞治疗安全性和生物学效应的更多信息,因为之前没有研究对接受间充质干细胞治疗的危重病患者进行循环细胞因子水平的综合分析。
1 期剂量递增试验。
干预队列(n = 9)中的感染性休克患者接受了 0.3、1.0 或 3.0 百万个间充质干细胞/公斤体重的单次剂量(每个剂量 n = 3)。观察队列未接受间充质干细胞治疗(n = 21)。
同种异体骨髓来源的间充质干细胞。
在间充质干细胞输注/试验入组前的研究基线(0 小时)、输注后 1 小时、4 小时、12 小时、24 小时和 72 小时收集了连续的血浆样本。共测量了 49 种分析物,主要是细胞因子和几种生物标志物。我们没有在干预和观察队列之间检测到广泛的促炎细胞因子和生物标志物的显著升高。对干预队列的分层进一步显示,细胞因子存在患者特异性和剂量依赖性改变,包括促炎细胞因子(例如白细胞介素-1β、白细胞介素-2、白细胞介素-6、白细胞介素-8 和单核细胞趋化蛋白 1)的早期但短暂的抑制,这表明间充质干细胞治疗可能改变固有免疫反应和潜在的败血症生物学。
单次输注高达 300 万个细胞/公斤的同种异体间充质干细胞不会加剧感染性休克患者血浆中升高的细胞因子水平,这与安全反应一致。这些数据还为间充质干细胞治疗的潜在生物学机制提供了深入了解,并支持在更大的随机对照试验中进一步研究。