Laffey John G, Matthay Michael A
1 Department of Anesthesia and.
2 Keenan Research Centre for Biomedical Science, St. Michael's Hospital, University of Toronto, Toronto, Ontario, Canada; and.
Am J Respir Crit Care Med. 2017 Aug 1;196(3):266-273. doi: 10.1164/rccm.201701-0107CP.
On the basis of several preclinical studies, cell-based therapy has emerged as a potential new therapeutic for acute respiratory distress syndrome (ARDS). Of the various cell-based therapy options, mesenchymal stem/stromal cells (MSCs) from bone marrow, adipose tissue, and umbilical cord have the most experimental data to support their potential efficacy for lung injury from both infectious and noninfectious causes. Mechanistically, MSCs exert their beneficial effects by release of paracrine factors, microvesicles, and transfer of mitochondria, all of which have antiinflammatory and pro-resolving effects on injured lung endothelium and alveolar epithelium, including enhancing the resolution of pulmonary edema by up-regulating sodium-dependent alveolar fluid clearance. MSCs also have antimicrobial effects mediated by release of antimicrobial factors and by up-regulating monocyte/macrophage phagocytosis. Phase 2a clinical trials to establish safety in ARDS are in progress, and two phase 1 trials did not report any serious adverse events. Several issues need further study, including: determining the optimal methods for large-scale production, reconstitution of cryopreserved cells for clinical use, defining cell potency assays, and determining the therapeutic potential of conditioned media derived from MSCs. Because ARDS is a heterogeneous syndrome, targeting MSCs to patients with ARDS with a more hyperinflammatory endotype may further enhance their potential for efficacy.
基于多项临床前研究,细胞疗法已成为急性呼吸窘迫综合征(ARDS)一种潜在的新治疗方法。在各种基于细胞的治疗选择中,来自骨髓、脂肪组织和脐带的间充质干/基质细胞(MSCs)拥有最多的实验数据来支持其对感染性和非感染性原因导致的肺损伤的潜在疗效。从机制上讲,MSCs通过释放旁分泌因子、微泡以及线粒体转移发挥其有益作用,所有这些对受损的肺内皮细胞和肺泡上皮细胞都具有抗炎和促消退作用,包括通过上调钠依赖性肺泡液体清除来增强肺水肿的消退。MSCs还具有由抗菌因子释放和上调单核细胞/巨噬细胞吞噬作用介导的抗菌作用。在ARDS中建立安全性的2a期临床试验正在进行中,两项1期试验未报告任何严重不良事件。几个问题需要进一步研究,包括:确定大规模生产的最佳方法、用于临床使用的冷冻保存细胞的复溶、定义细胞效力测定方法以及确定源自MSCs的条件培养基的治疗潜力。由于ARDS是一种异质性综合征,将MSCs靶向具有更高度炎症内型的ARDS患者可能会进一步提高其疗效潜力。