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1
Cryopreserved, Xeno-Free Human Umbilical Cord Mesenchymal Stromal Cells Reduce Lung Injury Severity and Bacterial Burden in Rodent Escherichia coli-Induced Acute Respiratory Distress Syndrome.冻存、无动物源的人脐带间充质基质细胞减轻啮齿动物大肠埃希菌诱导的急性呼吸窘迫综合征肺损伤严重程度和细菌负荷。
Crit Care Med. 2017 Feb;45(2):e202-e212. doi: 10.1097/CCM.0000000000002073.
2
Mesenchymal stromal cell treatment prevents H9N2 avian influenza virus-induced acute lung injury in mice.间充质基质细胞治疗可预防H9N2禽流感病毒诱导的小鼠急性肺损伤。
Stem Cell Res Ther. 2016 Oct 28;7(1):159. doi: 10.1186/s13287-016-0395-z.
3
Acute Respiratory Distress Syndrome Subphenotypes Respond Differently to Randomized Fluid Management Strategy.急性呼吸窘迫综合征的亚型对随机液体管理策略反应不同。
Am J Respir Crit Care Med. 2017 Feb 1;195(3):331-338. doi: 10.1164/rccm.201603-0645OC.
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Acute Respiratory Distress Syndrome Measurement Error. Potential Effect on Clinical Study Results.急性呼吸窘迫综合征测量误差。对临床研究结果的潜在影响。
Ann Am Thorac Soc. 2016 Jul;13(7):1123-8. doi: 10.1513/AnnalsATS.201601-072OC.
5
Mitochondrial Transfer via Tunneling Nanotubes is an Important Mechanism by Which Mesenchymal Stem Cells Enhance Macrophage Phagocytosis in the In Vitro and In Vivo Models of ARDS.通过隧道纳米管进行线粒体转移是间充质干细胞在急性呼吸窘迫综合征的体外和体内模型中增强巨噬细胞吞噬作用的重要机制。
Stem Cells. 2016 Aug;34(8):2210-23. doi: 10.1002/stem.2372. Epub 2016 Apr 29.
6
Human mesenchymal stromal cells reduce influenza A H5N1-associated acute lung injury in vitro and in vivo.人间充质基质细胞在体外和体内均可减轻甲型H5N1流感相关的急性肺损伤。
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7
Epidemiology, Patterns of Care, and Mortality for Patients With Acute Respiratory Distress Syndrome in Intensive Care Units in 50 Countries.全球 50 个国家重症监护病房急性呼吸窘迫综合征患者的流行病学、治疗模式和死亡率。
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8
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10
International Society for Cellular Therapy perspective on immune functional assays for mesenchymal stromal cells as potency release criterion for advanced phase clinical trials.国际细胞治疗协会关于间充质基质细胞免疫功能测定作为晚期临床试验效力释放标准的观点。
Cytotherapy. 2016 Feb;18(2):151-9. doi: 10.1016/j.jcyt.2015.11.008. Epub 2015 Dec 23.

急性呼吸窘迫综合征五十年研究。急性呼吸窘迫综合征的细胞疗法。生物学及潜在治疗价值。

Fifty Years of Research in ARDS. Cell-based Therapy for Acute Respiratory Distress Syndrome. Biology and Potential Therapeutic Value.

作者信息

Laffey John G, Matthay Michael A

机构信息

1 Department of Anesthesia and.

2 Keenan Research Centre for Biomedical Science, St. Michael's Hospital, University of Toronto, Toronto, Ontario, Canada; and.

出版信息

Am J Respir Crit Care Med. 2017 Aug 1;196(3):266-273. doi: 10.1164/rccm.201701-0107CP.

DOI:10.1164/rccm.201701-0107CP
PMID:28306336
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5549868/
Abstract

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.

摘要

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。