Cell-based Therapy for Acute Respiratory Distress Syndrome Biology and Potential Therapeutic Value

被引:184
作者
Laffey, John G. [1 ,2 ]
Matthay, Michael A. [3 ,4 ]
机构
[1] Univ Toronto, St Michaels Hosp, Dept Anesthesia, Toronto, ON, Canada
[2] Univ Toronto, St Michaels Hosp, Keenan Res Ctr Biomed Sci, Toronto, ON, Canada
[3] Univ Calif San Francisco, Cardiovasc Res Inst, Dept Med, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Cardiovasc Res Inst, Dept Anesthesia, San Francisco, CA 94143 USA
基金
美国国家卫生研究院;
关键词
mesenchymal stromal cells; pulmonary edema; acute lung injury; MESENCHYMAL STEM-CELLS; ACUTE LUNG INJURY; ALVEOLAR FLUID CLEARANCE; STROMAL CELLS; BONE-MARROW; IN-VITRO; MITOCHONDRIAL TRANSFER; INTERNATIONAL-SOCIETY; PART; MICROVESICLES;
D O I
10.1164/rccm.201701-0107CP
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
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.
引用
收藏
页码:266 / 273
页数:8
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