Stem cell therapy for COVID-19 and other respiratory diseases: Global trends of clinical trials

被引:17
作者
Ji, Hong-Long [1 ,2 ]
Liu, Cong [3 ]
Zhao, Run-Zhen [1 ]
机构
[1] Univ Texas Tyler, Hlth Sci Ctr Tyler, Dept Cellular & Mol Biol, Tyler, TX 75708 USA
[2] Univ Texas Tyler, Hlth Sci Ctr Tyler, Texas Lung Injury Inst, Tyler, TX 75708 USA
[3] Southern Univ Sci & Technol, Sch Med, Shenzhen 518000, Guangdong, Peoples R China
关键词
Pulmonary diseases; COVID-19; Cell therapy; Exosomes; Clinical trial; PULMONARY ARTERIAL-HYPERTENSION; MESENCHYMAL STROMAL CELLS; ENDOTHELIAL PROGENITOR CELLS; BONE-MARROW; PHASE-I; BRONCHOPULMONARY DYSPLASIA; TRANSPLANTATION; DELIVERY; SAFETY; MECHANISMS;
D O I
10.4252/wjsc.v12.i6.471
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Respiratory diseases, including coronavirus disease 2019 and chronic obstructive pulmonary disease (COPD), are leading causes of global fatality. There are no effective and curative treatments, but supportive care only. Cell therapy is a promising therapeutic strategy for refractory and unmanageable pulmonary illnesses, as proved by accumulating preclinical studies. Stem cells consist of totipotent, pluripotent, multipotent, and unipotent cells with the potential to differentiate into cell types requested for repair. Mesenchymal stromal cells, endothelial progenitor cells, peripheral blood stem cells, and lung progenitor cells have been applied to clinical trials. To date, the safety and feasibility of stem cell and extracellular vesicles administration have been confirmed by numerous phase I/II trials in patients with COPD, acute respiratory distress syndrome, bronchial dysplasia, idiopathic pulmonary fibrosis, pulmonary artery hypertension, and silicosis. Five routes and a series of doses have been tested for tolerance and advantages of different regimes. In this review, we systematically summarize the global trends for the cell therapy of common airway and lung diseases registered for clinical trials. The future directions for both new clinical trials and preclinical studies are discussed.
引用
收藏
页码:471 / 480
页数:10
相关论文
共 69 条
[21]   Mesenchymal stem cells: are we ready for clinical application in transplantation and tissue regeneration? [J].
Hoogduijn, Martin J. ;
Dor, Frank J. M. F. .
FRONTIERS IN IMMUNOLOGY, 2013, 4
[22]   The molecular targets of approved treatments for pulmonary arterial hypertension [J].
Humbert, Marc ;
Ghofrani, Hossein-Ardeschir .
THORAX, 2016, 71 (01) :73-83
[23]   Mitochondrial transfer from bone-marrow-derived stromal cells to pulmonary alveoli protects against acute lung injury [J].
Islam, Mohammad Naimul ;
Das, Shonit R. ;
Emin, Memet T. ;
Wei, Michelle ;
Sun, Li ;
Westphalen, Kristin ;
Rowlands, David J. ;
Quadri, Sadiqa K. ;
Bhattacharya, Sunita ;
Bhattacharya, Jahar .
NATURE MEDICINE, 2012, 18 (05) :759-U153
[24]   ELEVATED PLASMIN(OGEN) AS A COMMON RISK FACTOR FOR COVID-19 SUSCEPTIBILITY [J].
Ji, Hong-Long ;
Zhao, Runzhen ;
Matalon, Sadis ;
Matthay, Michael A. .
PHYSIOLOGICAL REVIEWS, 2020, 100 (03) :1065-1075
[25]   Comparative Analysis of Human Mesenchymal Stem Cells from Bone Marrow, Adipose Tissue, and Umbilical Cord Blood as Sources of Cell Therapy [J].
Jin, Hye Jin ;
Bae, Yun Kyung ;
Kim, Miyeon ;
Kwon, Soon-Jae ;
Jeon, Hong Bae ;
Choi, Soo Jin ;
Kim, Seong Who ;
Yang, Yoon Sun ;
Oh, Wonil ;
Chang, Jong Wook .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2013, 14 (09) :17986-18001
[26]   Integrating Non-human Primate, Human, and Mathematical Studies to Determine the Influence of BCG Timing on H56 Vaccine Outcomes [J].
Joslyn, Louis R. ;
Pienaar, Elsje ;
DiFazio, Robert M. ;
Suliman, Sara ;
Kagina, Benjamin M. ;
Flynn, JoAnne L. ;
Scriba, Thomas J. ;
Linderman, Jennifer J. ;
Kirschner, Denise E. .
FRONTIERS IN MICROBIOLOGY, 2018, 9
[27]   Cell-based Therapy for Acute Respiratory Distress Syndrome Biology and Potential Therapeutic Value [J].
Laffey, John G. ;
Matthay, Michael A. .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2017, 196 (03) :266-273
[28]   Mesenchymal stem cell exosomes [J].
Lai, Ruenn Chai ;
Yeo, Ronne Wee Yeh ;
Lim, Sai Kiang .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2015, 40 :82-88
[29]   Exosome secreted by MSC reduces myocardial ischemia/reperfusion injury [J].
Lai, Ruenn Chai ;
Arslan, Fatih ;
Lee, May May ;
Sze, Newman Siu Kwan ;
Choo, Andre ;
Chen, Tian Sheng ;
Salto-Tellez, Manuel ;
Timmers, Leo ;
Lee, Chuen Neng ;
El Oakley, Reida Menshawe ;
Pasterkamp, Gerard ;
de Kleijn, Dominique P. V. ;
Lim, Sai Kiang .
STEM CELL RESEARCH, 2010, 4 (03) :214-222
[30]   Immunomodulatory effects of fetal and adult mesenchymal stem cells [J].
Le Blanc, K .
CYTOTHERAPY, 2003, 5 (06) :485-489