Efficacy of MSC in Patients with Severe COVID-19: Analysis of the Literature and a Case Study

被引:12
作者
Grumet, Martin [1 ]
Sherman, Jason [1 ]
Dorf, Barry S. [1 ,2 ]
机构
[1] Rutgers State Univ, Dept Cell Biol & Neurosci, WM Keck Ctr Collaborat Neurosci, Rutgers Stem Cell Res Ctr, Piscataway, NJ USA
[2] North Shore Univ Hosp, Dept Med, 300 Community Dr, Manhasset, NY USA
关键词
COVID; mesenchymal stromal cells; cytokine storm; clinical trials; ARDS; COVID-19; MESENCHYMAL STEM-CELLS; STROMAL CELLS; MORTALITY; DISEASE;
D O I
10.1093/stcltm/szac067
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Patients with severe COVID-19 experience cytokine storm, an uncontrolled upregulation of pro-inflammatory cytokines, which if unresolved leads to acute respiratory distress syndrome (ARDS), organ damage, and death. Treatments with mesenchymal stromal cells (MSC) [Viswanathan S, Shi Y, Galipeau J, et al. Mesenchymal stem versus stromal cells: International Society for Cell & Gene Therapy Mesenchymal Stromal Cell committee position statement on nomenclature. Cytotherapy. 2019;21:1019-1024] appear to be effective in reducing morbidity and mortality. MSC respond to pro-inflammatory cytokines by releasing anti-inflammatory factors and mobilizing immune cells. We analyzed 82 COVID-19 clinical trials registered at ClinicalTrials.gov to determine MSC dosing, routes of administration, and outcome measures. Nearly all trials described the use of intravenous delivery with most doses ranging between 50 and 125 million MSC/treatment, which overlaps with a minimal effective dose range that we described previously. We also searched the literature to analyze clinical trial reports that used MSC to treat COVID-19. MSC were found to improve survival and oxygenation, increase discharge from intensive care units and hospitals, and reduce levels of pro-inflammatory markers. We report on a 91-year-old man with severe COVID-19 who responded rapidly to MSC treatment with transient reductions in several pro-inflammatory markers and delayed improvement in oxygenation. The results suggest that frequent monitoring of pro-inflammatory markers for severe COVID-19 will provide improved treatment guidelines by determining relationships between cytokine storms and ARDS. We propose that markers for cytokine storm are leading indicators for ARDS and that measurement of cytokines will indicate earlier treatment with MSC than is performed now for ARDS in severe COVID-19.
引用
收藏
页码:1103 / 1112
页数:10
相关论文
共 49 条
[1]  
Adams Paul, 2008, Gastroenterol Hepatol (N Y), V4, P333
[2]   Immunomodulatory therapy for the management of severe COVID-19. Beyond the anti-viral therapy: A comprehensive review [J].
Alijotas-Reig, Jaume ;
Esteve-Valverde, Enrique ;
Belizna, Cristina ;
Selva-O'Callaghan, Albert ;
Pardos-Gea, Josep ;
Quintana, Angela ;
Mekinian, Arsene ;
Anunciacion-Llunell, Ariadna ;
Miro-Mur, Francesc .
AUTOIMMUNITY REVIEWS, 2020, 19 (07)
[3]   COVID-19: Discovery, diagnostics and drug development [J].
Asselah, Tarik ;
Durantel, David ;
Pasmant, Eric ;
Lau, George ;
Schinazi, Raymond F. .
JOURNAL OF HEPATOLOGY, 2021, 74 (01) :168-184
[4]  
Barkama Ravit, 2020, Crit Care Explor, V2, pe0207, DOI 10.1097/CCE.0000000000000207
[5]   Encapsulated Mesenchymal Stromal Cells for In vivo Transplantation [J].
Barminko, Jeffrey ;
Kim, Jae Hwan ;
Otsuka, Seiji ;
Gray, Andrea ;
Schloss, Rene ;
Grumet, Martin ;
Yarmush, Martin L. .
BIOTECHNOLOGY AND BIOENGINEERING, 2011, 108 (11) :2747-2758
[6]   Mesenchymal stromal cells to fight SARS-CoV-2: Taking advantage of a pleiotropic therapy [J].
Barros, Ines ;
Silva, Antonio ;
de Almeida, Luis Pereirad ;
Miranda, Catarina Oliveira .
CYTOKINE & GROWTH FACTOR REVIEWS, 2021, 58 :114-133
[7]   Safety and efficacy of multipotent adult progenitor cells in acute respiratory distress syndrome (MUST-ARDS): a multicentre, randomised, double-blind, placebo-controlled phase 1/2 trial [J].
Bellingan, G. ;
Jacono, F. ;
Bannard-Smith, J. ;
Brealey, D. ;
Meyer, N. ;
Thickett, D. ;
Young, D. ;
Bentley, A. ;
McVerry, B. J. ;
Wunderink, R. G. ;
Doerschug, K. C. ;
Summers, C. ;
Rojas, M. ;
Ting, A. ;
Jenkins, E. D. .
INTENSIVE CARE MEDICINE, 2022, 48 (01) :36-44
[8]   Pulmonary Passage is a Major Obstacle for Intravenous Stem Cell Delivery: The Pulmonary First-Pass Effect [J].
Fischer, Uwe M. ;
Harting, Matthew T. ;
Jimenez, Fernando ;
Monzon-Posadas, Werner O. ;
Xue, Hasen ;
Savitz, Sean I. ;
Laine, Glen A. ;
Cox, Charles S., Jr. .
STEM CELLS AND DEVELOPMENT, 2009, 18 (05) :683-691
[9]   Mesenchymal stromal cell variables influencing clinical potency: the impact of viability, fitness, route of administration and host predisposition [J].
Galipeau, Jacques ;
Krampera, Mauro ;
Leblanc, Katarina ;
Nolta, Jan A. ;
Phinney, Donald G. ;
Shi, Yufang ;
Tarte, Karin ;
Viswanathan, Sowmya ;
Martin, Ivan .
CYTOTHERAPY, 2021, 23 (05) :368-372
[10]   Differential Co-Expression Network Analysis Reveals Key Hub-High Traffic Genes as Potential Therapeutic Targets for COVID-19 Pandemic [J].
Hasankhani, Aliakbar ;
Bahrami, Abolfazl ;
Sheybani, Negin ;
Aria, Behzad ;
Hemati, Behzad ;
Fatehi, Farhang ;
Farahani, Hamid Ghaem Maghami ;
Javanmard, Ghazaleh ;
Rezaee, Mahsa ;
Kastelic, John P. ;
Barkema, Herman W. .
FRONTIERS IN IMMUNOLOGY, 2021, 12