@article{1567dab304d24a93811d85f43387e596,
title = "Cell-based therapy to reduce mortality from COVID-19: Systematic review and meta-analysis of human studies on acute respiratory distress syndrome",
abstract = "Severe cases of COVID-19 infection, often leading to death, have been associated with variants of acute respiratory distress syndrome (ARDS). Cell therapy with mesenchymal stromal cells (MSCs) is a potential treatment for COVID-19 ARDS based on preclinical and clinical studies supporting the concept that MSCs modulate the inflammatory and remodeling processes and restore alveolo-capillary barriers. The authors performed a systematic literature review and random-effects meta-analysis to determine the potential value of MSC therapy for treating COVID-19-infected patients with ARDS. Publications in all languages from 1990 to March 31, 2020 were reviewed, yielding 2691 studies, of which nine were included. MSCs were intravenously or intratracheally administered in 117 participants, who were followed for 14 days to 5 years. All MSCs were allogeneic from bone marrow, umbilical cord, menstrual blood, adipose tissue, or unreported sources. Combined mortality showed a favorable trend but did not reach statistical significance. No related serious adverse events were reported and mild adverse events resolved spontaneously. A trend was found of improved radiographic findings, pulmonary function (lung compliance, tidal volumes, PaO2/FiO2 ratio, alveolo-capillary injury), and inflammatory biomarker levels. No comparisons were made between MSCs of different sources.",
keywords = "COVID-19, acute respiratory distress syndrome, mesenchymal stromal cells, mortality, systematic review",
author = "Wenchun Qu and Zhen Wang and Hare, {Joshua M.} and Guojun Bu and Mallea, {Jorge M.} and Pascual, {Jorge M.} and Caplan, {Arnold I.} and Joanne Kurtzberg and Zubair, {Abba C.} and Eva Kubrova and Erica Engelberg-Cook and Tarek Nayfeh and Shah, {Vishal P.} and Hill, {James C.} and Wolf, {Michael E.} and Prokop, {Larry J.} and Murad, {M. Hassan} and Sanfilippo, {Fred P.}",
note = "Funding Information: W. Q., J. M. H., J. K., and J. M. M. reported roles as principal investigators of MSC trials. F. P. S. is a paid consultant as Medical Director of The Marcus Foundation, which funds numerous clinical trials involving MSCs. J. M. M. is an unpaid Scientific Advisor for BreStem Therapeutics. J. M. H. reported having a patent for cardiac cell‐based therapy, holds equity in Vestion, Inc., and maintains a professional relationship with Vestion, Inc. as a consultant and member of the Board of Directors and Scientific Advisory Board; J. M. H. is also the Chief Scientific Officer, a compensated consultant and advisory board member, for Longeveron and holds equity in Longeveron; J. M. H. is the coinventor of intellectual property licensed to Longeveron. J. M. H. declared inventor or patent holder and research funding from Longeveron, Heart Genomics; advisory role and research funding with Vestion; research funding from NHLBI. J. K. declare Intellectual property rights with IDF, hCT‐MSC for treatment of ASD, HIE, CP; NMDP Scientific Advisor; Celularity SAB; research funding from the Marcus Foundation, NIH, HRSA; leadership position with Istari—CMO (spouse). F. P. S. declared advisory role with the Marcus Foundation, Neuvana, Radix Health. The other authors indicated no potential conflicts of interest. Publisher Copyright: {\textcopyright} 2020 The Authors. STEM CELLS TRANSLATIONAL MEDICINE published by Wiley Periodicals, Inc. on behalf of AlphaMed Press",
year = "2020",
month = sep,
day = "1",
doi = "10.1002/sctm.20-0146",
language = "English (US)",
volume = "9",
pages = "1007--1022",
journal = "Stem Cells Translational Medicine",
issn = "2157-6564",
publisher = "AlphaMed Press",
number = "9",
}