Cell-based therapy to reduce mortality from COVID-19: Systematic review and meta-analysis of human studies on acute respiratory distress syndrome.

dc.contributor.author

Qu, Wenchun

dc.contributor.author

Wang, Zhen

dc.contributor.author

Hare, Joshua M

dc.contributor.author

Bu, Guojun

dc.contributor.author

Mallea, Jorge M

dc.contributor.author

Pascual, Jorge M

dc.contributor.author

Caplan, Arnold I

dc.contributor.author

Kurtzberg, Joanne

dc.contributor.author

Zubair, Abba C

dc.contributor.author

Kubrova, Eva

dc.contributor.author

Engelberg-Cook, Erica

dc.contributor.author

Nayfeh, Tarek

dc.contributor.author

Shah, Vishal P

dc.contributor.author

Hill, James C

dc.contributor.author

Wolf, Michael E

dc.contributor.author

Prokop, Larry J

dc.contributor.author

Murad, M Hassan

dc.contributor.author

Sanfilippo, Fred P

dc.date.accessioned

2022-03-23T15:11:34Z

dc.date.available

2022-03-23T15:11:34Z

dc.date.issued

2020-09

dc.date.updated

2022-03-23T15:11:33Z

dc.description.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.

dc.identifier.issn

2157-6564

dc.identifier.issn

2157-6580

dc.identifier.uri

https://hdl.handle.net/10161/24576

dc.language

eng

dc.publisher

Oxford University Press (OUP)

dc.relation.ispartof

Stem cells translational medicine

dc.relation.isversionof

10.1002/sctm.20-0146

dc.subject

Lung

dc.subject

Mesenchymal Stem Cells

dc.subject

Humans

dc.subject

Pneumonia, Viral

dc.subject

Coronavirus Infections

dc.subject

Cytokines

dc.subject

Mesenchymal Stem Cell Transplantation

dc.subject

Pandemics

dc.subject

Cell- and Tissue-Based Therapy

dc.subject

Betacoronavirus

dc.subject

Respiratory Distress Syndrome

dc.subject

COVID-19

dc.subject

SARS-CoV-2

dc.title

Cell-based therapy to reduce mortality from COVID-19: Systematic review and meta-analysis of human studies on acute respiratory distress syndrome.

dc.type

Journal article

duke.contributor.orcid

Kurtzberg, Joanne|0000-0002-3370-0703

pubs.begin-page

1007

pubs.end-page

1022

pubs.issue

9

pubs.organisational-group

Duke

pubs.organisational-group

School of Medicine

pubs.organisational-group

Clinical Science Departments

pubs.organisational-group

Institutes and Centers

pubs.organisational-group

Pathology

pubs.organisational-group

Pediatrics

pubs.organisational-group

Duke Cancer Institute

pubs.organisational-group

Institutes and Provost's Academic Units

pubs.organisational-group

Initiatives

pubs.organisational-group

Duke Innovation & Entrepreneurship

pubs.organisational-group

Pediatrics, Transplant and Cellular Therapy

pubs.publication-status

Published

pubs.volume

9

Files

Original bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
p367 Qu.pdf
Size:
1.36 MB
Format:
Adobe Portable Document Format
Description:
Published version