Evidence map›Paper›PMID 34970706›Full record

ReviewIntensive care medicine experimental2021

Mesenchymal stem/stromal cell-based therapies for severe viral pneumonia: therapeutic potential and challenges.

C H Masterson, A Ceccato, A Artigas, C Dos Santos, P R Rocco, S Rolandsson Enes, D J Weiss, D McAuley, M A Matthay, K English and 2 more

Open access · goldAbstract readReview
In one paragraph

Review in Intensive care medicine experimental, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.3field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 11 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 12 institutions in 7 countries.

C H MastersonAnaesthesia, School of Medicine, National University of Ireland, Galway, Ireland.
A CeccatoIntensive Care Unit, Hospital Universitari Sagrat Cor, Barcelona, Spain.
A ArtigasCIBER de Enfermedades Respiratorias (CIBERES), Sabbadell, Spain.
C Dos SantosKeenan Center for Biomedical Research, St. Michael's Hospital, Bond St, Toronto, Canada.
P R RoccoLaboratory of Pulmonary Investigation, Carlos Chagas Filho Institute of Biophysics, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
S Rolandsson EnesDepartment of Experimental Medical Science, Faculty of Medicine, Lund University, Lund, Sweden.
D J WeissDepartment of Medicine, University of Vermont College of Medicine, Burlington, VT, 05405, USA.
D McAuleyRegional Intensive Care Unit, Royal Victoria Hospital, Belfast, UK.
M A MatthayDepartment of Medicine and Anesthesia, University of California, San Francisco, CA, USA.
K EnglishDepartment of Biology, Maynooth University, Maynooth, Co. Kildare, Ireland.
G F CurleyAnaesthesia, School of Medicine, Royal College of Surgeons in Ireland, Dublin 9, Ireland.
J G LaffeyAnaesthesia, School of Medicine, National University of Ireland, Galway, Ireland. john.laffey@nuigalway.ie.ORCID http://orcid.org/0000-0002-1246-9573
Centro de Investigación Biomédica en Red de Enfermedades Respiratorias · ESLund University · SENational University of Ireland · IENational University of Ireland, Maynooth · IEOllscoil na Gaillimhe – University of Galway · IEQueen's University Belfast · GBRoyal College of Surgeons in Ireland · IESt. Michael's Hospital · CAUniversidade Federal do Rio de Janeiro · BRUniversitat Autònoma de Barcelona · ESUniversity of California, San Francisco · USUniversity of Vermont · US

Funding

Medical Research Council MR/M009149/1Science Foundation Ireland 16-FRL-3845
6 · The paper itself

Abstract

Severe viral pneumonia is a significant cause of morbidity and mortality globally, whether due to outbreaks of endemic viruses, periodic viral epidemics, or the rarer but devastating global viral pandemics. While limited anti-viral therapies exist, there is a paucity of direct therapies to directly attenuate viral pneumonia-induced lung injury, and management therefore remains largely supportive. Mesenchymal stromal/stem cells (MSCs) are receiving considerable attention as a cytotherapeutic for viral pneumonia. Several properties of MSCs position them as a promising therapeutic strategy for viral pneumonia-induced lung injury as demonstrated in pre-clinical studies in relevant models. More recently, early phase clinical studies have demonstrated a reassuring safety profile of these cells. These investigations have taken on an added importance and urgency during the COVID-19 pandemic, with multiple trials in progress across the globe. In parallel with clinical translation, strategies are being investigated to enhance the therapeutic potential of these cells in vivo, with different MSC tissue sources, specific cellular products including cell-free options, and strategies to 'licence' or 'pre-activate' these cells, all being explored. This review will assess the therapeutic potential of MSC-based therapies for severe viral pneumonia. It will describe the aetiology and epidemiology of severe viral pneumonia, describe current therapeutic approaches, and examine the data suggesting therapeutic potential of MSCs for severe viral pneumonia in pre-clinical and clinical studies. The challenges and opportunities for MSC-based therapies will then be considered.

Indexed as

Acute hypoxic respiratory failureAcute respiratory distress syndromeCell therapyCoronavirusCritical illnessInfluenzaMesenchymal stem cellsPandemicPneumoniaSepsis

Identifiers

PMID34970706
PMCPMC8718182
OpenAlexW4206367653

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.