Evidence map›Paper›PMID 34353366›Full record

ArticleStem cell research & therapy2021

IL-1β primed mesenchymal stromal cells moderate hemorrhagic shock-induced organ injuries.

Clotilde Aussel, Nathalie Baudry, Marion Grosbot, Cécile Caron, Eric Vicaut, Sébastien Banzet, Juliette Peltzer

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

13 citing papers in PubMed, 19 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

7 authors at 2 institutions in 1 country.

Clotilde AusselInstitut de Recherche Biomédicale des Armées (IRBA), 1 rue du Lieutenant Raoul Batany, 92141, Clamart, France.
Nathalie BaudryLaboratoire d'Etude de la Microcirculation, UMRS 942 INSERM, University of Paris, Paris, France.
Marion GrosbotInstitut de Recherche Biomédicale des Armées (IRBA), 1 rue du Lieutenant Raoul Batany, 92141, Clamart, France.
Cécile CaronInstitut de Recherche Biomédicale des Armées (IRBA), 1 rue du Lieutenant Raoul Batany, 92141, Clamart, France.
Eric VicautLaboratoire d'Etude de la Microcirculation, UMRS 942 INSERM, University of Paris, Paris, France.
Sébastien BanzetInstitut de Recherche Biomédicale des Armées (IRBA), 1 rue du Lieutenant Raoul Batany, 92141, Clamart, France.
Juliette PeltzerInstitut de Recherche Biomédicale des Armées (IRBA), 1 rue du Lieutenant Raoul Batany, 92141, Clamart, France. juliette.peltzer@inserm.fr.ORCID http://orcid.org/0000-0002-4742-7912
Université Paris-Saclay · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOrgan damages following hemorrhagic shock (HS) have been partly attributed to an immunological dysfunction. The current challenge in the management of HS patients is to prevent organ injury-induced morbidity and mortality which currently has not etiological treatment available. Mesenchymal stromal cells (MSC) are used in clinical cell therapy for immunomodulation and tissue repair. In vitro priming is often used to improve the immunomodulation efficiency of MSC before administration.

objectiveAssess the effect of naive MSC (MSCn) or interleukin (IL)-1β primed (MSCp) treatment in a context of HS-induced organ injury.

methodsRats underwent fixed pressure HS and were treated with allogenic MSCn or MSCp. Liver and kidney injuries were evaluated 6h later by histological and biochemical analysis. Whole blood was collected to measure leukocytes phenotypes. Then, in vitro characterization of MSCn or MSCp was carried out.

resultsPlasma creatinine, blood urea nitrogen, and cystatin C were decrease by MSCp infusion as well as kidney injury molecule (KIM)-1 on histological kidney sections. Transaminases, GGT, and liver histology were normalized by MSCp. Systemic cytokines (IL-1α, IL-6, and IL-10) as well as CD80, 86, and PD-1/PDL-1 axis were decreased by MSCp on monocytes and granulocytes. In vitro, MSCp showed higher level of secreted immunomodulatory molecules than MSCn.

conclusionAn early administration of MSCp moderates HS-induced kidney and liver injury. IL-1β priming improves MSC efficiency by promoting their immunomodulatory activity. These data provide proof of concept that MSCp could be a therapeutic tool to prevent the appearance of organs injury following HS.

Indexed as

Mesenchymal Stem CellsShock, HemorrhagicAnimalsCytokinesHumansImmunomodulationKidneyRatsCytokinesHemorrhagic shockIL-1βImmunomodulationMesenchymal stromal cellsMultiple organ dysfunction syndromePriming

Identifiers

PMID34353366
PMCPMC8340459
OpenAlexW3187119724

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LicenceCC BY
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Registered trials

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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.