Evidence map›Paper›PMID 37259141›Full record

ArticleRespiratory research2023

Integrin α10β1-selected mesenchymal stem cells reduced hypercoagulopathy in a porcine model of acute respiratory distress syndrome.

Dag Edström, Anna Niroomand, Martin Stenlo, Kristina Uvebrant, Deniz A Bölükbas, Gabriel Hirdman, Ellen Broberg, Hooi Ching Lim, Snejana Hyllén, Evy Lundgren-Åkerlund and 3 more

Open access · goldAbstract read
In one paragraph

Article in Respiratory research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Time as a Therapeutic Ally: The Promise of Long-Term Solid Organ and Tissue Perfusion.Transplant international : official journal of the European Society for Organ Transplantation · 2026
    Review
  3. Article
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

13 authors at 1 institution in 2 countries.

Dag EdströmDepartment of Cardiothoracic Anaesthesia and Intensive Care, Lund University Hospital, Lund, Sweden.
Anna NiroomandWallenberg Center for Molecular Medicine, Lund University, Lund, Sweden.
Martin StenloDepartment of Cardiothoracic Anaesthesia and Intensive Care, Lund University Hospital, Lund, Sweden.
Kristina UvebrantXintela AB, Lund, Sweden.
Deniz A BölükbasWallenberg Center for Molecular Medicine, Lund University, Lund, Sweden.
Gabriel HirdmanWallenberg Center for Molecular Medicine, Lund University, Lund, Sweden.
Ellen BrobergDepartment of Cardiothoracic Anaesthesia and Intensive Care, Lund University Hospital, Lund, Sweden.
Hooi Ching LimXintela AB, Lund, Sweden.
Snejana HyllénDepartment of Cardiothoracic Anaesthesia and Intensive Care, Lund University Hospital, Lund, Sweden.
Evy Lundgren-ÅkerlundXintela AB, Lund, Sweden.
Leif PierreWallenberg Center for Molecular Medicine, Lund University, Lund, Sweden.
Franziska OlmWallenberg Center for Molecular Medicine, Lund University, Lund, Sweden.
Sandra LindstedtWallenberg Center for Molecular Medicine, Lund University, Lund, Sweden. sandra.lindstedt_ingemansson@med.lu.se.
Lund University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mesenchymal stem cells (MSCs) have been studied for their potential benefits in treating acute respiratory distress syndrome (ARDS) and have reported mild effects when trialed within human clinical trials. MSCs have been investigated in preclinical models with efficacy when administered at the time of lung injury. Human integrin α10β1-selected adipose tissue-derived MSCs (integrin α10β1-MSCs) have shown immunomodulatory and regenerative effects in various disease models. We hypothesized that integrin α10β1 selected-MSCs can be used to treat a sepsis-induced ARDS in a porcine model when administering cells after established injury rather than simultaneously. This was hypothesized to reflect a clinical picture of treatment with MSCs in human ARDS. 12 pigs were randomized to the treated or placebo-controlled group prior to the induction of mild to moderate ARDS via lipopolysaccharide administration. The treated group received 5 × 10

Indexed as

Lung InjuryMesenchymal Stem CellsMesenchymal Stem Cell TransplantationRespiratory Distress SyndromeAnimalsIntegrinsRetrospective StudiesSwineIntegrinsAcute respiratory distress syndromeAdvanced therapeutic medicinal productsIntegrin α10β1 mesenchymal stem cellsLung disease

Identifiers

PMID37259141
PMCPMC10230488
OpenAlexW4378902742

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.