Evidence map›Paper›PMID 28982177›Full record

ArticlePloS one2017

Adipose-derived stem cells attenuate pulmonary microvascular hyperpermeability after smoke inhalation.

Koji Ihara, Satoshi Fukuda, Baigalmaa Enkhtaivan, Raul Trujillo, Dannelys Perez-Bello, Christina Nelson, Anita Randolph, Suzan Alharbi, Hira Hanif, David Herndon and 2 more

Abstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
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

14 citing papers in PubMed.

  1. Article
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  11. Emerging therapies for smoke inhalation injury: a review.Journal of translational medicine · 2020
    Review
  12. Article
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  14. Review
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.

Koji IharaDepartment of Anesthesiology, The University of Texas Medical Branch, Galveston, Texas, United States of America.ORCID http://orcid.org/0000-0001-5408-8114
Satoshi FukudaDepartment of Anesthesiology, The University of Texas Medical Branch, Galveston, Texas, United States of America.
Baigalmaa EnkhtaivanDepartment of Anesthesiology, The University of Texas Medical Branch, Galveston, Texas, United States of America.
Raul TrujilloDepartment of Anesthesiology, The University of Texas Medical Branch, Galveston, Texas, United States of America.
Dannelys Perez-BelloDepartment of Anesthesiology, The University of Texas Medical Branch, Galveston, Texas, United States of America.
Christina NelsonDepartment of Anesthesiology, The University of Texas Medical Branch, Galveston, Texas, United States of America.
Anita RandolphDepartment of Anesthesiology, The University of Texas Medical Branch, Galveston, Texas, United States of America.
Suzan AlharbiDepartment of Anesthesiology, The University of Texas Medical Branch, Galveston, Texas, United States of America.
Hira HanifDepartment of Anesthesiology, The University of Texas Medical Branch, Galveston, Texas, United States of America.
David HerndonDepartment of Surgery, Shriners Hospital for Children, Galveston, Texas, United States of America.
Donald ProughDepartment of Anesthesiology, The University of Texas Medical Branch, Galveston, Texas, United States of America.
Perenlei EnkhbaatarDepartment of Anesthesiology, The University of Texas Medical Branch, Galveston, Texas, United States of America.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPulmonary edema is a hallmark of acute respiratory distress syndrome (ARDS). Smoke inhalation causes ARDS, thus significantly increasing the mortality of burn patients. Adipose-derived stem cells (ASCs) exert potent anti-inflammatory properties. The goal of the present study was to test the safety and ecfficacy of ASCs, in a well-characterized clinically relevant ovine model of ARDS.

methodsFemale sheep were surgically prepared. ARDS was induced by cooled cotton smoke inhalation. Following injury, sheep were ventilated, resuscitated with lactated Ringer's solution, and cardiopulmonary hemodynamics were monitored for 48 hours in a conscious state. Pulmonary microvascular hyper-permeability was assessed by measuring lung lymph flow, extravascular lung water content, protein content in plasma and lung lymph fluid. Sheep were randomly allocated to two groups: 1) ASCs: infused with 200 million of ASCs in 200mL of PlasmaLyteA starting 1 hours post-injury, n = 5; 2) control, treated with 200mL of PlasmaLyteA in a similar pattern, n = 5.

resultsLung lymph flow increased 9-fold in control sheep as compared to baseline. Protein in the plasma was significantly decreased, while it was increased in the lung lymph. The treatment with ASCs significantly attenuated these changes. Treatment with ASCs almost led to the reversal of increased pulmonary vascular permeability and lung water content. Pulmonary gas exchange was significantly improved by ASCs. Infusion of the ASCs did not negatively affect pulmonary artery pressure and other hemodynamic variables.

conclusionsASCs infusion was well tolerated. The results suggest that intravenous ASCs modulate pulmonary microvascular hyper-permeability and prevent the onset of ARDS in our experimental model.

Indexed as

Capillary PermeabilitySmokeAdipose TissueAnimalsCells, CulturedFemaleHemodynamicsInhalation ExposureLungMicrovesselsSheepStem CellsSmoke

Identifiers

PMID28982177
PMCPMC5628899

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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.