Evidence map›Paper›PMID 33899029›Full record

ArticleJTCVS open2021

Influence of administration of mesenchymal stromal cell on pediatric oxygenator performance and inflammatory response.

Takuya Maeda, Casey M Briggs, Anushree Datar, Christine A Brantner, Patrick J Hanley, Richard A Jonas, Nobuyuki Ishibashi

Open access · goldAbstract read
In one paragraph

Article in JTCVS open, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-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

6 citing papers in PubMed, 8 citations in OpenAlex.

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  4. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Takuya MaedaCenter for Neuroscience Research, and Sheikh Zayed Institute for Pediatric Surgical Innovation, Children's National Heart Institute, Washington, DC.
Casey M BriggsCenter for Neuroscience Research, and Sheikh Zayed Institute for Pediatric Surgical Innovation, Children's National Heart Institute, Washington, DC.
Anushree DatarProgram for Cell Enhancement and Technologies for Immunotherapy, Division of Blood and Marrow Transplantation, Center for Cancer and Immunology Research, Children's National Hospital, Washington, DC.
Christine A BrantnerGW Nanofabrication and Imaging Center, The George Washington University School of Medicine and Health Science, Washington, DC.
Patrick J HanleyProgram for Cell Enhancement and Technologies for Immunotherapy, Division of Blood and Marrow Transplantation, Center for Cancer and Immunology Research, Children's National Hospital, Washington, DC.
Richard A JonasCenter for Neuroscience Research, and Sheikh Zayed Institute for Pediatric Surgical Innovation, Children's National Heart Institute, Washington, DC.
Nobuyuki IshibashiCenter for Neuroscience Research, and Sheikh Zayed Institute for Pediatric Surgical Innovation, Children's National Heart Institute, Washington, DC.
George Washington University · USVirginia Commonwealth University · US

Funding

Neurobehavioral Evaluation CoreP50HD105328 · NICHD · CHILDREN'S RESEARCH INSTITUTE · PI WILLIAM Davis GAILLARD · 2021 to 2026
$9.3M
Research_ProjectU54HD090257 · NICHD · CHILDREN'S RESEARCH INSTITUTE · PI LIMPEROPOULOS, CATHERINE · 2016 to 2020
$5.9M
Cell Therapy for Neuroprotection in Congenital Heart DiseaseR01HL139712 · NHLBI · CHILDREN'S RESEARCH INSTITUTE · PI Nobuyuki Ishibashi · 2018 to 2026
$5.7M
White Matter Protection in the Fetus with Congenital Heart DiseaseR01HL146670 · NHLBI · CHILDREN'S RESEARCH INSTITUTE · PI ISHIBASHI, NOBUYUKI · 2020 to 2023
$3.3M
Mesenchymal Stromal Cell Delivery through Cardiopulmonary Bypass in Pediatric Cardiac SurgeryR33HL146394 · NHLBI · CHILDREN'S RESEARCH INSTITUTE · PI BOLLARD, CATHERINE M., ISHIBASHI, NOBUYUKI · 2019 to 2021
$2.6M
NHLBI NIH HHS R01 HL139712NHLBI NIH HHS R01 HL146670NHLBI NIH HHS R33 HL146394NICHD NIH HHS P50 HD105328NICHD NIH HHS U54 HD090257
6 · The paper itself

Abstract

objectiveMesenchymal stromal cells have important immunomodulatory and neuroprotective properties. The aim of this study was to evaluate the feasibility of mesenchymal stromal cell administration into a cardiopulmonary bypass (CPB) circuit, including a pediatric oxygenator, and to assess the immunomodulatory response of the circulating blood prime.

methodsA bypass circuit with a pediatric oxygenator, including integral filter was primed with bank whole blood. Normal saline (control) or 120 × 10

resultsThere were no differences in flow rate, trans-oxygenator pressure gradient, blood oxygen, and carbon dioxide levels between control and cell delivery groups. No adhesion of mesenchymal stromal cells was observed on the filter mesh by scanning electron microscopy. Lymphocyte surface marker assay found no difference in the number of B cells, T cells, or natural killer cells between the 2 groups, indicating no immunogenicity of allogeneic mesenchymal stromal cells under ex vivo CPB conditions. CPB significantly changed the level of interleukin (IL) 4, IL-6, IL-8, IP-10, macrophage colony stimulating factor, macrophage inflammatory protein-1

conclusionsThe administration of mesenchymal stromal cells does not interfere with oxygenator function. Allogeneic mesenchymal stromal cells show no immunogenicity, and increase plasma IL-6 level during ex vivo circulation. Further investigation is necessary to determine the effect of mesenchymal stromal cell delivery through CPB during pediatric cardiac surgery.

Indexed as

cardiopulmonary bypasscell transplantationcerebral protectioncongenital heart diseasemesenchymal stromal cells

Identifiers

PMID33899029
PMCPMC8064572
OpenAlexW3131767175

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.