Evidence map›Paper›PMID 36380733›Full record

ArticleMolecules and cells2022

Intravenous Mesenchymal Stem Cell Administration Modulates Monocytes/Macrophages and Ameliorates Asthmatic Airway Inflammation in a Murine Asthma Model.

Yosep Mo, Sung-Yoon Kang, Ji-Young Bang, Yujin Kim, Jiung Jeong, Eui-Man Jeong, Hye Young Kim, Sang-Heon Cho, Hye-Ryun Kang

Open access · diamondAbstract read
In one paragraph

Article in Molecules and cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

5 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. 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

9 authors at 3 institutions in 1 country.

Yosep MoInstitute of Allergy and Clinical Immunology, Seoul National University Medical Research Center, Seoul 03080, Korea.ORCID https://orcid.org/0000-0003-0095-4464
Sung-Yoon KangInstitute of Allergy and Clinical Immunology, Seoul National University Medical Research Center, Seoul 03080, Korea.ORCID https://orcid.org/0000-0001-5505-3028
Ji-Young BangInstitute of Allergy and Clinical Immunology, Seoul National University Medical Research Center, Seoul 03080, Korea.ORCID https://orcid.org/0000-0001-6859-4595
Yujin KimInstitute of Allergy and Clinical Immunology, Seoul National University Medical Research Center, Seoul 03080, Korea.ORCID https://orcid.org/0000-0002-9838-5441
Jiung JeongDepartment of Internal Medicine, Seoul National University College of Medicine, Seoul 03080, Korea.ORCID https://orcid.org/0000-0002-4726-7226
Eui-Man JeongDepartment of Pharmacy, Jeju National University College of Pharmacy, Jeju 63243, Korea.ORCID https://orcid.org/0000-0003-0692-2033
Hye Young KimInstitute of Allergy and Clinical Immunology, Seoul National University Medical Research Center, Seoul 03080, Korea.ORCID https://orcid.org/0000-0001-5978-512X
Sang-Heon ChoInstitute of Allergy and Clinical Immunology, Seoul National University Medical Research Center, Seoul 03080, Korea.ORCID https://orcid.org/0000-0002-7644-6469
Hye-Ryun KangInstitute of Allergy and Clinical Immunology, Seoul National University Medical Research Center, Seoul 03080, Korea.ORCID https://orcid.org/0000-0002-2317-4201
Seoul National University · KRJeju National University · KRSeoul National University Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although asthma is a common chronic airway disease that responds well to anti-inflammatory agents, some patients with asthma are unresponsive to conventional treatment. Mesenchymal stem cells (MSCs) have therapeutic potential for the treatment of inflammatory diseases owing to their immunomodulatory properties. However, the target cells of MSCs are not yet clearly known. This study aimed to determine the effect of human umbilical cord-derived MSCs (hUC-MSCs) on asthmatic lungs by modulating innate immune cells and effector T cells using a murine asthmatic model. Intravenously administered hUC-MSCs reduced airway resistance, mucus production, and inflammation in the murine asthma model. hUC-MSCs attenuated not only T helper (Th) 2 cells and Th17 cells but also augmented regulatory T cells (Tregs). As for innate lymphoid cells (ILC), hUC-MSCs effectively suppressed ILC2s by downregulating master regulators of ILC2s, such as

Indexed as

AsthmaMesenchymal Stem CellsMesenchymal Stem Cell TransplantationAnimalsHumansImmunity, InnateInflammationLymphocytesMacrophagesMiceMonocytesUmbilical Cordasthmaimmunityinnatemacrophage activationmesenchymal stem cells

Identifiers

PMID36380733
PMCPMC9676992
OpenAlexW4309320202

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.