Evidence map›Paper›PMID 35402859›Full record

ArticleiScience2022

Poly(I:C) enhances mesenchymal stem cell control of myeloid cells from COVID-19 patients.

Luciana Souza-Moreira, Yuan Tan, Yan Wang, Jia-Pey Wang, Mahmoud Salkhordeh, Jennifer Virgo, Maria Florian, Aidan B P Murray, Irene Watpool, Lauralyn McIntyre and 3 more

Open access · goldAbstract read
In one paragraph

Article in iScience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 19% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. 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 2 institutions in 1 country.

Luciana Souza-MoreiraRegenerative Medicine Program, Ottawa Hospital Research Institute, Ottawa K1H 8L6, ON, Canada.
Yuan TanRegenerative Medicine Program, Ottawa Hospital Research Institute, Ottawa K1H 8L6, ON, Canada.
Yan WangRegenerative Medicine Program, Ottawa Hospital Research Institute, Ottawa K1H 8L6, ON, Canada.
Jia-Pey WangRegenerative Medicine Program, Ottawa Hospital Research Institute, Ottawa K1H 8L6, ON, Canada.
Mahmoud SalkhordehRegenerative Medicine Program, Ottawa Hospital Research Institute, Ottawa K1H 8L6, ON, Canada.
Jennifer VirgoRegenerative Medicine Program, Ottawa Hospital Research Institute, Ottawa K1H 8L6, ON, Canada.
Maria FlorianRegenerative Medicine Program, Ottawa Hospital Research Institute, Ottawa K1H 8L6, ON, Canada.
Aidan B P MurrayRegenerative Medicine Program, Ottawa Hospital Research Institute, Ottawa K1H 8L6, ON, Canada.
Irene WatpoolCritical Care, The Ottawa Hospital, Ottawa, ON K1H 8L6, Canada.
Lauralyn McIntyreFaculty of Medicine, University of Ottawa, Ottawa, ON K1H 8L1, Canada.
Shane EnglishCritical Care, The Ottawa Hospital, Ottawa, ON K1H 8L6, Canada.
Duncan J StewartRegenerative Medicine Program, Ottawa Hospital Research Institute, Ottawa K1H 8L6, ON, Canada.
Shirley H J MeiRegenerative Medicine Program, Ottawa Hospital Research Institute, Ottawa K1H 8L6, ON, Canada.
Ottawa Hospital · CAUniversity of Ottawa · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mesenchymal stem cells (MSCs) are being studied for the treatment of COVID-19-associated critical illness, due to their immunomodulatory properties. Here, we hypothesized that viral mimic-priming improves MSCs' abilities to rebalance the dysregulated immune responses in COVID-19. Transcriptome analysis of poly(I:C)-primed MSCs (pIC-MSCs) showed upregulation of pathways in antiviral and immunomodulatory responses. Together with increased expression of antiviral proteins such as MX1, IFITM3, and OAS1, these changes translated to greater effector functions in regulating monocytes and granulocytes while further enhancing MSCs' ability to block SARS-CoV-2 pseudovirus entry into epithelial cells. Most importantly, the addition of pIC-MSCs to COVID-19 patient whole blood significantly reduced inflammatory neutrophils and increased M2 monocytes while enhancing their phagocytic effector function. We reveal for the first time that MSCs can be primed by Toll-like receptor 3 agonist to improve their ability to rebalance the dysregulated immune responses seen in severe SARS-CoV-2 infection.

Indexed as

ImmunologyStem cells researchVirology

Identifiers

PMID35402859
PMCPMC8975597
OpenAlexW4223618378

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.