Evidence map›Paper›PMID 38031182›Full record

ArticleStem cell research & therapy2023

The effect of TLR3 priming conditions on MSC immunosuppressive properties.

Tatiana Tolstova, Ekaterina Dotsenko, Peter Kozhin, Svetlana Novikova, Victor Zgoda, Alexander Rusanov, Nataliya Luzgina

Abstract read
In one paragraph

Article in Stem cell research & therapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

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  20. Tryptophan catabolism via the kynurenine pathway regulates infection and inflammation: from mechanisms to biomarkers and therapies.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2024
    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

7 authors.

Tatiana TolstovaInstitute of Biomedical Chemistry, Pogodinskaya, Moscow, Russia, 119121.
Ekaterina DotsenkoInstitute of Biomedical Chemistry, Pogodinskaya, Moscow, Russia, 119121.
Peter KozhinInstitute of Biomedical Chemistry, Pogodinskaya, Moscow, Russia, 119121.
Svetlana NovikovaInstitute of Biomedical Chemistry, Pogodinskaya, Moscow, Russia, 119121.
Victor ZgodaInstitute of Biomedical Chemistry, Pogodinskaya, Moscow, Russia, 119121.
Alexander RusanovInstitute of Biomedical Chemistry, Pogodinskaya, Moscow, Russia, 119121. alexander.l.rusanov@gmail.com.
Nataliya LuzginaInstitute of Biomedical Chemistry, Pogodinskaya, Moscow, Russia, 119121.

Funding

Program for Basic Research in the Russian Federation for a long-term period (2021-2030) 122022800481-0
6 · The paper itself

Abstract

backgroundMesenchymal stromal cells (MSCs) have regenerative and immunomodulatory properties, making them suitable for cell therapy. Toll-like receptors (TLRs) in MSCs respond to viral load by secreting immunosuppressive or proinflammatory molecules. The expression of anti-inflammatory molecules in MSCs can be altered by the concentration and duration of exposure to the TLR3 ligand polyinosinic-polycytidylic acid (poly(I:C)). This study aimed to optimize the preconditioning of MSCs with poly(I:C) to increase immunosuppressive effects and to identify MSCs with activated TLR3 (prMSCs).

methodsFlow cytometry and histochemical staining were used to analyze MSCs for immunophenotype and differentiation potential. MSCs were exposed to poly(I:C) at 1 and 10 μg/mL for 1, 3, and 24 h, followed by determination of the expression of IDO1, WARS1, PD-L1, TSG-6, and PTGES2 and PGE2 secretion. MSCs and prMSCs were cocultured with intact (J

resultsPoly(I:C) at 10 μg/mL during a 3-h incubation caused the highest expression of immunosuppression markers in MSCs. Activation of prMSCs caused a 18% decrease in proliferation and a one-third increase in apoptotic J

conclusionsTLR3 activation in MSCs is dependent on exposure time and poly(I:C) concentration. The maximum expression of immunosuppressive molecules was observed with 10 µg/mL poly(I:C) for 3-h preconditioning. This priming protocol for MSCs enhances the immunosuppressive effects of prMSCs on T cells.

Indexed as

Interleukin-10Toll-Like Receptor 3Anti-Inflammatory AgentsAntiviral AgentsHumansImmunosuppressive AgentsInterleukin-2ProteomicsUbiquitin ThiolesteraseAnti-Inflammatory AgentsAntiviral AgentsImmunosuppressive AgentsInterleukin-10Interleukin-2TLR3 protein, humanToll-Like Receptor 3Ubiquitin ThiolesteraseUSP18 protein, humanImmunosuppressionJurkatMSCsPoly(I:C)TLR3Toll-like receptors

Identifiers

PMID38031182
PMCPMC10687850

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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.