Evidence map›Paper›PMID 32546175›Full record

ArticleCell communication and signaling : CCS2020

The TNF/TNFR2 signaling pathway is a key regulatory factor in endothelial progenitor cell immunosuppressive effect.

Sina Naserian, Mohamed Essameldin Abdelgawad, Mazdak Afshar Bakshloo, Guillaume Ha, Nassim Arouche, José L Cohen, Benoît L Salomon, Georges Uzan

Open access · goldAbstract readVideo-Audio Media
In one paragraph

Article in Cell communication and signaling : CCS, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed
6.5field-weighted citation impact, top 2% 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

75 citing papers in PubMed, 110 citations in OpenAlex.

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  17. Infection and drug resistance · 2025
    Article
  18. Understanding the role of TNFR2 signaling in the tumor microenvironment of breast cancer.Journal of experimental & clinical cancer research : CR · 2024
    Review
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  20. Review

15 more citing papers are in PubMed but not listed here.

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

8 authors at 2 institutions in 2 countries.

Sina NaserianINSERM UMR-S-MD 1197, Hôpital Paul Brousse, Villejuif, France. sina.naserian@inserm.fr.ORCID 0000-0003-3604-8375
Mohamed Essameldin AbdelgawadINSERM UMR-S-MD 1197, Hôpital Paul Brousse, Villejuif, France.
Mazdak Afshar BakshlooINSERM UMR-S-MD 1197, Hôpital Paul Brousse, Villejuif, France.
Guillaume HaINSERM UMR-S-MD 1197, Hôpital Paul Brousse, Villejuif, France.
Nassim AroucheINSERM UMR-S-MD 1197, Hôpital Paul Brousse, Villejuif, France.
José L CohenUniv Paris Est Creteil, INSERM, IMRB, F-94010, Creteil, France.
Benoît L SalomonSorbonne Université, INSERM, CNRS, Centre d'Immunologie et des Maladies Infectieuses (CIMI-Paris), Paris, France.
Georges UzanINSERM UMR-S-MD 1197, Hôpital Paul Brousse, Villejuif, France. georges.uzan@inserm.fr.
Inserm · FRCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEndothelial progenitor cells (EPCs) are non-differentiated endothelial cells (ECs) present in blood circulation that are involved in neo-vascularization and correction of damaged endothelial sites. Since EPCs from patients with vascular disorders are impaired and inefficient, allogenic sources from adult or cord blood are considered as good alternatives. However, due to the reaction of immune system against allogenic cells which usually lead to their elimination, we focused on the exact role of EPCs on immune cells, particularly, T cells which are the most important cells applied in immune rejection. TNFα is one of the main activators of EPCs that recognizes two distinct receptors. TNFR1 is expressed ubiquitously and its interaction with TNFα leads to differentiation and apoptosis, whereas, TNFR2 is expressed predominantly on ECs, immune cells and neural cells and is involved in cell survival and proliferation. Interestingly, it has been shown that different immunosuppressive cells express TNFR2 and this is directly related to their immunosuppressive efficiency. However, little is known about immunological profile and function of TNFR2 in EPCs.

methodsUsing different in-vitro combinations, we performed co-cultures of ECs and T cells to investigate the immunological effect of EPCs on T cells. We interrupted in the TNFα/TNFR2 axis either by blocking the receptor using TNFR2 antagonist or blocking the ligand using T cells derived from TNFα KO mice.

resultsWe demonstrated that EPCs are able to suppress T cell proliferation and modulate them towards less pro-inflammatory and active phenotypes. Moreover, we showed that TNFα/TNFR2 immune-checkpoint pathway is critical in EPC immunomodulatory effect.

conclusionsOur results reveal for the first time a mechanism that EPCs use to suppress immune cells, therefore, enabling them to form new immunosuppressive vessels. Furthermore, we have shown the importance of TNFα/TNFR2 axis in EPCs as an immune checkpoint pathway. We believe that targeting TNFR2 is especially crucial in cancer immune therapy since it controls two crucial aspects of tumor microenvironment: 1) Immunosuppression and 2) Angiogenesis. Video Abstract. (MP4 46355 kb).

Indexed as

Endothelial Progenitor CellsImmunosuppression TherapyAdolescentAdultAgedAnimalsCells, CulturedCoculture TechniquesFemaleHealthy VolunteersHumansMaleMiceMice, Inbred C57BLMiddle AgedReceptors, Tumor Necrosis Factor, Type IIReceptors, Tumor Necrosis Factor, Type IITNF protein, humanTumor Necrosis Factor-alphaCancer immune therapyEndothelial Colony Forming Cells (ECFCs)Endothelial Progenitor Cells (EPCs)Immune-checkpointImmune regulationT cellsTNFα/TNFR2 signaling pathway

Identifiers

PMID32546175
PMCPMC7298859
OpenAlexW3034635593

What OpenQuestion holds

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LicenceCC BY
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.