Evidence map›Paper›PMID 30357490›Full record

ReviewCancer immunology, immunotherapy : CII2019

Role of myeloid regulatory cells (MRCs) in maintaining tissue homeostasis and promoting tolerance in autoimmunity, inflammatory disease and transplantation.

Giada Amodio, Joanna Cichy, Patricia Conde, Gianluca Matteoli, Aurélie Moreau, Jordi Ochando, Barbaros H Oral, Michaela Pekarova, Elizabeth J Ryan, Johannes Roth and 3 more

Open access · hybridAbstract readReview
In one paragraph

Review in Cancer immunology, immunotherapy : CII, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

44 citing papers in PubMed, 65 citations in OpenAlex.

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  10. Shifting phenotype and differentiation of CD11bInflammation research : official journal of the European Histamine Research Society ... [et al.] · 2024
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  20. Clinical perspectives on the age-related increase of immunosuppressive activity.Journal of molecular medicine (Berlin, Germany) · 2022
    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

13 authors at 10 institutions in 9 countries.

Giada AmodioSan Raffaele Telethon Institute for Gene Therapy (SR-Tiget), San Raffaele Scientific Institute IRCCS, Via Olgettina, 58, 20132, Milan, Italy.ORCID http://orcid.org/0000-0002-2457-387X
Joanna CichyFaculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, Krakow, Poland.ORCID http://orcid.org/0000-0002-0552-8344
Patricia CondeCentro Nacional de Microbiologia, Instituto de Salud Carlos III, Majadahonda, 28220, , Madrid, Spain.ORCID http://orcid.org/0000-0003-2022-5568
Gianluca MatteoliTranslational Research in Gastrointestinal Disorders (TARGID), Department of Chronic Diseases, Metabolism and Ageing, KU Leuven, Leuven, Belgium.ORCID http://orcid.org/0000-0002-2902-4976
Aurélie MoreauCentre de Recherche en Transplantation et Immunologie UMR1064, INSERM, Université de Nantes, Nantes, France.ORCID http://orcid.org/0000-0002-8519-2632
Jordi OchandoCentro Nacional de Microbiologia, Instituto de Salud Carlos III, Majadahonda, 28220, , Madrid, Spain.ORCID http://orcid.org/0000-0001-7037-1681
Barbaros H OralDepartment of Immunology, Faculty of Medicine, Uludag University, Bursa, Turkey.ORCID http://orcid.org/0000-0003-0463-6818
Michaela PekarovaInstitute of Biophysics, The Czech Academy of Sciences, Brno, Czech Republic.ORCID http://orcid.org/0000-0003-1252-455X
Elizabeth J RyanDepartment of Biological Sciences, Faculty of Science and Engineering, University of Limerick, Limerick, Ireland.ORCID http://orcid.org/0000-0002-5137-1253
Johannes RothInstitute of Immunology, University of Münster, Münster, Germany.
Yahya SohrabiMolecular and Translational Cardiology, Department of Cardiovascular Medicine, University Hospital Münster, Münster, Germany.ORCID http://orcid.org/0000-0001-5268-238X
Maria-Cristina CuturiCentre de Recherche en Transplantation et Immunologie UMR1064, INSERM, Université de Nantes, Nantes, France.ORCID http://orcid.org/0000-0001-5249-7467
Silvia GregoriSan Raffaele Telethon Institute for Gene Therapy (SR-Tiget), San Raffaele Scientific Institute IRCCS, Via Olgettina, 58, 20132, Milan, Italy. gregori.silvia@hsr.it.ORCID http://orcid.org/0000-0002-3517-9683
Inserm · FRInstituto de Salud Carlos III · ESThe San Raffaele Telethon Institute for Gene Therapy · ITBursa Uludağ Üni̇versi̇tesi̇ · TRCzech Academy of Sciences, Institute of Biophysics · CZJagiellonian University · PLKU Leuven · BEUniversity Hospital Münster · DEUniversity of Limerick · IEUniversity of Münster · DE

Funding

COST Action BM1404 Mye-EUNITERIrish Health Research Board (#POR-2013-281)Ministry of Education LTAUSA17160Polish National Science Center 2011/02/A/NZ5/00337TUBITAK Project No: 114S354
6 · The paper itself

Abstract

Myeloid cells play a pivotal role in regulating innate and adaptive immune responses. In inflammation, autoimmunity, and after transplantation, myeloid cells have contrasting roles: on the one hand they initiate the immune response, promoting activation and expansion of effector T-cells, and on the other, they counter-regulate inflammation, maintain tissue homeostasis, and promote tolerance. The latter activities are mediated by several myeloid cells including polymorphonuclear neutrophils, macrophages, myeloid-derived suppressor cells, and dendritic cells. Since these cells have been associated with immune suppression and tolerance, they will be further referred to as myeloid regulatory cells (MRCs). In recent years, MRCs have emerged as a therapeutic target or have been regarded as a potential cellular therapeutic product for tolerance induction. However, several open questions must be addressed to enable the therapeutic application of MRCs including: how do they function at the site of inflammation, how to best target these cells to modulate their activities, and how to isolate or to generate pure populations for adoptive cell therapies. In this review, we will give an overview of the current knowledge on MRCs in inflammation, autoimmunity, and transplantation. We will discuss current strategies to target MRCs and to exploit their tolerogenic potential as a cell-based therapy.

Indexed as

AutoimmunityHomeostasisImmune ToleranceAnimalsBiomarkersDisease SusceptibilityHumansImmunomodulationImmunophenotypingInflammationMacrophagesMonocytesMyeloid CellsNeutrophilsOrgan TransplantationT-Lymphocyte SubsetsBiomarkersDendritic cellsMonocytes/macrophagesMye-EUNITERMyeloid regulatory cells (MRCs)Polymorphonuclear neutrophilsTolerance

Identifiers

PMID30357490
PMCPMC6447499
OpenAlexW2898591181

What OpenQuestion holds

Textmetadata
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.