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Role of myeloid regulatory cells (MRCs) in maintaining tissue homeostasis and promoting tolerance in autoimmunity, inflammatory disease and transplantation
G. Amodio, J. Cichy, P. Conde, G. Matteoli, A. Moreau, J. Ochando, BH. Oral, M. Pekarova, EJ. Ryan, J. Roth, Y. Sohrabi, MC. Cuturi, S. Gregori,
Jazyk angličtina Země Německo
Typ dokumentu časopisecké články, přehledy
Grantová podpora
BM1404 Mye-EUNITER
COST Action
Project No: 114S354
TUBITAK
(#POR-2013-281)
Irish Health Research Board
2011/02/A/NZ5/00337
Polish National Science Center
LTAUSA17160
Ministry of Education
NLK
PubMed Central
od 1982
Medline Complete (EBSCOhost)
od 2000-04-01
ROAD: Directory of Open Access Scholarly Resources
od 2002
- MeSH
- autoimunita * MeSH
- biologické markery MeSH
- homeostáza * MeSH
- homologní transplantace MeSH
- imunofenotypizace MeSH
- imunologická tolerance * MeSH
- imunomodulace MeSH
- lidé MeSH
- makrofágy imunologie metabolismus MeSH
- monocyty imunologie metabolismus MeSH
- myeloidní buňky imunologie metabolismus MeSH
- náchylnost k nemoci MeSH
- neutrofily imunologie metabolismus MeSH
- T-lymfocyty - podskupiny imunologie metabolismus MeSH
- transplantace orgánů MeSH
- zánět etiologie metabolismus MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
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.
Centro Nacional de Microbiologia Instituto de Salud Carlos 3 Majadahonda 28220 Madrid Spain
Department of Immunology Faculty of Medicine Uludag University Bursa Turkey
Faculty of Biochemistry Biophysics and Biotechnology Jagiellonian University Krakow Poland
Institute of Biophysics The Czech Academy of Sciences Brno Czech Republic
Institute of Immunology University of Münster Münster Germany
Citace poskytuje Crossref.org
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- $a 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.
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