Published January 1, 2019 | Version v1
Journal article Open

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

  • 1. San Raffaele Sci Inst IRCCS, San Raffaele Telethon Inst Gene Therapy SR Tiget, Via Olgettina 58, I-20132 Milan, Italy
  • 2. Jagiellonian Univ, Fac Biochem Biophys & Biotechnol, Krakow, Poland
  • 3. Inst Salud Carlos III, Ctr Nacl Microbiol, Madrid 28220, Spain
  • 4. Katholieke Univ Leuven, Translat Res Gastrointestinal Disorders TARGID, Dept Chron Dis Metab & Ageing, Leuven, Belgium
  • 5. Uludag Univ, Dept Immunol, Fac Med, Bursa, Turkey
  • 6. Czech Acad Sci, Inst Biophys, Brno, Czech Republic
  • 7. Univ Limerick, Dept Biol Sci, Fac Sci & Engn, Limerick, Ireland
  • 8. Univ Munster, Inst Immunol, Munster, Germany
  • 9. Univ Hosp Munster, Mol & Translat Cardiol, Dept Cardiovasc Med, Munster, Germany

Description

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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