Myeloid-derived suppressor cells as cellular immunotherapy in transplantation and autoimmune diseases
•MDSC cell therapy represents a new paradigm in the treatment of immunopathology.•Preclinical success in treatment of transplant rejection, GVHD and autoimmune disease.•Heterogenous results highlight need to tightly control parameters of MDSC therapy. Myeloid-derived suppressor cells (MDSCs) are a h...
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Published in | Cellular immunology Vol. 362; p. 104300 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
Elsevier Inc
01.04.2021
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Subjects | |
Online Access | Get full text |
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Summary: | •MDSC cell therapy represents a new paradigm in the treatment of immunopathology.•Preclinical success in treatment of transplant rejection, GVHD and autoimmune disease.•Heterogenous results highlight need to tightly control parameters of MDSC therapy.
Myeloid-derived suppressor cells (MDSCs) are a heterogeneous population of immature myeloid cells, which have been characterized for their immunosuppressive capacity through multiple mechanisms. These cells have been extensively studied in the field of tumor immunity. Emerging evidence has highlighted its essential role in maintaining immune tolerance in transplantation and autoimmunity. Because of their robust immune inhibitory activities, there has been growing interest in MDSC-based cellular therapy. Various pre-clinical studies have demonstrated that the adoptive transfer of MDCS represented a promising therapeutic strategy for immune-related disorders. In this review, we summarize relevant studies of MDSC-based cell therapy in transplantation and autoimmune diseases and discuss the challenges and future directions for clinical application of MDSC-based cell therapy. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-2 JZ, AH, P-YP and S-HC contributed to the intellectual content of the manuscript and contributed to the drafting of the manuscript. All authors read and approved of the final manuscript. Author Contributions |
ISSN: | 0008-8749 1090-2163 |
DOI: | 10.1016/j.cellimm.2021.104300 |