How to measure the immunosuppressive activity of MDSC: assays, problems and potential solutions
Language English Country Germany Media print-electronic
Document type Journal Article, Review
Grant support
BM1404
European Cooperation in Science and Technology
PubMed
29785656
PubMed Central
PMC11028070
DOI
10.1007/s00262-018-2170-8
PII: 10.1007/s00262-018-2170-8
Knihovny.cz E-resources
- Keywords
- Arginase, Immunosuppression, Mye-EUNITER, Myeloid-derived suppressor cells, Proliferation, T cells,
- MeSH
- Lymphocyte Activation immunology MeSH
- Biomarkers MeSH
- Cytokines metabolism MeSH
- Phenotype MeSH
- Immunophenotyping MeSH
- Immunomodulation MeSH
- Humans MeSH
- Cell Communication immunology MeSH
- Myeloid-Derived Suppressor Cells immunology metabolism MeSH
- T-Lymphocytes immunology metabolism MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Review MeSH
- Names of Substances
- Biomarkers MeSH
- Cytokines MeSH
Myeloid-derived suppressor cells (MDSC) are a heterogeneous group of mononuclear and polymorphonuclear myeloid cells, which are present at very low numbers in healthy subjects, but can expand substantially under disease conditions. Depending on disease type and stage, MDSC comprise varying amounts of immature and mature differentiation stages of myeloid cells. Validated unique phenotypic markers for MDSC are still lacking. Therefore, the functional analysis of these cells is of central importance for their identification and characterization. Various disease-promoting and immunosuppressive functions of MDSC are reported in the literature. Among those, the capacity to modulate the activity of T cells is by far the most often used and best-established read-out system. In this review, we critically evaluate the assays available for the functional analysis of human and murine MDSC under in vitro and in vivo conditions. We also discuss critical issues and controls associated with those assays. We aim at providing suggestions and recommendations useful for the contemporary biological characterization of MDSC.
Cellular and Molecular Immunology Lab Vrije Universiteit Brussel Brussels Belgium
Centro Integrativo de Biología y Química Aplicada Universidad Bernardo O'Higgins Santiago Chile
Department of Basic Oncology Hacettepe University Cancer Institute Ankara Turkey
e Duve Institute Université catholique de Louvain Avenue Hippocrate 74 1200 Brussels Belgium
Institute of Immunology University of Münster Münster Germany
Instituto de Biologia Molecular e Celular University of Porto Porto Portugal
Instituto de Investigação e Inovação em Saúde University of Porto Porto Portugal
Myeloid Cell Immunology Lab VIB Center for Inflammation Research Brussels Belgium
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