How to measure the immunosuppressive activity of MDSC: assays, problems and potential solutions

被引:103
作者
Bruger, Annika M. [1 ]
Dorhoi, Anca [2 ,3 ]
Esendagli, Gunes [4 ]
Barczyk-Kahlert, Katarzyna [5 ]
van der Bruggen, Pierre [1 ]
Lipoldova, Marie [6 ]
Perecko, Tomas [7 ]
Santibanez, Juan [8 ,9 ]
Saraiva, Margarida [10 ,11 ]
Van Ginderachter, Jo A. [12 ,13 ]
Brandau, Sven [14 ]
机构
[1] Catholic Univ Louvain, de Duve Inst, Ave Hippocrate 74, B-1200 Brussels, Belgium
[2] Friedrich Loeffler Inst, Inst Immunol, Fed Res Inst Anim Hlth, Greifswald, Germany
[3] Ernst Moritz Arndt Univ Greifswald, Fac Math & Nat Sci, Greifswald, Germany
[4] Hacettepe Univ, Inst Canc, Dept Basic Oncol, Ankara, Turkey
[5] Univ Munster, Inst Immunol, Munster, Germany
[6] AS CR, Lab Mol & Cellular Immunol, Inst Mol Genet, Videnska 1083, Prague 14220 4, Czech Republic
[7] Slovak Acad Sci, Inst Expt Pharmacol & Toxicol, Dubravska Cesta 9, Bratislava 84104, Slovakia
[8] Univ Belgrade, Mol Oncol Grp, Inst Med Res, Belgrade, Serbia
[9] Univ Bernardo OHiggins, CIBQA, Santiago, Chile
[10] Univ Porto, Inst Invest & Inovacao Saude, Porto, Portugal
[11] Univ Porto, Inst Biol Mol & Celular, Porto, Portugal
[12] Vrije Univ Brussel, Cellular & Mol Immunol Lab, Brussels, Belgium
[13] VIB Ctr Inflammat Res, Myeloid Cell Immunol Lab, Brussels, Belgium
[14] Univ Hosp Essen, Div Res, Dept Otorhinolaryngol, West German Canc Ctr, Hufelandstr 55, D-45122 Essen, Germany
关键词
Myeloid-derived suppressor cells; T cells; Immunosuppression; Arginase; Proliferation; Mye-EUNITER; MYELOID SUPPRESSOR-CELLS; T REGULATORY CELLS; PERIPHERAL-BLOOD; DENDRITIC CELLS; ARGINASE-I; CANCER; INHIBITION; DIFFERENTIATION; NEUTROPHILS; POPULATION;
D O I
10.1007/s00262-018-2170-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:631 / 644
页数:14
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