New Perspectives on Myeloid-Derived Suppressor Cells and Their Emerging Role in Haematology

被引:9
作者
Bizymi, Nikoleta [1 ,2 ,3 ]
Matthaiou, Andreas M. [3 ,4 ]
Matheakakis, Angelos [1 ,2 ]
Voulgari, Ioanna [1 ,2 ]
Aresti, Nikoletta [1 ,2 ]
Zavitsanou, Konstantina [1 ,2 ]
Karasachinidis, Anastasios [1 ,2 ]
Mavroudi, Irene [1 ,2 ]
Pontikoglou, Charalampos [1 ,2 ]
Papadaki, Helen A. [1 ,2 ]
机构
[1] Univ Hosp Heraklion, Dept Haematol, Iraklion 71500, Crete, Greece
[2] Univ Crete, Sch Med, Haemopoiesis Res Lab, Iraklion 71003, Crete, Greece
[3] Univ Crete, Sch Med, Lab Mol & Cellular Pneumonol, Iraklion 71003, Crete, Greece
[4] Univ Cyprus, Med Sch, Resp Physiol Lab, CY-2029 Nicosia, Cyprus
关键词
myeloid-derived suppressor cell (MDSC); haematology; immunology; cancer; infection; autoimmunity; inflammation; immunotherapy; immune dysregulation; biomarker; CORD BLOOD; T-CELLS; IMMUNOSUPPRESSIVE ACTIVITY; PROMOTE ANGIOGENESIS; HEMATOPOIETIC STEM; CANCER; MDSCS; EXPRESSION; EXPANSION; DIFFERENTIATION;
D O I
10.3390/jcm11185326
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Myeloid-derived suppressor cells (MDSCs) are immature cells of myeloid origin that have gained researchers' attention, as they constitute promising biomarkers and targets for novel therapeutic strategies (i.e., blockage of development, differentiation, depletion, and deactivation) in several conditions, including neoplastic, autoimmune, infective, and inflammatory diseases, as well as pregnancy, obesity, and graft rejection. They are characterised in humans by the typical immunophenotype of CD11b(+)CD33(+)HLA-DR-/low and immune-modulating properties leading to decreased T-cell proliferation, induction of T-regulatory cells (T-regs), hindering of natural killer (NK) cell functionality, and macrophage M2-polarisation. The research in the field is challenging, as there are still difficulties in defining cell-surface markers and gating strategies that uniquely identify the different populations of MDSCs, and the currently available functional assays are highly demanding. There is evidence that MDSCs display altered frequency and/or functionality and could be targeted in immune-mediated and malignant haematologic diseases, although there is a large variability of techniques and results between different laboratories. This review presents the current literature concerning MDSCs in a clinical point of view in an attempt to trigger future investigation by serving as a guide to the clinical haematologist in order to apply them in the context of precision medicine as well as the researcher in the field of experimental haematology.
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页数:23
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共 173 条
[1]   Expansion of myeloid-derived suppressor cells in patients with severe coronavirus disease (COVID-19) [J].
Agrati, Chiara ;
Sacchi, Alessandra ;
Bordoni, Veronica ;
Cimini, Eleonora ;
Notari, Stefania ;
Grassi, Germana ;
Casetti, Rita ;
Tartaglia, Eleonora ;
Lalle, Eleonora ;
D'Abramo, Alessandra ;
Castilletti, Concetta ;
Marchioni, Luisa ;
Shi, Yufang ;
Mariano, Andrea ;
Song, Jin-Wen ;
Zhang, Ji-Yuan ;
Wang, Fu-Sheng ;
Zhang, Chao ;
Fimia, Gian Maria ;
Capobianchi, Maria R. ;
Piacentini, Mauro ;
Antinori, Andrea ;
Nicastri, Emanuele ;
Maeurer, Markus ;
Zumla, Alimuddin ;
Ippolito, Giuseppe .
CELL DEATH AND DIFFERENTIATION, 2020, 27 (11) :3196-3207
[2]   The Emerging Role of CD244 Signaling in Immune Cells of the Tumor Microenvironment [J].
Agresta, Laura ;
Hoebe, Kasper H. N. ;
Janssen, Edith M. .
FRONTIERS IN IMMUNOLOGY, 2018, 9
[3]   MDSCs in pregnancy: Critical players for a balanced immune system at the feto-maternal interface [J].
Ahmadi, Moslem ;
Mohammadi, Mobin ;
Ali-Hassanzadeh, Mohammad ;
Zare, Maryam ;
Gharesi-Fard, Behrouz .
CELLULAR IMMUNOLOGY, 2019, 346
[4]   Energy metabolic pathways control the fate and function of myeloid immune cells [J].
Al-Khami, Amir A. ;
Rodriguez, Paulo C. ;
Ochoa, Augusto C. .
JOURNAL OF LEUKOCYTE BIOLOGY, 2017, 102 (02) :369-380
[5]   Autophagy orchestrates the regulatory program of tumor-associated myeloid-derived suppressor cells [J].
Alissafi, Themis ;
Hatzioannou, Aikaterini ;
Mintzas, Konstantinos ;
Barouni, Roza Maria ;
Banos, Aggelos ;
Sormendi, Sundary ;
Polyzos, Alexandros ;
Xilouri, Maria ;
Wielockx, Ben ;
Gogas, Helen ;
Verginis, Panayotis .
JOURNAL OF CLINICAL INVESTIGATION, 2018, 128 (09) :3840-3852
[6]   Recent insights into the function of autophagy in cancer [J].
Amaravadi, Ravi ;
Kimmelman, Alec C. ;
White, Eileen .
GENES & DEVELOPMENT, 2016, 30 (17) :1913-1930
[7]   Characterization of a whole blood assay for quantifying myeloid-derived suppressor cells [J].
Apodaca, Minjun C. ;
Wright, Amy E. ;
Riggins, Angela M. ;
Harris, William P. ;
Yeung, Raymond S. ;
Yu, Lei ;
Morishima, Chihiro .
JOURNAL FOR IMMUNOTHERAPY OF CANCER, 2019, 7 (01)
[8]   Enhancing T cell therapy by overcoming the immunosuppressive tumor microenvironment [J].
Arina, Ainhoa ;
Corrales, Leticia ;
Bronte, Vincenzo .
SEMINARS IN IMMUNOLOGY, 2016, 28 (01) :54-63
[9]   Intravenous immunoglobulin treatment of spleen cells from patients with immune thrombocytopenia significantly increases the percentage of myeloid-derived suppressor cells [J].
Aslam, Rukhsana ;
Burack, W. Richard ;
Segel, George B. ;
McVey, Mark ;
Spence, Stephen A. ;
Semple, John W. .
BRITISH JOURNAL OF HAEMATOLOGY, 2018, 181 (02) :262-264
[10]   STAT proteins: a kaleidoscope of canonical and non-canonical functions in immunity and cancer [J].
Awasthi, Nagendra ;
Liongue, Clifford ;
Ward, Alister C. .
JOURNAL OF HEMATOLOGY & ONCOLOGY, 2021, 14 (01)