Myeloid-derived suppressor cells - their role in haemato-oncological malignancies and other cancers and possible implications for therapy

被引:45
作者
Tadmor, Tamar [1 ]
Attias, Dina [1 ]
Polliack, Aaron [2 ,3 ]
机构
[1] Bnai Zion Med Ctr, Haematol Unit, IL-31048 Haifa, Israel
[2] Hadassah Univ Hosp, Dept Haematol, IL-91120 Jerusalem, Israel
[3] Hebrew Univ Jerusalem, Sch Med, IL-91010 Jerusalem, Israel
关键词
myeloid-derived suppressor cells; granulocytic MDSCs; monocytic MDSCs; HEPATOCELLULAR-CARCINOMA; TUMOR MICROENVIRONMENT; IMMUNE DYSFUNCTION; DENDRITIC CELLS; ACCUMULATION; INFLAMMATION; INHIBITION; EXPRESSION; TOLERANCE; MECHANISM;
D O I
10.1111/j.1365-2141.2011.08678.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
P>Myeloid-derived suppressor cells (MDSCs) are a heterogeneous population of immature myeloid cells at different stages of maturation that play a role in cancer tolerance and function as an immune-suppressive cell subpopulation. They utilize different mechanisms to block both innate and adaptive arms of anti-tumour immunity, mostly through inhibition of T cell activation and expansion. Further advances in our understanding of this cell population in both murine models and humans has enabled more accurate characterization of their phenotype and the recognition of two major classes of MDSCs: granulocytic and monocytic. Recently, the mechanism of action and clinical importance of MDSCs has been more clearly defined and their interactions with cancer cells have been shown to be among the factors influencing tumour development and induction of tolerance. Most of the earlier studies were performed using murine models, but recent clinical investigations have shown their potential role in human cancers. Here, we review the origin of MDSCs, their mechanisms of action, the factors influencing their production and related signalling pathways. We focus on their role in human solid tumours and haemato-oncological malignancies, and relate to possible novel therapeutic approaches targeting MDSCs which could be considered together with other anticancer strategies in the not too distant future.
引用
收藏
页码:557 / 567
页数:11
相关论文
共 69 条
[1]   Myeloid-derived suppressor cells in mammary tumor progression in FVB Neu transgenic mice [J].
Abe, Fuminori ;
Dafferner, Alicia J. ;
Donkor, Moses ;
Westphal, Sherry N. ;
Scholar, Eric M. ;
Solheim, Joyce C. ;
Singh, Rakesh K. ;
Hoke, Traci A. ;
Talmadge, James E. .
CANCER IMMUNOLOGY IMMUNOTHERAPY, 2010, 59 (01) :47-62
[2]  
Angulo I, 2000, BLOOD, V95, P212
[3]   Myeloid-derived suppressor cells in the peripheral blood of cancer patients contain a subset of immature neutrophils with impaired migratory properties [J].
Brandau, Sven ;
Trellakis, Sokratis ;
Bruderek, Kirsten ;
Schmaltz, Dominik ;
Steller, Gabriele ;
Elian, Motaz ;
Suttmann, Henrik ;
Schenck, Marcus ;
Welling, Juergen ;
Zabel, Peter ;
Lang, Stephan .
JOURNAL OF LEUKOCYTE BIOLOGY, 2011, 89 (02) :311-317
[4]   Myeloid-derived suppressor cells in inflammation: Uncovering cell subsets with enhanced immunosuppressive functions [J].
Bronte, Vincenzo .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2009, 39 (10) :2670-2672
[5]   Inflammation induces myeloid-derived suppressor cells that facilitate tumor progression [J].
Bunt, SK ;
Sinha, P ;
Clements, VK ;
Leips, J ;
Ostrand-Rosenberg, S .
JOURNAL OF IMMUNOLOGY, 2006, 176 (01) :284-290
[6]   Reduced inflammation in the tumor microenvironment delays the accumulation of myeloid-derived suppressor cells and limits tumor progression [J].
Bunt, Stephanie K. ;
Yang, Linglin ;
Sinha, Pratima ;
Clements, Virginia K. ;
Leips, Jeff ;
Ostrand-Rosenberg, Suzanne .
CANCER RESEARCH, 2007, 67 (20) :10019-10026
[7]   Proteomic Pathway Analysis Reveals Inflammation Increases Myeloid-Derived Suppressor Cell Resistance to Apoptosis [J].
Chornoguz, Olesya ;
Grmai, Lydia ;
Sinha, Pratima ;
Artemenko, Konstantin A. ;
Zubarev, Roman A. ;
Ostrand-Rosenberg, Suzanne .
MOLECULAR & CELLULAR PROTEOMICS, 2011, 10 (03)
[8]   Nitroaspirin corrects immune dysfunction in tumor-bearing hosts and promotes tumor eradication by cancer vaccination [J].
De Santo, C ;
Serafini, P ;
Marigo, L ;
Dolcetti, L ;
Bolla, M ;
Del Soldato, P ;
Melani, C ;
Guiducci, C ;
Colombo, MP ;
Iezzi, M ;
Musiani, P ;
Zanovello, P ;
Bronte, V .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (11) :4185-4190
[9]   Increased circulating myeloid-derived suppressor cells correlate with clinical cancer stage, metastatic tumor burden, and doxorubicin-cyclophosphamide chemotherapy [J].
Diaz-Montero, C. Marcela ;
Salem, Mohamed Labib ;
Nishimura, Michael I. ;
Garrett-Mayer, Elizabeth ;
Cole, David J. ;
Montero, Alberto J. .
CANCER IMMUNOLOGY IMMUNOTHERAPY, 2009, 58 (01) :49-59
[10]   Myeloid-derived suppressor cells accumulate in kidney allograft tolerance and specifically suppress effector T cell expansion [J].
Dugast, Anne-Sophie ;
Haudebourg, Thomas ;
Coulon, Flora ;
Heslan, Michele ;
Haspot, Fabienne ;
Poirier, Nicolas ;
de Silly, Romain Vuillefroy ;
Usal, Claire ;
Smit, Helga ;
Martinet, Bernard ;
Thebault, Pamela ;
Renaudin, Karine ;
Vanhove, Bernard .
JOURNAL OF IMMUNOLOGY, 2008, 180 (12) :7898-7906