Therapeutic targeting of myeloid-derived suppressor cells

被引:171
作者
Ugel, Stefano [2 ,3 ]
Delpozzo, Federica [3 ]
Desantis, Giacomo [3 ]
Papalini, Francesca [4 ]
Simonato, Francesca [3 ]
Sonda, Nada [1 ]
Zilio, Serena [2 ,3 ]
Bronte, Vincenzo [1 ]
机构
[1] Ist Oncol Veneto IRCCS, I-35128 Padua, Italy
[2] Dept Oncol & Surg Sci, I-35128 Padua, Italy
[3] Venetian Inst Mol Med, I-35129 Padua, Italy
[4] INRCA IRCCS, Sci Technol Area, Lab Tumor Immunol, I-60121 Ancona, Italy
关键词
ENDOTHELIAL GROWTH-FACTOR; RETINOIC ACID; IMMUNE DYSFUNCTION; CANCER-PATIENTS; TUMOR MICROENVIRONMENT; ANTITUMOR IMMUNITY; OXIDATIVE STRESS; T-CELLS; INHIBITION; MECHANISM;
D O I
10.1016/j.coph.2009.06.014
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Myeloid-derived suppressor cells (MDSCs) represent a subset of myeloid cells that expand under pathological conditions, such as cancer development, acute and chronic infections, trauma, bone marrow transplantations, and some autoimmune diseases. MDSCs mediate a negative regulation of the immune response by affecting different T lymphocyte subsets. Potential mechanisms, which underlie this inhibitory activity range from those requiring direct cell-to-cell contact with others, more indirect, and mediated by the modification of the microenvironment. Pharmacological inhibition of MDSC suppressive pathways is a promising strategy to overcome disease-induced immune defects, which might be a key step in enhancing the effectiveness of immune-based therapies.
引用
收藏
页码:470 / 481
页数:12
相关论文
共 74 条
[1]   Increased production of immature myeloid cells in cancer patients: A mechanism of immunosuppression in cancer [J].
Almand, B ;
Clark, JI ;
Nikitina, E ;
van Beynen, J ;
English, NR ;
Knight, SC ;
Carbone, DP ;
Gabrilovich, DI .
JOURNAL OF IMMUNOLOGY, 2001, 166 (01) :678-689
[2]   Role of tyrosine kinase inhibitors in cancer therapy [J].
Arora, A ;
Scholar, EM .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2005, 315 (03) :971-979
[3]  
Bak AW, 1998, LIFE SCI, V62, pPL367
[4]   Regulation of immune responses by L- arginine metabolism [J].
Bronte, V ;
Zanovello, P .
NATURE REVIEWS IMMUNOLOGY, 2005, 5 (08) :641-654
[5]  
Bronte V, 1999, J IMMUNOL, V162, P5728
[6]   Boosting antitumor responses of T lymphocytes infiltrating human prostate cancers [J].
Bronte, V ;
Kasic, T ;
Gri, G ;
Gallana, K ;
Borsellino, G ;
Marigo, I ;
Battistini, L ;
Iafrate, M ;
Prayer-Galetti, T ;
Pagano, F ;
Viola, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 201 (08) :1257-1268
[7]   L-arginine metabolism in myeloid cells controls T-lymphocyte functions [J].
Bronte, V ;
Serafini, P ;
Mazzoni, A ;
Segal, DM ;
Zanovello, P .
TRENDS IN IMMUNOLOGY, 2003, 24 (06) :302-306
[8]   DEFECTIVE LYMPHOID DEVELOPMENT IN MICE LACKING EXPRESSION OF THE COMMON CYTOKINE RECEPTOR-GAMMA CHAIN [J].
CAO, XQ ;
SHORES, EW ;
HULI, J ;
ANVER, MR ;
KELSALL, BL ;
RUSSELL, SM ;
DRAGO, J ;
NOGUCHI, M ;
GRINBERG, A ;
BLOOM, ET ;
PAUL, WE ;
KATZ, SI ;
LOVE, PE ;
LEONARD, WJ .
IMMUNITY, 1995, 2 (03) :223-238
[9]   Investigation of the binding determinants of phosphopeptides targeted to the Src homology 2 domain of the signal transducer and activator of transcription 3. Development of a high-affinity peptide inhibitor [J].
Coleman, DR ;
Ren, ZY ;
Mandal, PK ;
Cameron, AG ;
Dyer, GA ;
Muranjan, S ;
Campbell, M ;
Chen, XM ;
McMurray, JS .
JOURNAL OF MEDICINAL CHEMISTRY, 2005, 48 (21) :6661-6670
[10]   Cytokine therapy [J].
Cutler, A ;
Brombacher, F .
NATURAL PRODUCTS AND MOLECULAR THERAPY, 2005, 1056 :16-29