Assessing T-cell responses in anticancer immunotherapy Dendritic cells or myeloid-derived suppressor cells?

被引:18
作者
Escors, David [1 ,2 ]
Liechtenstein, Therese [1 ]
Perez-Janices, Noemi [1 ,2 ]
Schwarze, Julia [3 ]
Dufait, Ines [3 ]
Goyvaerts, Cleo [3 ]
Lanna, Alessio [1 ]
Arce, Frederick [4 ]
Blanco-Luquin, Idoia [2 ]
Kochan, Grazyna [2 ]
Guerrero-Setas, David [2 ]
Breckpot, Karine [3 ]
机构
[1] UCL, Rayne Inst, London, England
[2] Complejo Hosp Navarra, Navarrabiomed Fdn Miguel Servet, Pamplona, Spain
[3] Vrije Univ Brussel, Brussels, Belgium
[4] UCL, Paul OGorman Inst, London, England
关键词
antigen presentation; cancer; dendritic cells; myeloid-derived suppressor cell; T cells; GM-CSF; TUMOR LYSATE; CO-STIMULATION; ANTIGEN; CANCER; ACTIVATION; DIFFERENTIATION; MELANOMA; VIRUS; MODULATION;
D O I
10.4161/onci.26148
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Since dendritic cells operate as professional antigen-presenting cells (APCs) and hence are capable of jumpstarting the immune system, they have been exploited to develop a variety of immunotherapeutic regimens against cancer. In the few past years, myeloid-derived suppressor cells (MDSCs) have been shown to mediate robust immunosuppressive functions, thereby inhibiting tumor-targeting immune responses. Thus, we propose that the immunomodulatory activity of MDSCs should be carefully considered for the development of efficient anticancer immunotherapies.
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页数:9
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共 82 条
[1]   Cotransfection of DC with TLR4 and MART-1 RNA induces MART-1-specific responses [J].
Abdel-Wahab, Z ;
Cisco, R ;
Dannull, J ;
Ueno, T ;
Abdel-Wahab, O ;
Kalady, MF ;
Onaitis, MW ;
Tyler, DS ;
Pruitt, SK .
JOURNAL OF SURGICAL RESEARCH, 2005, 124 (02) :264-273
[2]   Tumor immunotherapy using bone marrow-derived dendritic cells overexpressing Toll-like receptor adaptors [J].
Akazawa, Takashi ;
Shingai, Masashi ;
Sasai, Mwa ;
Ebihara, Takashi ;
Inoue, Norimitsu ;
Matsumoto, Misako ;
Seya, Tsukasa .
FEBS LETTERS, 2007, 581 (18) :3334-3340
[3]   Immortalized myeloid suppressor cells trigger apoptosis in antigen-activated T lymphocytes [J].
Apolloni, E ;
Bronte, V ;
Mazzoni, A ;
Serafini, P ;
Cabrelle, A ;
Segal, DM ;
Young, HA ;
Zanovello, P .
JOURNAL OF IMMUNOLOGY, 2000, 165 (12) :6723-6730
[4]   Selective Activation of Intracellular Signalling Pathways in Dendritic Cells for Cancer Immunotherapy [J].
Arce, Frederick ;
Kochan, Grazyna ;
Breckpot, Karine ;
Stephenson, Holly ;
Escors, David .
ANTI-CANCER AGENTS IN MEDICINAL CHEMISTRY, 2012, 12 (01) :29-39
[5]   Selective ERK Activation Differentiates Mouse and Human Tolerogenic Dendritic Cells, Expands Antigen-Specific Regulatory T Cells, and Suppresses Experimental Inflammatory Arthritis [J].
Arce, Frederick ;
Breckpot, Karine ;
Stephenson, Holly ;
Karwacz, Katarzyna ;
Ehrenstein, Michael R. ;
Collins, Mary ;
Escors, David .
ARTHRITIS AND RHEUMATISM, 2011, 63 (01) :84-95
[6]   Lentivirus-mediated RNA interference of DC-SIGN expression inhibits human immunodeficiency virus transmission from dendritic cells to T cells [J].
Arrighi, JF ;
Pion, M ;
Wiznerowicz, M ;
Geijtenbeek, TB ;
Garcia, E ;
Abraham, S ;
Leuba, F ;
Dutoit, V ;
Ducrey-Rundquist, O ;
van Kooyk, Y ;
Trono, D ;
Piguet, V .
JOURNAL OF VIROLOGY, 2004, 78 (20) :10848-10855
[7]   Enhancing the T-cell stimulatory capacity of human dendritic cells by co-electroporation with CD40L, CD70 and constitutively active TLR4 encoding mRNA [J].
Bonehill, Aude ;
Tuyaerts, Sandra ;
Van Nuffel, An Mt ;
Heirman, Carlo ;
Bos, Tomas J. ;
Fostier, Karel ;
Neyns, Bart ;
Thielemans, Kris .
MOLECULAR THERAPY, 2008, 16 (06) :1170-1180
[8]  
Breckpot Karine, 2009, Endocrine Metabolic & Immune Disorders-Drug Targets, V9, P328
[9]   Attenuated Expression of A20 Markedly Increases the Efficacy of Double-Stranded RNA-Activated Dendritic Cells As an Anti-Cancer Vaccine [J].
Breckpot, Karine ;
Aerts-Toegaert, Cindy ;
Heirman, Carlo ;
Peeters, Uschi ;
Beyaert, Rudi ;
Aerts, Joeri L. ;
Thielemans, Kris .
JOURNAL OF IMMUNOLOGY, 2009, 182 (02) :860-870
[10]   Identification of a CD11b+/Gr-1+/CD31+ myeloid progenitor capable of activating or suppressing CD8+ T cells [J].
Bronte, V ;
Apolloni, E ;
Cabrelle, A ;
Ronca, R ;
Serafini, P ;
Zamboni, P ;
Restifo, NP ;
Zanovello, P .
BLOOD, 2000, 96 (12) :3838-3846