Tumor-Induced Tolerance and Immune Suppression Depend on the C/EBPβ Transcription Factor

被引:752
作者
Marigo, Ilaria [2 ]
Bosio, Erika [3 ]
Solito, Samantha [2 ]
Mesa, Circe [4 ]
Fernandez, Audry [4 ]
Dolcetti, Luigi [5 ]
Ugel, Stefano [2 ,5 ]
Sonda, Nada [5 ]
Bicciato, Silvio [6 ]
Falisi, Erika [2 ]
Calabrese, Fiorella [3 ]
Basso, Giuseppe [7 ]
Zanovello, Paola [1 ,2 ]
Cozzi, Emanuele [8 ]
Mandruzzato, Susanna [1 ,2 ]
Bronte, Vincenzo [1 ]
机构
[1] IRCCS, IOV, I-35128 Padua, Italy
[2] Univ Padua, Dept Oncol & Surg Sci, I-35128 Padua, Italy
[3] Univ Padua, Dept Med Diagnost Sci & Special Therapies, I-35128 Padua, Italy
[4] Ctr Mol Immunol, Havana 16040, Cuba
[5] Venetian Inst Mol Med, I-35129 Padua, Italy
[6] Univ Modena & Reggio Emilia, Dept Biomed Sci, Ctr Genome Res, I-41100 Modena, Italy
[7] Univ Padua, Dept Pediat, I-35100 Padua, Italy
[8] Padua Hosp, Direz Sanit, I-35128 Padua, Italy
关键词
COLONY-STIMULATING FACTOR; T-CELL RESPONSES; DIFFERENTIATION; ISOFORMS; CANCER; INHIBITION; INDUCTION; SUBSETS; ANTIGEN;
D O I
10.1016/j.immuni.2010.05.010
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Tumor growth is associated with a profound alteration in myelopoiesis, leading to recruitment of immunosuppressive cells known as myeloid-derived suppressor cells (MDSCs). We showed that among factors produced by various experimental tumors, the cytokines GM-CSF, G-CSF, and IL-6 allowed a rapid generation of MDSCs from precursors present in mouse and human bone marrow (BM). BM-MDSCs induced by GM-CSF+IL-6 possessed the highest tolerogenic activity, as revealed by the ability to impair the priming of CD8(+) T cells and allow long term acceptance of pancreatic islet allografts. Cytokines inducing MDSCs acted on a common molecular pathway and the immunoregulatory activity of both tumor-induced and BM-derived MDSCs was entirely dependent on the C/EBP beta transcription factor. Adoptive transfer of tumor antigen-specific CD8(+) T lymphocytes resulted in therapy of established tumors only in mice lacking C/EBP beta in the myeloid compartment, suggesting that C/EBP beta is a critical regulator of the immunosuppressive environment created by growing cancers.
引用
收藏
页码:790 / 802
页数:13
相关论文
共 35 条
[31]   Altered macrophage differentiation and immune dysfunction in tumor development [J].
Sica, Antonio ;
Bronte, Vincenzo .
JOURNAL OF CLINICAL INVESTIGATION, 2007, 117 (05) :1155-1166
[32]   Diagnostic utility of flow cytometric immunophenotyping in myelodysplastic syndrome [J].
Stetler-Stevenson, M ;
Arthur, DC ;
Jabbour, N ;
Xie, XY ;
Molldrem, J ;
Barrett, AJ ;
Venzon, D ;
Rick, ME .
BLOOD, 2001, 98 (04) :979-987
[33]   C/EBP-β mediates iNOS induction by hypoxia in rat pulmonary microvascular smooth muscle cells [J].
Teng, XW ;
Li, DC ;
Catravas, JD ;
Johns, RA .
CIRCULATION RESEARCH, 2002, 90 (02) :125-127
[34]   Autoimmune B-cell lymphopenia after successful adoptive therapy with telomerase-specific T lymphocytes [J].
Ugel, Stefano ;
Scarselli, Elisa ;
Iezzi, Manuela ;
Mennuni, Carmela ;
Pannellini, Tania ;
Calvaruso, Francesco ;
Cipriani, Barbara ;
De Palma, Raffaele ;
Ricci-Vitiani, Lucia ;
Peranzoni, Elisa ;
Musiani, Piero ;
Zanovello, Paola ;
Bronte, Vincenzo .
BLOOD, 2010, 115 (07) :1374-1384
[35]   Subsets of myeloid-derived suppressor cells in tumor-bearing mice [J].
Youn, Je-In ;
Nagaraj, Srinivas ;
Collazo, Michelle ;
Gabrilovich, Dmitry I. .
JOURNAL OF IMMUNOLOGY, 2008, 181 (08) :5791-5802