共 35 条
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
来源:
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.
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页码:790 / 802
页数:13
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