Context-Specific Determinants of the Immunosuppressive Tumor Microenvironment in Pancreatic Cancer

被引:109
作者
Falcomata, Chiara [1 ,2 ,3 ,4 ,5 ]
Baerthel, Stefanie [1 ,2 ,3 ,4 ,5 ]
Schneider, Guenter [1 ,2 ,3 ,4 ,5 ,6 ]
Rad, Roland [2 ,5 ,7 ]
Schmidt-Supprian, Marc [2 ,5 ,8 ]
Saur, Dieter [1 ,2 ,3 ,4 ,5 ]
机构
[1] German Canc Res Ctr, Div Translat Canc Res, Heidelberg, Germany
[2] German Canc Consortium DKTK, Heidelberg, Germany
[3] Tech Univ Munich, Chair Translat Canc Res, Sch Med, Klinikum Rechts Isar, Munich, Germany
[4] Tech Univ Munich, Inst Expt Canc Therapy, Sch Med, Klinikum Rechts Isar, Munich, Germany
[5] Tech Univ Munich, Ctr Translat Canc Res TranslaTUM, Sch Med, Munich, Germany
[6] Univ Med Ctr Gottingen, Dept Gen Visceral & Pediat Surg, Gottingen, Germany
[7] Tech Univ Munich, Inst Mol Oncol & Funct Genom, Sch Med, Munich, Germany
[8] Tech Univ Munich, Inst Expt Hematol, Sch Med, Munich, Germany
基金
欧洲研究理事会;
关键词
REGULATORY T-CELLS; ENDOTHELIAL GROWTH-FACTOR; DUCTAL ADENOCARCINOMA; INFILTRATING MACROPHAGES; INDUCED INFLAMMATION; SUPPRESSOR-CELLS; IMMUNE-RESPONSE; OPEN-LABEL; EXPRESSION; IMMUNOTHERAPY;
D O I
10.1158/2159-8290.CD-22-0876
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Immunotherapies have shown benefits across a range of human cancers, but not pancreatic ductal adenocarcinoma (PDAC). Recent evidence suggests that the immunosuppressive tumor microenvironment (TME) constitutes an important roadblock to their effi-cacy. The landscape of the TME differs substantially across PDAC subtypes, indicating context-specific principles of immunosuppression. In this review, we discuss how PDAC cells, the local TME, and sys-temic host and environmental factors drive immunosuppression in context. We argue that unraveling the mechanistic drivers of the context-specific modes of immunosuppression will open new possibili-ties to target PDAC more efficiently by using multimodal (immuno)therapeutic interventions. Significance: Immunosuppression is an almost universal hallmark of pancreatic cancer, although this tumor entity is highly heterogeneous across its different subtypes and phenotypes. Here, we provide evidence that the diverse TME of pancreatic cancer is a central executor of various different context -dependent modes of immunosuppression, and discuss key challenges and novel opportunities to uncover, functionalize, and target the central drivers and functional nodes of immunosuppression for therapeutic exploitation.
引用
收藏
页码:278 / 297
页数:20
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