Opposing Roles of Type I Interferons in Cancer Immunity

被引:132
作者
Boukhaled, Giselle M. [1 ,2 ]
Harding, Shane [1 ,2 ,3 ,4 ]
Brooks, David G. [1 ,2 ]
机构
[1] Univ Hlth Network Toronto, Princess Margaret Canc Ctr, Toronto, ON M5G 2M9, Canada
[2] Univ Toronto, Dept Immunol, Toronto, ON M5S 1A8, Canada
[3] Univ Toronto, Dept Med Biophys, Toronto, ON M5S 1A8, Canada
[4] Univ Toronto, Dept Radiat Oncol, Toronto, ON M5S 1A8, Canada
来源
ANNUAL REVIEW OF PATHOLOGY: MECHANISMS OF DISEASE, VOL 16, 2021 | 2021年 / 16卷
基金
加拿大健康研究院; 美国国家卫生研究院;
关键词
type I interferon; IFN-I; cancer immunology; hallmarks of cancer; immunotherapy; IFN-stimulated gene; ISG; CD8; T-CELLS; ENDOTHELIAL GROWTH-FACTOR; EPITHELIAL-MESENCHYMAL TRANSITION; DENDRITIC CELLS; CHECKPOINT BLOCKADE; PD-1; BLOCKADE; STAGE-III; INDOLEAMINE 2,3-DIOXYGENASE; MAINTENANCE TREATMENT; COLORECTAL-CANCER;
D O I
10.1146/annurev-pathol-031920-093932
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The immune system is tasked with identifying malignant cells to eliminate or prevent cancer spread. This involves a complex orchestration of many immune cell types that together recognize different aspects of tumor transformation and growth. In response, tumors have developed mechanisms to circumvent immune attack. Type I interferons (IFN-Is) are a class of proinflammatory cytokines produced in response to viruses and other environmental stressors. IFN-Is are also emerging as essential drivers of antitumor immunity, potently stimulating the ability of immune cells to eliminate tumor cells. However, a more complicated role for IFN-Is has arisen, as prolonged stimulation can promote feedback inhibitory mechanisms that contribute to immune exhaustion and other deleterious effects that directly or indirectly permit cancer cells to escape immune clearance. We review the fundamental and opposing functions of IFN-Is that modulate tumor growth and impact immune function and ultimately how these functions can be harnessed for the design of new cancer therapies.
引用
收藏
页码:167 / 198
页数:32
相关论文
共 216 条
[1]   Searching for pathogenic gene functions to cervical cancer [J].
Ahn, WS ;
Bae, SM ;
Lee, JM ;
Namkoong, SE ;
Han, SJ ;
Cho, YL ;
Nam, GH ;
Seo, JS ;
Kim, CK ;
Kim, YW .
GYNECOLOGIC ONCOLOGY, 2004, 93 (01) :41-48
[2]   Randomized trial of adjuvant intraperitoneal alpha-interferon in stage III ovarian cancer patients who have no evidence of disease after primary surgery and chemotherapy: An intergroup study [J].
Alberts, DS ;
Hannigan, EV ;
Liu, PY ;
Jiang, C ;
Wilczynski, S ;
Copeland, L ;
Markman, M .
GYNECOLOGIC ONCOLOGY, 2006, 100 (01) :133-138
[3]   IFNB1/interferon-β-induced autophagy in MCF-7 breast cancer cells counteracts its proapoptotic function [J].
Ambjorn, Malene ;
Ejlerskov, Patrick ;
Liu, Yawei ;
Lees, Michael ;
Jaattela, Marja ;
Issazadeh-Navikas, Shohreh .
AUTOPHAGY, 2013, 9 (03) :287-302
[4]   An Analysis of the Expression and Association with Immune Cell Infiltration of the cGAS/STING Pathway in Pan-Cancer [J].
An, Xiang ;
Zhu, Yuanyuan ;
Zheng, Tongsen ;
Wang, Guangyu ;
Zhang, Minghui ;
Li, Jiade ;
Ji, Hongbo ;
Li, Shijun ;
Yang, Shucai ;
Xu, Dandan ;
Li, Zhiwei ;
Wang, Tianzhen ;
He, Yan ;
Zhang, Lei ;
Yang, Weiwei ;
Zhao, Ran ;
Hao, Dapeng ;
Li, Xiaobo .
MOLECULAR THERAPY-NUCLEIC ACIDS, 2019, 14 :80-89
[5]   Type I IFNs induce anti-tumor polarization of tumor associated neutrophils in mice and human [J].
Andzinski, Lisa ;
Kasnitz, Nadine ;
Stahnke, Stephanie ;
Wu, Ching-Fang ;
Gereke, Marcus ;
von Koeckritz-Blickwede, Maren ;
Schilling, Bastian ;
Brandau, Sven ;
Weiss, Siegfried ;
Jablonska, Jadwiga .
INTERNATIONAL JOURNAL OF CANCER, 2016, 138 (08) :1982-1993
[6]   Type 1 Interferon Responses Underlie Tumor-Selective Replication of Oncolytic Measles Virus [J].
Aref, Sarah ;
Castleton, Anna Z. ;
Bailey, Katharine ;
Burt, Richard ;
Dey, Aditi ;
Leongamornlert, Daniel ;
Mitchell, Rachel J. ;
Okasha, Dina ;
Fielding, Adele K. .
MOLECULAR THERAPY, 2020, 28 (04) :1043-1055
[7]   Production of type I interferons: plasmacytoid dendritic cells and beyond [J].
Asselin-Paturel, C ;
Trinchieri, G .
JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 202 (04) :461-465
[8]   Analysis of Apoptosis of Memory T Cells and Dendritic Cells during the Early Stages of Viral Infection or Exposure to Toll-Like Receptor Agonists [J].
Bahl, Kapil ;
Huebner, Anette ;
Davis, Roger J. ;
Welsh, Raymond M. .
JOURNAL OF VIROLOGY, 2010, 84 (10) :4866-4877
[9]   Chromosomal instability drives metastasis through a cytosolic DNA response [J].
Bakhoum, Samuel F. ;
Ngo, Bryan ;
Laughney, Ashley M. ;
Cavallo, Julie-Ann ;
Murphy, Charles J. ;
Ly, Peter ;
Shah, Pragya ;
Sriram, Roshan K. ;
Watkins, Thomas B. K. ;
Taunk, Neil K. ;
Duran, Mercedes ;
Pauli, Chantal ;
Shaw, Christine ;
Chadalavada, Kalyani ;
Rajasekhar, Vinagolu K. ;
Genovese, Giulio ;
Venkatesan, Subramanian ;
Birkbak, Nicolai J. ;
McGranahan, Nicholas ;
Lundquist, Mark ;
LaPlant, Quincey ;
Healey, John H. ;
Elemento, Olivier ;
Chung, Christine H. ;
Lee, Nancy Y. ;
Imielenski, Marcin ;
Nanjangud, Gouri ;
Pe'er, Dana ;
Cleveland, Don W. ;
Powell, Simon N. ;
Lammerding, Jan ;
Swanton, Charles ;
Cantley, Lewis C. .
NATURE, 2018, 553 (7689) :467-+
[10]   Immune Cell-Poor Melanomas Benefit from PD-1 Blockade after Targeted Type I IFN Activation [J].
Bald, Tobias ;
Landsberg, Jennifer ;
Lopez-Ramos, Dorys ;
Renn, Marcel ;
Glodde, Nicole ;
Jansen, Philipp ;
Gaffal, Evelyn ;
Steitz, Julia ;
Tolba, Rene ;
Kalinke, Ulrich ;
Limmer, Andreas ;
Jonsson, Goran ;
Hoelzel, Michael ;
Tueting, Thomas .
CANCER DISCOVERY, 2014, 4 (06) :674-687