Stimulating Innate Immunity to Enhance Radiation Therapy-Induced Tumor Control

被引:37
作者
Baird, Jason R. [1 ]
Monjazeb, Arta M. [2 ]
Shah, Omid [4 ]
McGee, Heather [5 ]
Murphy, William J. [3 ]
Crittenden, Marka R. [1 ,6 ]
Gough, Michael J. [1 ]
机构
[1] Providence Canc Ctr, Earle A Chiles Res Inst, Portland, OR USA
[2] UC Davis Comprehens Canc Ctr, Dept Radiat Oncol, Sacramento, CA USA
[3] UC Davis Comprehens Canc Ctr, Lab Canc Immunol, Sacramento, CA USA
[4] Stanford Univ, Sch Med, Dept Med, Div Blood & Marrow Transplantat, Stanford, CA 94305 USA
[5] Icahn Sch Med Mt Sinai, Dept Radiat Oncol, New York, NY 10029 USA
[6] Oregon Clin, Portland, OR USA
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2017年 / 99卷 / 02期
关键词
CD8(+) T-CELLS; AGENT 5,6-DIMETHYLXANTHENONE-4-ACETIC ACID; CPG-CONTAINING OLIGODEOXYNUCLEOTIDES; RESECTED PANCREATIC ADENOCARCINOMA; CURE ESTABLISHED TUMORS; ORTHOTOPIC MOUSE MODEL; TOLL-LIKE RECEPTOR-3; IN-SITU VACCINATION; NECROSIS-FACTOR; DENDRITIC CELL;
D O I
10.1016/j.ijrobp.2017.04.014
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Novel ligands that target Toll-like receptors and other innate recognition pathways represent a potent strategy for modulating innate immunity to generate antitumor immunity. Although many of the current clinically successful immunotherapies target adaptive T-cell responses, both preclinical and clinical studies suggest that adjuvants have the potential to enhance the scope and efficacy of cancer immunotherapy. Radiation may be a particularly good partner to combine with innate immune therapies, because it is a highly efficient means to kill cancer cells but may fail to send the appropriate inflammatory signals needed to act as an efficient endogenous vaccine. This may explain why although radiation therapy is a highly used cancer treatment, true abscopal effects-regression of disease outside the field without additional systemic therapy-are extremely rare. This review focuses on efforts to combine innate immune stimuli as adjuvants with radiation, creating a distinct and complementary approach from T cell-targeted therapies to enhance antitumor immunity. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:362 / 373
页数:12
相关论文
共 176 条
[1]
STING Recognition of Cytoplasmic DNA Instigates Cellular Defense [J].
Abe, Takayuki ;
Harashima, Ai ;
Xia, Tianli ;
Konno, Hiroyasu ;
Konno, Keiko ;
Morales, Alejo ;
Ahn, Jeonghyun ;
Gutman, Delia ;
Barber, Glen N. .
MOLECULAR CELL, 2013, 50 (01) :5-15
[2]
Systematic review of case reports on the abscopal effect [J].
Abuodeh, Yazan ;
Venkat, Puja ;
Kim, Sungjune .
CURRENT PROBLEMS IN CANCER, 2016, 40 (01) :25-37
[3]
Topical TLR7 Agonist Imiquimod Can Induce Immune-Mediated Rejection of Skin Metastases in Patients with Breast Cancer [J].
Adams, Sylvia ;
Kozhaya, Lina ;
Martiniuk, Frank ;
Meng, Tze-Chiang ;
Chiriboga, Luis ;
Liebes, Leonard ;
Hochman, Tsivia ;
Shuman, Nicholas ;
Axelrod, Deborah ;
Speyer, James ;
Novik, Yelena ;
Tiersten, Amy ;
Goldberg, Judith D. ;
Formenti, Silvia C. ;
Bhardwaj, Nina ;
Unutmaz, Derya ;
Demaria, Sandra .
CLINICAL CANCER RESEARCH, 2012, 18 (24) :6748-6757
[4]
A novel systemically administered Toll-like receptor 7 agonist potentiates the effect of ionizing radiation in murine solid tumor models [J].
Adlard, Amy L. ;
Dovedi, Simon J. ;
Telfer, Brian A. ;
Koga-Yamakawa, Erina ;
Pollard, Charlotte ;
Honeychurch, Jamie ;
Illidge, Timothy M. ;
Murata, Masashi ;
Robinson, David T. ;
Jewsbury, Philip J. ;
Wilkinson, Robert W. ;
Stratford, Ian J. .
INTERNATIONAL JOURNAL OF CANCER, 2014, 135 (04) :820-829
[5]
Inhibition of Mac-1 (CD11b/CD18) enhances tumor response to radiation by reducing myeloid cell recruitment [J].
Ahn, G-One ;
Tseng, Diane ;
Liao, Cho-Hwa ;
Dorie, Mary Jo ;
Czechowicz, Agnieszka ;
Brown, J. Martin .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (18) :8363-8368
[6]
Recognition of double-stranded RNA and activation of NF-κB by Toll-like receptor 3 [J].
Alexopoulou, L ;
Holt, AC ;
Medzhitov, R ;
Flavell, RA .
NATURE, 2001, 413 (6857) :732-738
[7]
Poly(I:C) as cancer vaccine adjuvant: Knocking on the door of medical breakthroughs [J].
Ammi, Rachid ;
De Waele, Jorrit ;
Willemen, Yannick ;
Van Brussel, Ilse ;
Schrijvers, Dorien M. ;
Lion, Eva ;
Smits, Evelien L. J. .
PHARMACOLOGY & THERAPEUTICS, 2015, 146 :120-131
[8]
Toll-like receptor 4-dependent contribution of the immune system to anticancer chemotherapy and radiotherapy [J].
Apetoh, Lionel ;
Ghiringhelli, Francois ;
Tesniere, Antoine ;
Obeid, Michel ;
Ortiz, Carla ;
Criollo, Alfredo ;
Mignot, Gregoire ;
Maiuri, M. Chiara ;
Ullrich, Evelyn ;
Saulnier, Patrick ;
Yang, Huan ;
Amigorena, Sebastian ;
Ryffel, Bernard ;
Barrat, Franck J. ;
Saftig, Paul ;
Levi, Francis ;
Lidereau, Rosette ;
Nogues, Catherine ;
Mira, Jean-Paul ;
Chompret, Agnes ;
Joulin, Virginie ;
Clavel-Chapelon, Francoise ;
Bourhis, Jean ;
Andre, Fabrice ;
Delaloge, Suzette ;
Tursz, Thomas ;
Kroemer, Guido ;
Zitvogel, Laurence .
NATURE MEDICINE, 2007, 13 (09) :1050-1059
[9]
Treatment of Mammary Carcinomas in HER-2 Transgenic Mice through Combination of Genetic Vaccine and an Agonist of Toll-Like Receptor 9 [J].
Aurisicchio, Luigi ;
Peruzzi, Daniela ;
Conforti, Antonella ;
Dharmapuri, Sridhar ;
Biondo, Antonella ;
Giampaoli, Saverio ;
Fridman, Arthur ;
Bagchi, Ansu ;
Winkelmann, Christopher T. ;
Gibson, Raymond ;
Kandimalla, Ekambar R. ;
Agrawal, Sudhir ;
Ciliberto, Gennaro ;
La Monica, Nicola .
CLINICAL CANCER RESEARCH, 2009, 15 (05) :1575-1584
[10]
A minor population of splenic dendritic cells expressing CD19 mediates IDO-dependent T cell suppression via type IIFN signaling following B7 ligation [J].
Baban, B ;
Hansen, AM ;
Chandler, PR ;
Manlapat, A ;
Bingaman, A ;
Kahler, DJ ;
Munn, DH ;
Mellor, AL .
INTERNATIONAL IMMUNOLOGY, 2005, 17 (07) :909-919