Combining radiotherapy and immunotherapy: A revived partnership

被引:290
作者
Demaria, S
Bhardwaj, N
McBride, WH
Formenti, SC
机构
[1] NYU, Sch Med, Inst Canc, Dept Radiat Oncol, New York, NY 10016 USA
[2] NYU, Sch Med, Inst Canc, Dept Pathol, New York, NY 10016 USA
[3] NYU, Sch Med, Inst Canc, Dept Med, New York, NY 10016 USA
[4] Univ Calif Los Angeles, Sch Med, Dept Radiat Oncol, Expt Div, Los Angeles, CA USA
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2005年 / 63卷 / 03期
关键词
ionizing radiation; immunotherapy; cross-priming; tumor-associated antigens;
D O I
10.1016/j.ijrobp.2005.06.032
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Ionizing radiation therapy (RT) is an important local modality for the treatment of cancer. The current rationale for its use is based largely on the ability of RT to kill the cancer cells by a direct cytotoxic effect. Nevertheless, considerable evidence indicates that RT effects extend beyond the mere elimination of the more radiosensitive fraction of cancer cells present within a tumor at the time of radiation exposure. For instance, a large body of evidence is accumulating on the ability of RT to modify the tumor microenvironment and generate inflammation. This might have far-reaching consequences regarding the response of a patient to treatment, especially if radiation-induced tumor cell kill were to translate into the generation of effective antitumor immunity. Although much remains to be learned about how radiation can impact tumor immunogenicity, data from preclinical studies provide the proof of principle that different immunotherapeutic strategies can be combined with RT to enhance antitumor effects. Conversely, RT could be a useful tool to combine with immunotherapy. This article will briefly summarize what is known about the impact of RT on tumor immunity, including tumor-associated antigens, antigen-presenting cells, and effector mechanisms. In addition, the experimental evidence supporting the contention that RT can be used as a tool to induce antitumor immunity is discussed, and a new approach to radioimmunotherapy of cancer is proposed. (c) 2005 Elsevier Inc.
引用
收藏
页码:655 / 666
页数:12
相关论文
共 131 条
[71]   CpG oligodeoxynucleotide enhances tumor response to radiation [J].
Milas, L ;
Mason, KA ;
Ariga, H ;
Hunter, N ;
Neal, R ;
Valdecanas, D ;
Krieg, AM ;
Whisnant, JK .
CANCER RESEARCH, 2004, 64 (15) :5074-5077
[72]   Cross-presentation by intercellular peptide transfer through gap junctions [J].
Neijssen, J ;
Herberts, C ;
Drijfhout, JW ;
Reits, E ;
Janssen, L ;
Neefjes, J .
NATURE, 2005, 434 (7029) :83-88
[73]  
Nikitina EY, 2001, INT J CANCER, V94, P825, DOI 10.1002/1097-0215(20011215)94:6<825::AID-IJC1545>3.0.CO
[74]  
2-5
[75]   A listing of human tumor antigens recognized by T cells: March 2004 update [J].
Novellino, L ;
Castelli, C ;
Parmiani, G .
CANCER IMMUNOLOGY IMMUNOTHERAPY, 2005, 54 (03) :187-207
[76]   Induction of tumor cell apoptosis in vivo increases tumor antigen cross-presentation, cross-priming rather than cross-tolerizing host tumor-specific CD8 T cells [J].
Nowak, AK ;
Lake, RA ;
Marzo, AL ;
Scott, B ;
Heath, WR ;
Collins, EJ ;
Frelinger, JA ;
Robinson, BWS .
JOURNAL OF IMMUNOLOGY, 2003, 170 (10) :4905-4913
[77]   Manipulating dendritic cell biology for the active immunotherapy of cancer [J].
O'Neill, DW ;
Adams, S ;
Bhardwaj, N .
BLOOD, 2004, 104 (08) :2235-2246
[78]   Adenoviral interleukin-3 gene-radiation therapy for prostate cancer in mouse model [J].
Oh, YT ;
Chen, DWC ;
Dougherty, GJ ;
McBride, WH .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2004, 59 (02) :579-583
[79]   The extra domain A of fibronectin activates toll-like receptor 4 [J].
Okamura, Y ;
Watari, M ;
Jerud, ES ;
Young, DW ;
Ishizaka, ST ;
Rose, J ;
Chow, JC ;
Strauss, JF .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (13) :10229-10233
[80]  
Onizuka S, 1999, CANCER RES, V59, P3128