Tumor-directed immunotherapy can generate tumor-specific T cell responses through localized co-stimulation

被引:28
作者
Ellmark, Peter [1 ,2 ]
Mangsbo, Sara M. [3 ]
Furebring, Christina [1 ]
Norlen, Per [1 ]
Totterman, Thomas H. [3 ]
机构
[1] Alligator Biosci AB, S-22363 Lund, Sweden
[2] Lund Univ, Dept Immunotechnol, Lund, Sweden
[3] Uppsala Univ, Dept Immunol Genet & Pathol, Uppsala, Sweden
关键词
Immunotherapy; Tumor-directed immunotherapy; Cancer; Intratumoral; Bispecific antibody; Immuno-oncology; IN-SITU VACCINATION; FC-GAMMA-RIIB; BISPECIFIC ANTIBODIES; CANCER-IMMUNOTHERAPY; THERAPY; IMMUNOCYTOKINES; COMBINATION; ACTIVATION; STRATEGIES; DEPLETION;
D O I
10.1007/s00262-016-1909-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The most important goals for the field of immuno-oncology are to improve the response rate and increase the number of tumor indications that respond to immunotherapy, without increasing adverse side effects. One approach to achieve these goals is to use tumor-directed immunotherapy, i.e., to focus the immune activation to the most relevant part of the immune system. This may improve anti-tumor efficacy as well as reduce immune-related adverse events. Tumor-directed immune activation can be achieved by local injections of immune modulators in the tumor area or by directing the immune modulator to the tumor using bispecific antibodies. In this review, we focus on therapies targeting checkpoint inhibitors and co-stimulatory receptors that can generate tumor-specific T cell responses through localized immune activation.
引用
收藏
页码:1 / 7
页数:7
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