Targeting Immunotherapy to the Tumor Microenvironment

被引:55
作者
Dougan, Michael [1 ]
Dougan, Stephanie K. [2 ,3 ]
机构
[1] Massachusetts Gen Hosp, Boston, MA 02114 USA
[2] Dana Farber Canc Inst, 450 Brookline Ave,Smith 770A, Boston, MA 02215 USA
[3] Harvard Med Sch, Dept Microbiol & Immunobiol, Boston, MA 02115 USA
关键词
IMMUNOTHERAPY; CANCER IMMUNOLOGY; DRUG TARGETING; TUMOR MICROENVIRONMENT; INFILTRATING MACROPHAGES; PANCREATIC-CANCER; INTERFERON-GAMMA; CELL THERAPY; IMMUNE CELLS; T-CELLS; ANTIBODY; COMBINATION; BLOCKADE; MELANOMA;
D O I
10.1002/jcb.26005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Targeting drugs to the tumor microenvironment has long been appreciated as a means of increasing local concentrations and decreasing systemic toxicities. How drug targeting might apply to immune-based therapies is less clear. In this review, we explain the immunology of cancer, with a focus on the principles of in situ vaccination. Certain types of therapies are more amenable to local versus systemic delivery; these include cytokines, adjuvants, radiation, and agents targeting tumor-resident cell populations. Several approaches for targeting the tumor microenvironment are under development. Nanoparticles, peptide or antibody-based delivery, and exploitation of cellular influx are all promising ways to delivery immune modulating compounds to tumors. (C) 2017 Wiley Periodicals, Inc.
引用
收藏
页码:3049 / 3054
页数:6
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