The Basis of Oncoimmunology

被引:665
作者
Palucka, A. Karolina [1 ,2 ]
Coussens, Lisa M. [3 ]
机构
[1] Jackson Lab Genom Med, 10 Discovery Dr, Farmington, CT 06032 USA
[2] Baylor Inst Immunol Res, Dallas, TX 75204 USA
[3] Oregon Hlth & Sci Univ, Knight Canc Inst, Dept Cell Dev & Canc Biol, 3181 SW Sam Jackson Pk Rd,Mail Code L215, Portland, OR 97239 USA
关键词
TUMOR-ASSOCIATED MACROPHAGES; CD4(+) T-CELLS; DENDRITIC CELLS; CHECKPOINT BLOCKADE; CTLA-4; BLOCKADE; STEADY-STATE; HUMAN CANCER; MAST-CELLS; ANTIBODY THERAPY; IFN-GAMMA;
D O I
10.1016/j.cell.2016.01.049
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
Cancer heterogeneity, a hallmark enabling clonal survival and therapy resistance, is shaped by active immune responses. Antigen-specific T cells can control cancer, as revealed clinically by immunotherapeutics such as adoptive T-cell transfer and checkpoint blockade. The host immune system is thus a powerful tool that, if better harnessed, could significantly enhance the efficacy of cytotoxic therapy and improve outcomes for cancer sufferers. To realize this vision, however, a number of research frontiers must be tackled. These include developing strategies for neutralizing tumor-promoting inflammation, broadening T-cell repertoires (via vaccination), and elucidating the mechanisms by which immune cells organize tumor microenvironments to regulate T-cell activity. Such efforts will pave the way for identifying new targets for combination therapies that overcome resistance to current treatments and promote long-term cancer control.
引用
收藏
页码:1233 / 1247
页数:15
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