Directing Traffic: How to Effectively Drive T Cells into Tumors

被引:82
作者
Anandappa, Annabelle J. [1 ,2 ,3 ]
Wu, Catherine J. [1 ,2 ,4 ,5 ]
Ott, Patrick A. [1 ,2 ,4 ,5 ]
机构
[1] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[2] Harvard Med Sch, Boston, MA 02115 USA
[3] Massachusetts Gen Hosp, Dept Med, Boston, MA 02114 USA
[4] Brigham & Womens Hosp, Dept Med, 75 Francis St, Boston, MA 02115 USA
[5] Broad Inst MIT & Harvard, Cambridge, MA 02142 USA
关键词
PD-1; BLOCKADE; BRAF INHIBITION; BREAST-CANCER; COMBINATION IMMUNOTHERAPY; INFILTRATING LYMPHOCYTES; ANTITUMOR IMMUNITY; STING PATHWAY; MELANOMA; MICROENVIRONMENT; RESISTANCE;
D O I
10.1158/2159-8290.CD-19-0790
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Although immune checkpoint inhibitors (ICI) have demonstrated clinical activity in multiple tumor types, the majority of patients do not respond to ICI monotherapy. Mounting evidence suggests that ICI-mediated clinical responses rely upon tumor infiltration by T cells that are able to recognize and kill cancer cells. Here, we review therapeutic modalities that have been shown to promote T-cell infiltration into human tumors in studies to date, and discuss emerging data guiding how these modalities can be sequenced in order to optimize T-cell effector function and memory T-cell generation, while minimizing overactivation and potential toxicity. Significance:The lack of preexisting T-cell inflammation in tumors is a major barrier to effective cancer immunity. A deep understanding of the mechanisms that prevent T cells from trafficking into the tumor in a given individual will be critical for tailoring immunotherapy combinations that can overcome resistance to ICI in patients with cancer.
引用
收藏
页码:185 / 197
页数:13
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