Trafficking of T Cells into Tumors

被引:316
作者
Slaney, Clare Y. [1 ,2 ,3 ]
Kershaw, Michael H. [1 ,2 ,3 ,4 ]
Darcy, Phillip K. [1 ,2 ,3 ,4 ]
机构
[1] Peter MacCallum Canc Ctr, Canc Immunol Program, East Melbourne, Vic, Australia
[2] Univ Melbourne, Dept Pathol, Parkville, Vic 3052, Australia
[3] Univ Melbourne, Sir Peter MacCallum Dept Oncol, Parkville, Vic 3052, Australia
[4] Monash Univ, Dept Immunol, Clayton, Vic, Australia
基金
澳大利亚国家健康与医学研究理事会; 英国医学研究理事会;
关键词
BREAST-CANCER; INFILTRATING LYMPHOCYTES; ADOPTIVE IMMUNOTHERAPY; IMMUNE CELLS; ESTABLISHED TUMORS; ANTI-PD-1; ANTIBODY; SOLID TUMORS; EXPRESSION; THERAPY; RECEPTOR;
D O I
10.1158/0008-5472.CAN-14-2458
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
T cells are a crucial component of the immune response to infection and cancer. In addition to coordinating immunity in lymphoid tissue, T cells play a vital role at the disease site, which relies on their efficient and specific trafficking capabilities. The process of T-cell trafficking is highly dynamic, involving a series of distinct processes, which include rolling, adhesion, extravasation, and chemotaxis. Trafficking of T cells to the tumor microenvironment is critical for the success of cancer immunotherapies such as adoptive cellular transfer. Although this approach has achieved some remarkable responses in patients with advanced melanoma and hematologic malignancy, the success against solid cancers has been more moderate. One of the major challenges for adoptive immunotherapy is to be able to effectively target a higher frequency of T cells to the tumor microenvironment, overcoming hurdles associated with immunosuppression and aberrant vasculature. This review summarizes recent advances in our understanding of T-cell migration in solid cancer and immunotherapy based on the adoptive transfer of natural or genetically engineered tumor-specific T cells and discusses new strategies that may enhance the trafficking of these cells, leading to effective eradication of solid cancer and metastases. (C)2014 AACR.
引用
收藏
页码:7168 / 7174
页数:7
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