PD-L1-specific T cells

被引:25
作者
Ahmad, Shamaila Munir [1 ]
Borch, Troels Holz [1 ]
Hansen, Morten [1 ]
Andersen, Mads Hald [1 ,2 ]
机构
[1] Copenhagen Univ Hosp, Dept Hematol, CCIT, Herlev Ringvej 75, DK-2730 Herlev, Denmark
[2] Univ Copenhagen, Dept Immunol & Microbiol, Copenhagen, Denmark
关键词
PD-L1; PD-L1-specific T cells; Cancer vaccines; Anti-Tregs; CITIM; 2015; MULTIPLE-MYELOMA; CANCER-IMMUNOTHERAPY; THERAPEUTIC TARGET; ANTI-PD-1; ANTIBODY; IMMUNE SUPPRESSION; B7-H1; EXPRESSION; OVARIAN-CANCER; PD-1; PATHWAY; IFN-GAMMA; B7; FAMILY;
D O I
10.1007/s00262-015-1783-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Recently, there has been an increased focus on the immune checkpoint protein PD-1 and its ligand PD-L1 due to the discovery that blocking the PD-1/PD-L1 pathway with monoclonal antibodies elicits striking clinical results in many different malignancies. We have described naturally occurring PD-L1-specific T cells that recognize both PD-L1-expressing immune cells and malignant cells. Thus, PD-L1-specific T cells have the ability to modulate adaptive immune reactions by reacting to regulatory cells. Thus, utilization of PD-L1-derived T cell epitopes may represent an attractive vaccination strategy for targeting the tumor microenvironment and for boosting the clinical effects of additional anticancer immunotherapy. This review summarizes present information about PD-L1 as a T cell antigen, depicts the initial findings about the function of PD-L1-specific T cells in the adjustment of immune responses, and discusses future opportunities.
引用
收藏
页码:797 / 804
页数:8
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