Reorienting the immune system in the treatment of cancer by using anti-PD-1 and anti-PD-L1 antibodies

被引:33
作者
Borch, Troels H. [1 ,2 ]
Donia, Marco [1 ,2 ]
Andersen, Mads H. [1 ]
Svane, Inge M. [1 ,2 ]
机构
[1] Univ Copenhagen, Herlev Hosp, Dept Hematol, CCIT, Copenhagen, Denmark
[2] Univ Copenhagen, Herlev Hosp, Dept Oncol, Copenhagen, Denmark
关键词
T-CELL-ACTIVATION; PHASE-I; PD-1; BLOCKADE; METASTATIC MELANOMA; NIVOLUMAB ANTI-PD-1; CLINICAL ACTIVITY; OPEN-LABEL; SAFETY; EXPRESSION; IPILIMUMAB;
D O I
10.1016/j.drudis.2015.07.003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Physiologically, the programmed death 1 (PD-1) pathway is involved in limiting the killing of bystander cells during an infection and controlling autoimmunity. However, cancers exploit this system to avoid immune killing, and PD-1 ligand 1 and 2 (PD-L1 and PD-L2) expression on tumor cells, as well as PD-1 expression on tumor-infiltrating lymphocytes, have shown to be negative prognostic factors. Promising clinical results have been obtained by PD-1 pathway blockade in a range of cancers while still maintaining a manageable toxicity profile, and two anti-PD-1 antibodies are now approved by the US Food and Drug Administration (FDA) for the treatment of metastatic melanoma. As already shown with nivolumab and ipilimumab, the combination of PD-1 pathway blockade with other anticancer agents holds promise in the form of additive synergistic anticancer effects.
引用
收藏
页码:1127 / 1134
页数:8
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