Rationale for immune-based therapies in Merkel polyomavirus-positive and -negative Merkel cell carcinomas

被引:16
|
作者
Vandeven, Natalie [1 ]
Nghiem, Paul [1 ]
机构
[1] Univ Washington, Dept Med Pathol & Dermatol, Seattle, WA 98195 USA
基金
美国国家卫生研究院;
关键词
exhaustion; immune evasion; immune therapy; Merkel cell carcinoma; Merkel cell polyomavirus; PD-1; PD-L1; SMALL T-ANTIGEN; CHRONIC LYMPHOCYTIC-LEUKEMIA; PROGRAMMED DEATH-1 LIGAND-1; E-SELECTIN EXPRESSION; PD-1; BLOCKADE; INDEPENDENT PREDICTOR; MONOCLONAL-ANTIBODY; CTLA-4; LATEST EVIDENCE; DOWN-REGULATION;
D O I
10.2217/imt-2016-0009
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Merkel cell carcinoma (MCC) is a rare but often deadly skin cancer that is typically caused by the Merkel cell polyomavirus (MCPyV). Polyomavirus T-antigen oncoproteins are persistently expressed in virus-positive MCCs (similar to 80% of cases), while remarkably high numbers of tumor-associated neoantigens are detected in virus-negative MCCs, suggesting that both MCC subsets may be immunogenic. Here we review mechanisms by which these immunogenic tumors evade multiple levels of host immunity. Additionally, we summarize the exciting potential of diverse immune-based approaches to treat MCC. In particular, agents blocking the PD-1 axis have yielded strikingly high response rates in MCC as compared with other solid tumors, highlighting the potential for immune-mediated treatment of this disease.
引用
收藏
页码:907 / 921
页数:15
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