Targeting cytotoxic T-lymphocyte antigen 4 in immunotherapies for melanoma and other cancers

被引:3
|
作者
Page, David B. [1 ,2 ]
Yuan, Jianda [3 ]
Wolchok, Jedd D. [1 ,3 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Melanoma Sarcoma Serv, New York, NY 10021 USA
[2] Columbia Univ, Med Ctr, New York Presbyterian Hosp, New York, NY 10027 USA
[3] Sloan Kettering Inst, Ludwig Ctr Canc Immunotherapy, New York, NY USA
关键词
cytotoxic T-lymphocyte antigen 4 blockade; immune surveillance; immunoediting; immunogram; immunotherapy; ipilimumab; melanoma; tremelimumab; PHASE-I TRIAL; CTLA-4; BLOCKADE; COMBINATION IMMUNOTHERAPY; METASTATIC MELANOMA; MONOCLONAL-ANTIBODY; CELL RESPONSES; ANTITUMOR IMMUNITY; TUMOR-REGRESSION; PROSTATE-CANCER; MOUSE MODEL;
D O I
10.2217/IMT.10.21
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The immune system can simultaneously protect against tumor growth and sculpt resistant tumor strains. By a variety of mechanisms, anti-cytotoxic T-lymphocyte antigen (CTLA)-4 therapy may shift such opposing forces towards tumor elimination. In recent clinical trials, anti-CTLA-4 therapy induces durable responses that correlate with markers of immune activity, such as antigen-specific CD4(+) or CD8(+) cytokine release, antitumor antibody formation or cellular phenotype differentiation. However, some patients exhibit atypical responses to anti-CTLA-4 therapy, demonstrating transient/delayed responses or heterogeneity by lesion site. Such atypical responses may offer insight into the mechanism of anti-CTLA-4 therapy. The immunogram a newly described graphical synthesis of treatment data and immune correlates in individual patients may help us to confirm, reject or formulate new hypotheses regarding the mechanism of anti-CTLA-4 activity.
引用
收藏
页码:367 / 379
页数:13
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