Vaccines against advanced melanoma

被引:16
作者
Blanchard, Tatiana
Srivastava, Pramod K.
Duan, Fei [1 ]
机构
[1] Univ Connecticut, Sch Med, Dept Immunol, Farmington, CT 06030 USA
关键词
CYTOLYTIC T-LYMPHOCYTES; TUMOR-INFILTRATING LYMPHOCYTES; HEAT-SHOCK PROTEINS; ALTERED PEPTIDE LIGANDS; DENDRITIC CELL VACCINE; SOMATIC POINT MUTATION; STAGE-IV MELANOMA; METASTATIC MELANOMA; LUNG-CARCINOMA; ANTIGENIC PEPTIDE;
D O I
10.1016/j.clindermatol.2012.08.005
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100227 [皮肤病学];
摘要
Research shows that cancers are recognized by the immune system but that the immune recognition of tumors does not uniformly result in tumor rejection or regression. Quantitating the success or failure of the immune system in tumor elimination is difficult because we do not really know the total numbers of encounters of the immune system with the tumors. Regardless of that important issue, recognition of the tumor by the immune system implicitly contains the idea of the tumor antigen, which is what is actually recognized. We review the molecular identity of all forms of tumor antigens (antigens with specific mutations, cancer-testis antigens, differentiation antigens, over-expressed antigens) and discuss the use of these multiple forms of antigens in experimental immunotherapy of mouse and human melanoma. These efforts have been uniformly unsuccessful; however, the approaches that have not worked or have somewhat worked have been the source of many new insights into melanoma immunology. From a critical review of the various approaches to vaccine therapy we conclude that individual cancer-specific mutations are truly the only sources of cancer-specific antigens, and therefore, the most attractive targets for immunotherapy. Published by Elsevier Inc.
引用
收藏
页码:179 / 190
页数:12
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