Tumor-associated antigens as tools in immunodiagnostics and immunotherapy of breast cancer

被引:3
|
作者
Gückel, B
Meuer, S
Bastert, G
Wallwiener, D
机构
[1] Univ Tubingen, Frauenklin, D-72076 Tubingen, Germany
[2] Heidelberg Univ, Inst Immunol, D-6900 Heidelberg, Germany
[3] Heidelberg Univ, Frauenklin, D-6900 Heidelberg, Germany
关键词
D O I
10.1055/s-2003-37461
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Recent advances in tumor immunology - such as the characterization of tumor-associated antigens recognized by cellular effectors of the immune system and the improved understanding of antigen processing and presentation - have opened new perspectives on cancer immunotherapy. The most important new approaches are peptide vaccines and whole-cell vaccines (tumor-cell-based or immune-cell-based). The advantage of tumor-cell-based vaccines is that they comprise the complete antigen pool of an individual tumor for activating polyclonal immune responses. The introduction of genes encoding costimulatory molecules or cytokines aims to confer their immunostimulatory potential. The rationale for fusing tumor cells and antigen-presenting cells is that the hybrid cell will display the antigenicity of the tumor and the immunogenicity of the fusion partner. Since the antigenic repertoire of tumor-cell-based Vaccines is usually not fully characterized, it is difficult to estimate their immunostimulatory potential. To be able to assess vaccine-induced immune reactions and clinical responses it Will be necessary to at least partially characterize the antgenicity of cellular vaccines and to define surrogate parameters. The continuously increasing number of HLA-restricted tumor antigens - also identified in breast cancer - allowed the development of antigen-defined vaccines. Direct in vivo administration of peptides in combination with adjuvants suitable for establishing effective immune responses or ex vivo loading of dendritic cells with tumor-specific epitopes are target-specific immunation approaches. Cocktails of synthetic peptide epitopes should permit targeting multiple antigens while avoiding the development of antigen-loss variants. Most clinical phase I/II trials to date indicate that cellular or peptide-based vaccines are safe. But the individual studies are heterogenous and based on small numbers of patients. This review describes advances in vaccination strategies and treatment approaches based on tumor-assocated antigens.
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收藏
页码:130 / 139
页数:10
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