Olsson Anna-Karin
*Department of Medical Biochemistry and Microbiology, Science for Life Laboratory, Uppsala University, Biomedical Center, Box 582, SE-75123 Uppsala, Sweden.
Biochem Soc Trans. 2014 Dec;42(6):1653-7. doi: 10.1042/BST20140196.
Therapeutic vaccination targeting self-molecules could provide a cost-efficient alternative to monoclonal antibody-based therapies for cancer and various inflammatory diseases. However, development of cancer vaccines targeting self-molecules has proven difficult. One complicating factor is that tumour cells have developed strategies to escape recognition by the immune system. Antigens specifically expressed by the tumour vasculature can therefore provide alternative targets. The present mini-review highlights potential target molecules associated with tumour angiogenesis and the approaches made to direct an immune response against them. Furthermore, the requirements on a vaccine targeting self-molecules, in contrast with those directed against virus or bacteria, are discussed.
针对自身分子的治疗性疫苗可为癌症和各种炎症性疾病提供一种比基于单克隆抗体的疗法更具成本效益的替代方案。然而,事实证明,开发针对自身分子的癌症疫苗颇具难度。一个复杂因素是肿瘤细胞已形成逃避免疫系统识别的策略。因此,肿瘤血管特异性表达的抗原可提供替代靶点。本小型综述重点介绍了与肿瘤血管生成相关的潜在靶分子以及针对这些分子引发免疫反应的方法。此外,还讨论了针对自身分子的疫苗与针对病毒或细菌的疫苗相比的要求。