Department of Immunology, Institute of Cell Biology, and German Cancer Consortium (DKTK), German Cancer Research Center (DKFZ) Partner Site Tübingen, Auf der Morgenstelle 15, 72076 Tübingen, Germany.
Expert Rev Vaccines. 2013 Oct;12(10):1211-7. doi: 10.1586/14760584.2013.836911. Epub 2013 Oct 4.
Every cancer is different and cancer cells differ from normal cells, in particular, through genetic alterations. HLA molecules on the cell surface enable T lymphocytes to recognize cellular alterations as antigens, including mutations, increase in gene product copy numbers or expression of genes usually not used in the adult organism. The search for cancer-associated antigens shared by many patients with a particular cancer has yielded a number of hits used in clinical vaccination trials with indication of survival benefit. Targeting cancer-specific antigens, which are exclusively expressed on cancer cells and not on normal cells, holds the promise for much better results and perhaps even a cure. Such antigens, however, may specifically appear in very few patients or may be mutated appearing just in one patient. Therefore, to target these in a molecularly defined way, the approach has to be individualized.
每种癌症都是不同的,癌细胞与正常细胞也不同,特别是在遗传改变方面。细胞表面的 HLA 分子使 T 淋巴细胞能够识别细胞改变作为抗原,包括突变、基因产物拷贝数增加或通常在成年生物体中不使用的基因表达。寻找许多特定癌症患者共有的癌症相关抗原已产生了一些在具有生存获益指示的临床疫苗试验中使用的命中。针对仅在癌细胞上表达而不在正常细胞上表达的癌症特异性抗原具有产生更好结果甚至治愈的潜力。然而,这些抗原可能仅在极少数患者中特异性出现,或者可能在一个患者中发生突变。因此,为了以分子定义的方式针对这些抗原,该方法必须个体化。