Luiten R, van der Bruggen P
Ludwig Institute for Cancer Research, Brussels, Belgium.
Tissue Antigens. 2000 Feb;55(2):149-52. doi: 10.1034/j.1399-0039.2000.550206.x.
Antigens encoded by MAGE genes are of particular interest for cancer immunotherapy because of their strict tumoral specificity and because they are shared by many tumors. MAGE antigenic peptides are currently used in therapeutic vaccination trials. The identification of additional antigenic peptides is likely to be important for the future of these clinical trials in order to increase the number of patients eligible for these vaccinations and to analyze in detail the T-cell response of vaccinated patients. We describe here the isolation of a cytolytic T lymphocyte (CTL) clone which recognizes a new MAGE-A1 peptide, RVRFFFPSL (MAGE-A1(289-297)), which is presented by HLA-B7. This CTL clone lysed HLA-B7 tumor cells expressing MAGE-A1. HLA-B7 is expressed by approximately 20% of Caucasians
由于MAGE基因编码的抗原具有严格的肿瘤特异性且为许多肿瘤所共有,因此对癌症免疫疗法具有特殊意义。MAGE抗原肽目前正用于治疗性疫苗试验。鉴定更多的抗原肽可能对这些临床试验的未来发展很重要,以便增加符合这些疫苗接种条件的患者数量,并详细分析接种疫苗患者的T细胞反应。我们在此描述了一种细胞毒性T淋巴细胞(CTL)克隆的分离,该克隆识别一种新的MAGE-A1肽RVRFFFPSL(MAGE-A1(289-297)),它由HLA-B7呈递。该CTL克隆裂解表达MAGE-A1的HLA-B7肿瘤细胞。约20%的高加索人表达HLA-B7