Huang L Q, Brasseur F, Serrano A, De Plaen E, van der Bruggen P, Boon T, Van Pel A
Ludwig Institute for Cancer Research, Brussels Branch, Belgium.
J Immunol. 1999 Jun 1;162(11):6849-54.
From melanoma patient LB1751, cytolytic T lymphocytes (CTL) were generated that lysed specifically autologous tumor cells. To establish whether these CTL recognized one of the Ags that had previously been defined, a CTL clone was stimulated with cells expressing various MAGE genes. It produced TNF upon stimulation with target cells expressing MAGE-A10. The Ag was found to be nonapeptide GLYDGMEHL (codons 254-262), which is presented by HLA-A2.1. This is the first report on the generation of anti-MAGE CTL by autologous mixed lymphocyte-tumor cell culture (MLTC) from a melanoma patient other than patient MZ2, from whom the first MAGE gene was identified. MAGE genes are expressed in many tumors but not by normal tissues except male germline cells and placenta, which do not express HLA molecules. Therefore, the identification of an antigenic peptide derived from MAGE-A10 adds to the repertoire of tumor-specific shared Ags available for anti-tumoral vaccination trials.
从黑色素瘤患者LB1751中产生了能特异性裂解自体肿瘤细胞的细胞毒性T淋巴细胞(CTL)。为确定这些CTL是否识别先前已定义的抗原之一,用表达各种MAGE基因的细胞刺激一个CTL克隆。在用表达MAGE - A10的靶细胞刺激时,它产生了肿瘤坏死因子。发现该抗原为九肽GLYDGMEHL(密码子254 - 262),由HLA - A2.1呈递。这是除了首例MAGE基因被鉴定的患者MZ2之外,关于从黑色素瘤患者通过自体混合淋巴细胞 - 肿瘤细胞培养(MLTC)产生抗MAGE CTL的首次报道。MAGE基因在许多肿瘤中表达,但除了不表达HLA分子的男性生殖系细胞和胎盘外,在正常组织中不表达。因此,源自MAGE - A10的抗原肽的鉴定增加了可用于抗肿瘤疫苗试验的肿瘤特异性共享抗原的种类。