Bakker A B, Schreurs M W, Tafazzul G, de Boer A J, Kawakami Y, Adema G J, Figdor C G
Department of Tumor Immunology, University Hospital Nijmegen St. Radboud, The Netherlands.
Int J Cancer. 1995 Jul 4;62(1):97-102. doi: 10.1002/ijc.2910620118.
Cytotoxic T lymphocytes (CTL) reactive with human melanoma tumor cells occasionally display cross-reactivity with normal melanocytes. Previously, we identified the melanocyte lineage-specific antigen gp 100 that is expressed by both melanoma cells and normal melanocytes, as a target antigen for tumor-infiltrating lymphocytes derived from a melanoma patient (TIL 1200). Here, we demonstrate that the oligoclonal HLA-A2.1-restricted TIL 1200 line is reactive with 2 distinct peptides derived from the gp 100 protein. Apart from the peptide corresponding to gp 100 amino acids 457-466, we identified the gp 100 peptide 154-162 as a second epitope recognized by TIL 1200. A 100-fold lower concentration of this novel gp 100 peptide was required for target-cell sensitization compared to peptide 457-466, indicating that the 154-162 peptide is the dominant gp 100 epitope for TIL 1200. Together with the recently described gp 100 280-288 epitope, 3 distinct CTL epitopes have now been identified in gp 100, all presented in the context of HLA-A2.1. Therefore, gp 100 is an attractive target antigen in the development of immuno-therapeutic protocols against melanoma.
与人类黑色素瘤肿瘤细胞发生反应的细胞毒性T淋巴细胞(CTL)偶尔会与正常黑素细胞表现出交叉反应性。此前,我们鉴定出黑色素细胞谱系特异性抗原gp 100,其由黑色素瘤细胞和正常黑素细胞共同表达,作为一名黑色素瘤患者(TIL 1200)来源的肿瘤浸润淋巴细胞的靶抗原。在此,我们证明寡克隆的HLA - A2.1限制性TIL 1200细胞系与源自gp 100蛋白的2种不同肽段发生反应。除了对应于gp 100氨基酸457 - 466的肽段外,我们鉴定出gp 100肽段154 - 162是TIL 1200识别的第二个表位。与肽段457 - 466相比,该新型gp 100肽段用于靶细胞致敏所需的浓度低100倍,表明154 - 162肽段是TIL 1200的主要gp 100表位。连同最近描述的gp 100 280 - 288表位,现已在gp 100中鉴定出3种不同的CTL表位,均在HLA - A2.1背景下呈递。因此,gp 100在针对黑色素瘤的免疫治疗方案开发中是一个有吸引力的靶抗原。