Brichard V, Van Pel A, Wölfel T, Wölfel C, De Plaen E, Lethé B, Coulie P, Boon T
Ludwig Institute for Cancer Research, Brussels Branch, Belgium.
J Exp Med. 1993 Aug 1;178(2):489-95. doi: 10.1084/jem.178.2.489.
Lymphocytes of melanoma patients can be restimulated in vitro with autologous tumor cells to generate antitumor cytolytic T lymphocytes (CTL). Previous reports have indicated that, when such CTL are obtained from HLA-A2 melanoma patients, they often display broad reactivity on A2 melanoma cell lines. Such antitumor CTL clones, which appeared to recognize the same antigen, were isolated from two patients. We report here the cloning of a cDNA that directs the expression of the antigen recognized by these CTL. This cDNA corresponds to the transcript of the tyrosinase gene. The gene was found to be active in all tested melanoma samples and in most melanoma cell lines. Among normal cells, only melanocytes appear to express the gene. The tyrosinase antigen presented by HLA-A2 may therefore constitute a useful target for specific immunotherapy of melanoma. But possible adverse effects of antityrosinase immunization, such as the destruction of normal melanocytes and its consequences, will have to be examined before clinical pilot studies can be undertaken.
黑色素瘤患者的淋巴细胞可以在体外与自体肿瘤细胞一起重新刺激,以产生抗肿瘤细胞溶解T淋巴细胞(CTL)。先前的报告表明,当从HLA - A2黑色素瘤患者获得此类CTL时,它们通常对A2黑色素瘤细胞系表现出广泛的反应性。从两名患者中分离出了似乎识别相同抗原的此类抗肿瘤CTL克隆。我们在此报告了一个cDNA的克隆,该cDNA指导这些CTL识别的抗原的表达。该cDNA对应于酪氨酸酶基因的转录本。发现该基因在所有测试的黑色素瘤样本和大多数黑色素瘤细胞系中都有活性。在正常细胞中,只有黑素细胞似乎表达该基因。因此,由HLA - A2呈递的酪氨酸酶抗原可能构成黑色素瘤特异性免疫治疗的有用靶点。但是在进行临床试点研究之前,必须检查抗酪氨酸酶免疫的可能不良反应,例如正常黑素细胞的破坏及其后果。