Õunap Kadri, Kurg Kristiina, Võsa Liisi, Maiväli Ülo, Teras Marina, Planken Anu, Ustav Mart, Kurg Reet
Institute of Technology, University of Tartu, 50411 Tartu, Estonia.
Melanoma Unit of The General Surgery and Oncology Surgery Centre, North Estonian Medical Centre, 13419 Tallinn, Estonia.
Oncol Lett. 2018 Jul;16(1):211-218. doi: 10.3892/ol.2018.8684. Epub 2018 May 10.
Melanoma-associated antigen A (MAGEA) represent a class of tumor antigens that are expressed in a variety of malignant tumors, however, their expression in healthy normal tissues is restricted to germ cells of testis, fetal ovary and placenta. The restricted expression and immunogenicity of these antigens make them ideal targets for immunotherapy in human cancer. In the present study the presence of naturally occurring antibodies against two MAGEA subfamily proteins, MAGEA4 and MAGEA10, was analyzed in patients with melanoma at different stages of disease. Results indicated that the anti-MAGEA4/MAGEA10 immune response in melanoma patients was heterogeneous, with only ~8% of patients having a strong response. Comparing the number of strongly responding patients between different stages of disease revealed that the highest number of strong responses was detected among stage II melanoma patients. These findings support the model that the immune system is involved in the control of melanoma in the early stages of disease.
黑色素瘤相关抗原A(MAGEA)是一类在多种恶性肿瘤中表达的肿瘤抗原,然而,它们在健康正常组织中的表达仅限于睾丸生殖细胞、胎儿卵巢和胎盘。这些抗原的限制性表达和免疫原性使其成为人类癌症免疫治疗的理想靶点。在本研究中,分析了不同疾病阶段黑色素瘤患者中针对两种MAGEA亚家族蛋白MAGEA4和MAGEA10的天然存在抗体。结果表明,黑色素瘤患者中抗MAGEA4/MAGEA10免疫反应具有异质性,只有约8%的患者有强烈反应。比较不同疾病阶段强烈反应患者的数量发现,II期黑色素瘤患者中检测到的强烈反应数量最多。这些发现支持了免疫系统在疾病早期参与黑色素瘤控制的模型。