Alves Pedro M S, Lévy Nicole, Bouzourene Hanifa, Viatte Sébastien, Bricard Gabriel, Ayyoub Maha, Vuilleumier Henri, Givel Jean-Claude R, Halkic Nermin, Speiser Daniel E, Romero Pedro, Lévy Frédéric
NCCR, Molecular Oncology, ISREC, Ch. des Boveresses 155, 1066 Epalinges, Switzerland.
Cancer Immunol Immunother. 2007 Jun;56(6):839-47. doi: 10.1007/s00262-006-0228-5. Epub 2006 Sep 8.
Tumor-specific gene products, such as cancer/testis (CT) antigens, constitute promising targets for the development of T cell vaccines. Whereas CT antigens are frequently expressed in melanoma, their expression in colorectal cancers (CRC) remains poorly characterized. Here, we have studied the expression of the CT antigens MAGE-A3, MAGE-A4, MAGE-A10, NY-ESO-1 and SSX2 in CRC because of the presence of well-described HLA-A2-restricted epitopes in their sequences. Our analyses of 41 primary CRC and 14 metastatic liver lesions confirmed the low frequency of expression of these CT antigens. No increased expression frequencies were observed in metastatic tumors compared to primary tumors. Histological analyses of CRC samples revealed heterogeneous expression of individual CT antigens. Finally, evidence of a naturally acquired CT antigen-specific CD8(+) T cell response could be demonstrated. These results show that the expression of CT antigens in a subset of CRC patients induces readily detectable T cell responses.
肿瘤特异性基因产物,如癌胚/睾丸(CT)抗原,是T细胞疫苗开发中很有前景的靶点。虽然CT抗原在黑色素瘤中经常表达,但其在结直肠癌(CRC)中的表达情况仍知之甚少。在此,由于CT抗原MAGE-A3、MAGE-A4、MAGE-A10、NY-ESO-1和SSX2的序列中存在已明确描述的HLA-A2限制性表位,我们对其在CRC中的表达进行了研究。我们对41例原发性CRC和14例转移性肝病灶的分析证实了这些CT抗原的低表达频率。与原发性肿瘤相比,转移性肿瘤中未观察到表达频率增加。CRC样本的组织学分析显示单个CT抗原的表达具有异质性。最后,可以证明存在自然获得的CT抗原特异性CD8(+) T细胞反应。这些结果表明,CT抗原在一部分CRC患者中的表达可诱导易于检测到的T细胞反应。