Ayyoub Maha, Hesdorffer Charles S, Montes Monica, Merlo Andrea, Speiser Daniel, Rimoldi Donata, Cerottini Jean-Charles, Ritter Gerd, Scanlan Matthew, Old Lloyd J, Valmori Danila
Ludwig Institute Clinical Trial Center, Columbia University College of Physicians and Surgeons, New York, NY 10032, USA.
J Clin Invest. 2004 Apr;113(8):1225-33. doi: 10.1172/JCI20667.
Ectopic gene expression in tumors versus normal somatic tissues provides opportunities for the specific immunotargeting of cancer cells. SSX gene products are expressed in tumors of different histological types and can be recognized by tumor-reactive CTLs from cancer patients. Here, we report the identification of an SSX-2-derived immunodominant T cell epitope recognized by CD4(+) T cells from melanoma patients in association with HLA-DR. The epitope maps to the 37-58 region of the protein, encompassing the sequence of the previously defined HLA-A2-restricted immunodominant epitope SSX-2(41-49). SSX-2(37-58)-specific CD4(+) T cells were detected among circulating lymphocytes from the majority of melanoma patients analyzed and among tumor-infiltrating lymphocytes, but not in healthy donors. Together, our data suggest a dominant role of the 37-58 sequence in the induction of cellular CD4(+) T cell responses against SSX antigens and will be instrumental for both the onset and the monitoring of upcoming cancer-vaccine trials using SSX-derived immunogens.
肿瘤与正常体细胞组织中的异位基因表达为癌细胞的特异性免疫靶向提供了机会。SSX基因产物在不同组织学类型的肿瘤中表达,并且可被癌症患者的肿瘤反应性CTL识别。在此,我们报告了鉴定出一个源自SSX-2的免疫显性T细胞表位,该表位可被黑色素瘤患者的CD4(+) T细胞与HLA-DR结合识别。该表位定位于蛋白质的37-58区域,包含先前定义的HLA-A2限制性免疫显性表位SSX-2(41-49)的序列。在分析的大多数黑色素瘤患者的循环淋巴细胞以及肿瘤浸润淋巴细胞中检测到了SSX-2(37-58)特异性CD4(+) T细胞,但在健康供体中未检测到。总之,我们的数据表明37-58序列在诱导针对SSX抗原的细胞CD4(+) T细胞反应中起主导作用,并且对于使用源自SSX的免疫原进行即将到来的癌症疫苗试验的启动和监测都将有帮助。