CRCINA, INSERM, Université d'Angers, Université de Nantes, Nantes, France; Laboratoire "Biologie des infections à polyomavirus", ISP1282 INRA Université de Tours, France; Dermatology Department, University of Tours, CHU Tours, Tours, France.
CRCINA, INSERM, Université d'Angers, Université de Nantes, Nantes, France; LabEx IGO "Immunotherapy, Graft, Oncology", Nantes, France.
Cell Immunol. 2019 Oct;344:103961. doi: 10.1016/j.cellimm.2019.103961. Epub 2019 Aug 1.
Merkel cell carcinoma (MCC) is a rare and aggressive cutaneous cancer, which is immunogenic, regardless of the presence of MCPyV (80% of cases). The identification of MCC-specific epitopes recognized by CD8 T cells is crucial to expand the arsenal of immunotherapeutic treatments. Until now, most efforts focused on the identification of virus-specific epitopes, whereas immune responses directed against shared cellular tumor-specific antigens have not been evidenced. In this study, we measured T-cell responses against viral (n = 3) and tumor antigens (n = 47) from TILs derived from 21 MCC tumors. Virus-specific CD8 T-cell responses dominated MCC-specific immune responses, and we identified two new HLA-peptide complexes derived from the LT antigen, located in a region encompassing 3 previously identified epitopes. Finally, we show that MAGE-A3 antigen, frequently expressed by MCC tumors, was recognized by CD8 TILs from a virus-negative MCC tumor and thus could be a target for immunotherapy in this setting.
默克尔细胞癌(Merkel cell carcinoma,MCC)是一种罕见且侵袭性的皮肤癌,具有免疫原性,无论是否存在 MCPyV(80%的病例)。鉴定被 CD8 T 细胞识别的 MCC 特异性表位对于扩大免疫治疗手段至关重要。到目前为止,大多数研究都集中在鉴定病毒特异性表位上,而针对共享细胞肿瘤特异性抗原的免疫反应尚未得到证实。在这项研究中,我们从 21 个 MCC 肿瘤中分离的肿瘤浸润淋巴细胞(TIL)中测量了针对病毒(n=3)和肿瘤抗原(n=47)的 T 细胞反应。病毒特异性 CD8 T 细胞反应主导了 MCC 特异性免疫反应,我们鉴定了两个新的来自 LT 抗原的 HLA-肽复合物,位于先前鉴定的三个表位的一个区域内。最后,我们发现 MCC 肿瘤中经常表达的 MAGE-A3 抗原被来自无病毒 MCC 肿瘤的 CD8 TIL 识别,因此在这种情况下可能成为免疫治疗的靶点。