Cancer Immunology Miniatures Spontaneous Peripheral T-cell Responses toward the Tumor-Associated Antigen Cyclin D1 in Patients with Clear Cell Renal Cell Carcinoma

نویسندگان

  • Stefanie R. Dannenmann
  • Thomas Hermanns
  • Ali Bransi
  • Claudia Matter
  • Lotta von Boehmer
  • Stefan Stevanovic
  • Peter Schraml
  • Holger Moch
  • Alexander Knuth
  • Maries van den Broek
چکیده

Renal cell carcinoma (RCC) is a heterogeneous groupof kidney cancerswith clear cell RCC (ccRCC) as themajor subgroup. To expand the number of clinically relevant tumor-associated antigens (TAA) that can be targeted by immunotherapy, we analyzed samples from 23 patients with primary ccRCC for the expression and immunogenicity of various TAAs. We found high-frequency expression of MAGE-A9 and NY-ESO-1 in 36% and 55% of samples, respectively, and overexpression of PRAME, RAGE-1, CA-IX, Cyclin D1, ADFP, C-MET, and RGS-5 in many of the tumor samples. We analyzed the blood of patients with HLA-A2þ ccRCC for the presence of CD8þ T cells specific for TAA-derived HLA-A2–restricted peptides and found spontaneous responses to cyclin D1 in 5 of 6 patients with Cyclin D1–positive tumors. Cyclin D1–specific CD8þ T cells secreted TNF-a, IFN-g , and interleukin2 (IL-2), and degranulated, indicating the presence of polyfunctional tumor-specific CD8þ T cells in the blood of these patients with ccRCC. The high frequency (43%) of Cyclin D1 overexpression and the presence of functional cyclin D1–specific T cells in 83% of these patients with ccRCC suggest that cyclin D1 may be a target for immunotherapeutic strategies. Cancer Immunol Res; 1(5); 288–95. 2013 AACR.

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تاریخ انتشار 2013