Identification of a new HLA-A*0201-restricted T-cell epitope from the tyrosinase-related protein 2 (TRP2) melanoma antigen

For the development of peptide-based immunotherapies, the identification of additional tumor antigens and T-cell epitopes is required. Because HLA-A*0201 is the most common allele in Caucasians, who represent the majority of patients with melanomas, 6 peptides carrying an HLA-A*0201 motif were synth...

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Main Authors: Sun, Yuansheng (Author) , Song, Mingxia (Author) , Paschen, Annette (Author) , Schadendorf, Dirk (Author)
Format: Article (Journal)
Language:English
Published: 10 July 2000
In: International journal of cancer
Year: 2000, Volume: 87, Issue: 3, Pages: 399-404
ISSN:1097-0215
DOI:10.1002/1097-0215(20000801)87:3<399::AID-IJC14>3.0.CO;2-9
Online Access:Verlag, Volltext: http://dx.doi.org/10.1002/1097-0215(20000801)87:3<399::AID-IJC14>3.0.CO;2-9
Verlag, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/1097-0215%2820000801%2987%3A3%3C399%3A%3AAID-IJC14%3E3.0.CO%3B2-9
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Author Notes:Yuansheng Sun, Mingxia Song, Stefan Stevanović, Carsten Jankowiak, Annette Paschen, Hans-Georg Rammensee and Dirk Schadendorf

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520 |a For the development of peptide-based immunotherapies, the identification of additional tumor antigens and T-cell epitopes is required. Because HLA-A*0201 is the most common allele in Caucasians, who represent the majority of patients with melanomas, 6 peptides carrying an HLA-A*0201 motif were synthesized from tyrosinase-related protein-2 (TRP2) melanoma antigen and tested for binding affinity to the HLA allele using processing-defective T2 cells. These peptides were then pulsed onto autologous dendritic cells and used to stimulate in vitro CD8+-enriched T cells isolated from peripheral blood of HLA-A*02+ healthy donors or melanoma patients for the induction of specific cytotoxic T lymphocytes (CTLs). One peptide, TRP2288-296 (SLDDYNHLV), the best HLA-A*0201 binder, elicited specific CTLs from 1 of 4 patients and 3 of 4 healthy donors. The induced CTLs from the patient and from 1 donor efficiently recognized HLA-A*02+ TRP2+ melanomas as well as COS-7 cells expressing HLA-A*0201 and TRP2 in an HLA class I-restricted manner, as assessed by cytokine production and direct cytolysis. The remaining 2 CTL lines derived from 2 donors displayed low T-cell receptor avidity, which could lyse melanoma cells in the presence of exogenous peptide. Since TRP2 is an antigen expressed in most melanomas, identification of the TRP2/HLA-A*0201 peptide SLDDYNHLV may facilitate the design of present peptide-based immunotherapies for the treatment of a large fraction of melanoma patients. 
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