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- W2083426921 abstract "Abstract NY‐ESO‐1 is a germ cell antigen aberrantly expressed by different tumor types that elicits strong humoral and cellular immune responses, representing one of the most promising candidates for vaccination of cancer patients. A detailed analysis of CD8 + T cells generated in vaccine trials using NY‐ESO‐1‐derived peptides (157–165 and 157–167) revealed that the dominant immune response was directed against a cryptic epitope (159–167) diverting the immune response from tumor recognition. Only CTL reactivity to the NY‐ESO‐1 157–165 peptide appeared to be capable of lysing NY‐ESO‐1/HLA‐A0201‐expressing tumor cells. To study the process of NY‐ESO‐1 peptide presentation by tumor cells in more detail we generated a high‐affinity (K D =60 nM) antibody fragment that specifically recognizes the NY‐ESO‐1 157–165 peptide/HLA‐A0201 complex. Peptide variants such as the NY‐ESO‐1 157–167 peptide or the cryptic NY‐ESO‐1 159–167 peptide were not recognized. The antibody fragment blocked in a dose‐dependent fashion the recognition of NY‐ESO‐1/HLA‐A2‐positive tumor cells by NY‐ESO‐1 157–165 peptide‐specific CD8 + T cells. This antibody fragment is a novel reagent that binds with TCR‐like specificity to the NY‐ESO‐1 157–165 /HLA‐A2 complex thus distinguishing between CTL responses against immunological meaningful or cryptic NY‐ESO‐1‐derived peptides. It may therefore become a useful monitoring tool for the development of NY‐ESO‐1‐based cancer vaccines." @default.
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- W2083426921 date "2004-08-24" @default.
- W2083426921 modified "2023-10-15" @default.
- W2083426921 title "Dissecting cytotoxic T cell responses towards the NY-ESO-1 protein by peptide/MHC-specific antibody fragments" @default.
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- W2083426921 doi "https://doi.org/10.1002/eji.200425297" @default.
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