TY - JOUR
T1 - High-throughput epitope discovery reveals frequent recognition of neo-antigens by CD4(+) T cells in human melanoma
AU - Linnemann, Carsten
AU - van Buuren, Marit M.
AU - Bies, Laura
AU - Verdegaal, Els M. E.
AU - Schotte, Remko
AU - Calis, Jorg J. A.
AU - Behjati, Sam
AU - Velds, Arno
AU - Hilkmann, Henk
AU - Atmioui, Dris El
AU - Visser, Marten
AU - Stratton, Michael R.
AU - Haanen, John B. A. G.
AU - Spits, Hergen
AU - van der Burg, Sjoerd H.
AU - Schumacher, Ton N. M.
PY - 2015
Y1 - 2015
N2 - Tumor-specific neo-antigens that arise as a consequence of mutations(1,2) are thought to be important for the therapeutic efficacy of cancer immunotherapies(3-5). Accumulating evidence suggests that neo-antigens may be commonly recognized by intratumoral CD8(+) T cells(3-7), but it is unclear whether neoantigen-specific CD4(+) T cells also frequently reside within human tumors. In view of the accepted role of tumor-specific CD4(+) T-cell responses in tumor control(8-10), we addressed whether neo-antigen-specific CD4(+) T-cell reactivity is a common property in human melanoma
AB - Tumor-specific neo-antigens that arise as a consequence of mutations(1,2) are thought to be important for the therapeutic efficacy of cancer immunotherapies(3-5). Accumulating evidence suggests that neo-antigens may be commonly recognized by intratumoral CD8(+) T cells(3-7), but it is unclear whether neoantigen-specific CD4(+) T cells also frequently reside within human tumors. In view of the accepted role of tumor-specific CD4(+) T-cell responses in tumor control(8-10), we addressed whether neo-antigen-specific CD4(+) T-cell reactivity is a common property in human melanoma
U2 - https://doi.org/10.1038/nm.3773
DO - https://doi.org/10.1038/nm.3773
M3 - Article
C2 - 25531942
SN - 1078-8956
VL - 21
SP - 81
EP - 85
JO - Nature medicine
JF - Nature medicine
IS - 1
ER -