As these often arise from driver mutations, they are expected to be clonal and recur between patients. To identify new hotspot neoantigens, we developed a data-driven strategy for scanning recurrent neoantigens in melanoma using immunopeptidomics. Using this approach, we have already identified novel MHC-presented neoantigens derived from NRASQ61K, NRASQ61R, PIK3CAE545 and KRASG12V. Importantly, our identification of the neoantigen cognate TCRs allows for an 'off-the shelf' treatment pan-cancer.
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