A natural cytotoxic T cell response in a spontaneously regressing human melanoma targets a neoantigen resulting from a somatic point mutation

Abstract

We have studied a case of human primary melanoma displaying the classical signs of a spontaneous regression in order to characterize potentially efficient anti‐tumor T cell responses. In a previous series of experiments a unique TCR Vβ16⁺ T cell was shown to be highly expanded at the tumor site. The corresponding clone was isolated in vitro and found to be a CD8⁺ cytotoxic T lymphocyte with a strong and selective cytolytic activity against the autologous tumor cell line. Here, we demonstrate that this predominant Vβ16⁺ tumor‐infiltrating lymphocyte recognizes a peptide encoded by a novel unconventional myosin class I gene. This peptide includes a mutation due to a single nucleotide substitution. The resulting Glu → Lys replacement at position 911 of the coding sequence is critical to generate the recognized T cell epitope. These experiments demonstrate the existence of a natural tumor‐specific cytolytic T cell response in a primary regressing human melanoma lesion.