Additional unique characteristics were (1) a low baseline titer of antimeasles antibodies; (2) high baseline counts of both measles-reactive and tumor antigen-reactive T cells, and (3) a high mutational burden compared with 664 MM patients whose exome data are publicly available in the Multiple Myeloma Research Foundation CoMMpass Database (NCT 01454297) (Fig. 3c). This evidence concerns the gene LINC01194 and Miyoshi myopathy.