Giulia Tirloni, Viola Chiavetta, Juliette Villemonteix, Debora Jorge-Cordeiro, Giovanni Grillo, Roberto Cairoli, Giulia Di Maggio, Giorgia Cornacchini, Laurie Toullec, Sophie Caillat-Zucman, Vincent Allain, Antonio Milano, Elisabetta Volpato, Roberto Crocchiolo
HLA Evolutionary Divergence (HED) measures the structural differences between alleles at a single locus reflecting the immunopeptidome. While high HED is associated with better T-cell responses against pathogens and tumors, its role in determining initial susceptibility to Cytomegalovirus (CMV) remains unexplored. We analyzed HLA typing and CMV IgG data from 526 adult HSCT patients and their donors at the ASST Grande Ospedale Metropolitano Niguarda (1987-2023). HED was calculated using the Grantham distance for HLA-A, B, C, -DRB1, -DQB1, and -DPB1. We compared HED scores between CMV-seropositive (IgG+) and seronegative (IgG-) individuals using the Mann-Whitney U test to determine if HLA divergence influences initial viral susceptibility. The results showed no statistically significant differences across individual loci or grouped Class I and II HED scores, indicating no correlation between HED and CMV serological status. The lack of correlation with serostatus does not rule out HED's clinical utility. Given that HLA-specific binding to ppo5 and IEl is vital for viral control, future research should investigate if HED affects CMV reactivation post-transplant. Expanding this analysis to larger, multicenter datasets will help determine if HLA divergence serves as a viable prognostic marker for HSCT outcomes.