Mapping early β‑cell changes and immune interactions in type 1 diabetes progression
A large-scale imaging mass cytometry study of 88 human pancreata across the type 1 diabetes spectrum profiles 16 million cells to map β-cell states and the islet–immune interface. It finds β-cells show IAPP loss in preclinical stages and increased MHC-I at onset, with no universal rise in selected ER-stress markers. Insulitic islets display IFN signatures. Early disease features include pro‑inflammatory M1/M2‑like macrophages and exhausted‑like PD1+ TIM3+ T cells whose interactions occur at the islet edge and within islets, suggesting antigen presentation and regulatory dynamics. Age-related motifs reveal more TLS-like B/T cell structures and CD11c+ macrophages in younger donors. Pseudotime analysis suggests a single trajectory from healthy to insulitic β-cells, driven by macrophage–DC–exhausted T cell axis as disease progresses. The work provides a rich resource for understanding early T1D progression and identifying potential therapeutic targets and biomarkers.
