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Niotis, G.* ; Arvanitaki, E.S.* ; Theodorakis, E.* ; Schmalen, A. ; Juretschke, T.* ; Argyros, O.* ; Tsolis, K.C.* ; Bertsias, G.* ; Drakos, E.* ; Beli, P.* ; Garinis, G.A.*

DNA damage in macrophages drives immune autoreactivity via nuclear antigen presentation.

Nature Aging 6, 393-413 (2026)
Verlagsversion Forschungsdaten DOI PMC
Open Access Hybrid
Creative Commons Lizenzvertrag
Aging and DNA damage increase the risk of chronic inflammation and autoimmunity, yet the molecular underpinnings remain unclear. In this study, we uncover a DNA damage-driven mechanism in macrophages that triggers immune autoreactivity. Here, using Er1Lyz2/- mice with a macrophage-specific DNA repair defect in ERCC1-XPF, we demonstrate that monocyte-derived macrophages accumulate DNA damage, activate the immune system, drive polyclonal T cell responses and generate antinuclear autoantibodies. Proteomic and immunopeptidomic analyses reveal a distinct major histocompatibility complex class II (MHC-II) antigen repertoire enriched in nuclear and ribosomal peptides, relying on autophagy for nuclear cargo delivery to MHC-II. Aged macrophages exhibit a similar lysosomal cargo profile, linking autophagy-driven nuclear antigen presentation to immune activation. Notably, inhibiting autophagy in Er1Lyz2/- mice suppresses autoimmune features, pinpointing autophagy-facilitated nuclear antigen processing as a central driver of age-related autoimmunity. These findings establish DNA damage-induced autophagy in macrophages as a pivotal mechanism linking aging to autoimmunity, unveiling potential therapeutic targets to mitigate age-related immune dysregulation.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Dna Damage ; Immune System ; Antigen Presentation ; Antigen ; Presentation (obstetrics) ; Dna; Class-ii Presentation; Mhc Class-i; Cockayne-syndrome; Aging Mice; T-cells; Autophagy; Repair; Activation; Stress; Consequences
ISSN (print) / ISBN 2662-8465
e-ISSN 2662-8465
Zeitschrift Nature Aging
Quellenangaben Band: 6, Heft: 2, Seiten: 393-413 Artikelnummer: , Supplement: ,
Verlag Springer
Verlagsort Campus, 4 Crinan St, London, N1 9xw, England
Begutachtungsstatus Peer reviewed
Institut(e) CF Metabolomics & Proteomics (CF-MPC)
Förderungen EC | Horizon 2020 Framework Programme (EU Framework Programme for Research and Innovation H2020)