Our findings support a dual model of HS pathogenesis involving genetically driven epithelial dysfunction and systemic inflammation. The identification of HLA-DRA-associated variants raises the possibility that HS may share features with autoimmune diseases, while the proteomic profile dominated by innate cytokines suggests that an autoinflammatory component is also involved.
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M. Argyropoulou
National and Kapodistrian University of Athens
Georgios Tavoulareas
National and Kapodistrian University of Athens
Joyce Leman
Kings Park Hospital
Radboud University Nijmegen
University of Bonn
Radboud University Medical Center
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Argyropoulou et al. (Sat,) studied this question.
synapsesocial.com/papers/69ada8b2bc08abd80d5bbea3 — DOI: https://doi.org/10.1111/jdv.70390
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