Frontiers in Immunology (Nov 2023)

ANCA-negative EGPA: only eosinophils without vasculitis? Insights from anti-T2 biologics

  • Mario Andrea Piga,
  • Paolo Fraticelli,
  • Leonardo Antonicelli,
  • Maria Stella Garritani,
  • Giulia Ghirelli,
  • Matteo Martini,
  • Matteo Martini,
  • Angelica Di Vincenzo,
  • Angelica Di Vincenzo,
  • Maria Giovanna Danieli,
  • Maria Giovanna Danieli,
  • Maria Giovanna Danieli,
  • Gianluca Moroncini,
  • Gianluca Moroncini,
  • Gianluca Moroncini,
  • Gianluca Moroncini,
  • Maria Beatrice Bilò,
  • Maria Beatrice Bilò,
  • Maria Beatrice Bilò

DOI
https://doi.org/10.3389/fimmu.2023.1325299
Journal volume & issue
Vol. 14

Abstract

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The pathogenic role of p-ANCA in eosinophilic granulomatosis with polyangiitis (EGPA) is a long-standing matter of debate. In this work, we report our real-life experience with EGPA patients, treated with biologics targeting type 2 (T2)-eosinophilic inflammation (Mepolizumab, Benralizumab, Dupilumab). Interestingly, we observed EGPA extrarespiratory relapses only in p-ANCA-positive patients (2/5 cutaneous vasculitis, 3/5 constitutional symptoms), with new rise of p-ANCA and normal eosinophil blood count. Notably, revising our cohort with the new ACR 2022 criteria, these five patients were the only ones to satisfy the entry criterion of vasculitis’ defined diagnosis at disease onset. These observations may suggest that biologics, selectively turning off T2 inflammation, may have unmasked p-ANCA exclusive role in the pathogenesis of vasculitis in EGPA. Therefore, we raise the question whether EGPA vasculitis exists only in p-ANCA-positive patients, and whether p-ANCA-negative disease is “only eosinophils without vasculitis”.

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