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Republished: Antineutrophil cytoplasmic antibody-associated vasculitides: is it time to split up the group?
  1. Arnaud Millet1,2,3,4,
  2. Magali Pederzoli-Ribeil1,2,3,4,
  3. Loïc Guillevin5,
  4. Véronique Witko-Sarsat1,2,3,4,
  5. Luc Mouthon1,2,3,4
  1. 1INSERM U1016, Institut Cochin, Paris, France
  2. 2CNRS UMR 8104, Paris, France
  3. 3Université Paris-Descartes, Paris, France
  4. 4Laboratoire d'Excellence INFLAMEX Paris, France
  5. 5Hôpital Cochin, Assistance publique-Hôpitaux de Paris, service de médecine interne et centre de référence pour les vascularites nécrosantes et la sclérodermie systémique, Paris, France
  1. Correspondence to Dr Luc Mouthon, INSERM U1016, CNRS UMR 8104, 8 rue Mechain, Paris 75014, France; luc.mouthon{at}cch.aphp.fr

Abstract

Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitides are a heterogeneous group of diseases corresponding to necrotising inflammation of small vessels with a wide range of clinical presentations. At least two of the diseases are believed to exhibit a common ground of pathophysiological mechanisms. These are granulomatosis with polyangiitis (GPA, formerly known as Wegener's granulomatosis) and microscopic polyangiitis (MPA). ANCA directed against proteinase 3 (PR3) are preferentially associated with GPA, and anti-myeloperoxidase (MPO) ANCA are associated mainly with MPA and eosinophilic GPA (formerly known as Churg-Strauss syndrome). Anti-MPO and anti-PR3 antibodies can activate neutrophils in vitro. In vivo data are available for humans and mice on the pathogenicity of anti-MPO but it is more controversial for PR3-ANCA. A recent genome-wide association study of patients with ANCA-associated vasculitides confirmed the genetic contribution to the pathogenesis of these conditions, with significant association of PR3-ANCA and human leukocyte antigen-DP and the genes encoding α1-antitrypsin and PR3. MPO-ANCA were significantly associated with human leukocyte antigen-DQ. Thus, recent results from epidemiological studies, genome-wide association study and therapeutic trials have suggested that these entities are, in fact, distinct. We have summarised these results and discuss the idea that these two entities should be studied separately as the nature of the two auto-antigens suggests at a molecular level despite shared ANCA involvement.

  • Autoantibodies
  • Granulomatosis with polyangiitis
  • Inflammation

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