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J Leukoc Biol. 2017 Sep;102(3):689-698. doi: 10.1189/jlb.3MR0217-069R. Epub 2017 May 25.

Proteinase 3: the odd one out that became an autoantigen.

Martin KR1,2,3,4, Witko-Sarsat V5,2,3,4.

Author information

1
Institut National de la Santé et de la Recherche Médicale, U1016, Institut Cochin, Paris, France.
2
Centre National de la Recherche Scientifique-Unité Mixte de Recherche 8104, Paris, France.
3
Université Paris Descartes, Sorbonne Paris Cité, Paris, France; and.
4
Center of Excellence, LabEx Inflamex, Paris, France.
5
Institut National de la Santé et de la Recherche Médicale, U1016, Institut Cochin, Paris, France; veronique.witko@inserm.fr.

Abstract

Neutrophils are critical in the defense against bacterial and fungal pathogens, and they also modulate the inflammatory process. The areas where neutrophils are studied have expanded from the restricted field of antibacterial defense to the modulation of inflammation and finally, to fine-tuning immune responses. As a result, recent studies have shown that neutrophils are implicated in several systemic autoimmune diseases, although exactly how neutrophils contribute to these diseases and the molecular mechanisms responsible are still under investigation. In a group of autoimmune vasculitides associated with anti-neutrophil cytoplasmic antibodies (AAVs), granulomatosis with polyangiitis (GPA) illustrates the concept that autoimmunity can develop against one specific neutrophil protein, namely, proteinase 3 (PR3), one of the four serine protease homologs contained within azurophilic granules. In this review, we will focus on recent molecular analyses combined with functional studies that provide clear evidence that the pathogenic properties of PR3 are not only a result of its enzymatic activity but also mediated by a particular structural element-the hydrophobic patch-which facilitates associations with various proteins and lipids and permits anchorage into the plasma membrane. Furthermore, these unique structural and functional characteristics of PR3 might be key contributors to the systemic inflammation and to the immune dysregulation observed in GPA.

KEYWORDS:

ANCA-associated vasculitis; granulomatosis with polyangiitis; myeloblastin; neutrophil elastase; neutrophils

PMID:
28546501
DOI:
10.1189/jlb.3MR0217-069R
[Indexed for MEDLINE]

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