The role of complement in antineutrophil cytoplasmic antibody-associated vasculitis.


Journal

Current opinion in rheumatology
ISSN: 1531-6963
Titre abrégé: Curr Opin Rheumatol
Pays: United States
ID NLM: 9000851

Informations de publication

Date de publication:
01 2019
Historique:
entrez: 22 11 2018
pubmed: 22 11 2018
medline: 16 1 2020
Statut: ppublish

Résumé

To provide a comprehensive overview of the current insight into the role of complement activation in antineutrophil cytoplasmic antibody-associated vasculitis (AAV). In addition, the therapeutic options targeting the complement system in AAV are discussed. It has become increasingly clear that complement, and more specifically signalling through the C5a receptor, contributes to the immunopathology of AAV. This has led to the design of clinical trials with a C5a receptor blocker. The first results show a reduction in tissue damage and a favourable safety profile, as other parts of the complement defence system are left intact. Although AAV was initially regarded as a pauci-immune disease, it is now well established that, in addition to autoantibodies, complement plays an essential role in the disease process. Animal models delivered the first insight, but the effective therapeutic interventions using complement inhibitors provided the proof that indeed complement activation contributes to disease activity and tissue damage in human AAV.

Identifiants

pubmed: 30461541
doi: 10.1097/BOR.0000000000000557
pii: 00002281-201901000-00003
doi:

Substances chimiques

Antibodies, Antineutrophil Cytoplasmic 0
Autoantibodies 0
Complement Inactivating Agents 0
Complement System Proteins 9007-36-7

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

3-8

Auteurs

Maria A C Wester Trejo (MAC)

Department of Pathology.

Leendert A Trouw (LA)

Department of Immunohematology and Blood Transfusion, Leiden University Medical Center, Leiden, the Netherlands.

Ingeborg M Bajema (IM)

Department of Pathology.

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Classifications MeSH