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The Complement System and ANCA Associated Vasculitis in the Era of Anti-Complement Drugs

ANCA (anti-neutrophil cytoplasmic antibody)-associated vasculitis (AAV) is the condition in which ANCA, as an autoantibody, is associated with the pathogenesis of vasculitis in small blood vessels, mainly in the ear, nose, throat, kidney, lung, and nerves. These diseases are important because they c...

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Autores principales: Kimoto, Yasutaka, Horiuchi, Takahiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9260009/
https://www.ncbi.nlm.nih.gov/pubmed/35812453
http://dx.doi.org/10.3389/fimmu.2022.926044
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author Kimoto, Yasutaka
Horiuchi, Takahiko
author_facet Kimoto, Yasutaka
Horiuchi, Takahiko
author_sort Kimoto, Yasutaka
collection PubMed
description ANCA (anti-neutrophil cytoplasmic antibody)-associated vasculitis (AAV) is the condition in which ANCA, as an autoantibody, is associated with the pathogenesis of vasculitis in small blood vessels, mainly in the ear, nose, throat, kidney, lung, and nerves. These diseases are important because they can be fatal due to renal failure and pulmonary hemorrhage if not promptly and appropriately treated. Recently accumulated evidence has shown that C5a produced by the complement alternative pathway primes neutrophils, which in turn activate the complement alternative pathway, leading to the pathogenesis of AAV. Avacopan (CCX168), a C5aR antagonist was shown to be effective against AAV, and it has been a novel therapeutic option, becoming a novel anti-complement drug to modulate inflammatory diseases.
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spelling pubmed-92600092022-07-08 The Complement System and ANCA Associated Vasculitis in the Era of Anti-Complement Drugs Kimoto, Yasutaka Horiuchi, Takahiko Front Immunol Immunology ANCA (anti-neutrophil cytoplasmic antibody)-associated vasculitis (AAV) is the condition in which ANCA, as an autoantibody, is associated with the pathogenesis of vasculitis in small blood vessels, mainly in the ear, nose, throat, kidney, lung, and nerves. These diseases are important because they can be fatal due to renal failure and pulmonary hemorrhage if not promptly and appropriately treated. Recently accumulated evidence has shown that C5a produced by the complement alternative pathway primes neutrophils, which in turn activate the complement alternative pathway, leading to the pathogenesis of AAV. Avacopan (CCX168), a C5aR antagonist was shown to be effective against AAV, and it has been a novel therapeutic option, becoming a novel anti-complement drug to modulate inflammatory diseases. Frontiers Media S.A. 2022-06-23 /pmc/articles/PMC9260009/ /pubmed/35812453 http://dx.doi.org/10.3389/fimmu.2022.926044 Text en Copyright © 2022 Kimoto and Horiuchi https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Kimoto, Yasutaka
Horiuchi, Takahiko
The Complement System and ANCA Associated Vasculitis in the Era of Anti-Complement Drugs
title The Complement System and ANCA Associated Vasculitis in the Era of Anti-Complement Drugs
title_full The Complement System and ANCA Associated Vasculitis in the Era of Anti-Complement Drugs
title_fullStr The Complement System and ANCA Associated Vasculitis in the Era of Anti-Complement Drugs
title_full_unstemmed The Complement System and ANCA Associated Vasculitis in the Era of Anti-Complement Drugs
title_short The Complement System and ANCA Associated Vasculitis in the Era of Anti-Complement Drugs
title_sort complement system and anca associated vasculitis in the era of anti-complement drugs
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9260009/
https://www.ncbi.nlm.nih.gov/pubmed/35812453
http://dx.doi.org/10.3389/fimmu.2022.926044
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