TY - JOUR
T1 - The Complement System and ANCA Associated Vasculitis in the Era of Anti-Complement Drugs
AU - Kimoto, Yasutaka
AU - Horiuchi, Takahiko
N1 - Funding Information:
TH reports grants from the Ministry of Health, Labour and Welfare (MHLW) (H29-013), Japan, grants from the Ministry of Education, Culture, Sports, Science, and Technology (MEXT)(16K09246, 19H03564), Japan.
Publisher Copyright:
Copyright © 2022 Kimoto and Horiuchi.
PY - 2022/6/23
Y1 - 2022/6/23
N2 - 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.
AB - 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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U2 - 10.3389/fimmu.2022.926044
DO - 10.3389/fimmu.2022.926044
M3 - Review article
C2 - 35812453
AN - SCOPUS:85133871962
SN - 1664-3224
VL - 13
JO - Frontiers in Immunology
JF - Frontiers in Immunology
M1 - 926044
ER -