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Complement in antineutrophil cytoplasmic antibody-associated vasculitis
被引:3
作者:
Yuan, Jun
[1
,2
,3
,4
,5
,6
,7
]
Chen, Min
[1
,2
,3
,4
,5
]
Zhao, Ming-Hui
[1
,2
,3
,4
,5
]
机构:
[1] Peking Univ, Hosp 1, Dept Med, Div Renal, Beijing 100034, Peoples R China
[2] Peking Univ, Inst Nephrol, Beijing 100034, Peoples R China
[3] Minist Hlth China, Key Lab Renal Dis, Beijing 100034, Peoples R China
[4] Minist Educ China, Key Lab CKD Prevent & Treatment, Beijing 100034, Peoples R China
[5] Peking Tsinghua Ctr Life Sci, Beijing 100034, Peoples R China
[6] Hubei Univ Tradit Chinese Med, Wuhan 430061, Peoples R China
[7] Hubei Hosp Tradit Chinese Med, Wuhan 430061, Peoples R China
关键词:
ANCA;
Vasculitis;
Complement;
ACTIVATION;
GLOMERULONEPHRITIS;
AUTOANTIBODIES;
NEUTROPHILS;
PATHOGENESIS;
RECEPTORS;
MICE;
C5A;
D O I:
10.1007/s10157-012-0700-9
中图分类号:
R5 [内科学];
R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号:
1002 ;
100201 ;
摘要:
Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis is a group of autoimmune disorders. It was previously assumed that the complement system is not involved in the development of ANCA-associated vasculitis due to its "pauci-immune" feature in renal histology. However, increasing evidence indicates that activation of the complement system, especially via the alternative complement pathway, plays a crucial role in the pathogenesis of ANCA-associated vasculitis. In this brief review, we discuss the evidence, including in vivo, in vitro, and clinical studies, for complement system activation in ANCA-associated vasculitis.
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页码:642 / 645
页数:4
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