Anti-C1q in systemic lupus erythematosus

被引:34
|
作者
Stojan, G. [1 ]
Petri, M. [2 ]
机构
[1] Beth Israel Deaconess Med Ctr, Div Rheumatol, Boston, MA 02215 USA
[2] Johns Hopkins Univ, Div Rheumatol, Baltimore, MD USA
基金
美国国家卫生研究院;
关键词
Systemic lupus erythematosus; SLE; lupus nephritis; C1q; anti-C1q; COLLAGEN-LIKE REGION; IGG AUTOANTIBODIES; IMMUNE-COMPLEXES; PREDICTIVE-VALUE; ANTIBODIES; C1Q; NEPHRITIS; CLQ; IMMUNOLOGY; PREVALENCE;
D O I
10.1177/0961203316645205
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
C1q is the first component of the classical complement pathway. Both clinically validated in-house ELISA assays as well as commercial ELISA kits are used for detection of anti-C1q antibodies. Anti-C1q autoantibodies can be detected in a wide range of autoimmune diseases and are highly sensitive for hypocomplementemic uticarial vasculitis. In SLE, anti-C1q are strongly associated with proliferative lupus nephritis, and their absence carries a negative predictive value for development of lupus nephritis of close to 100%. Anti-C1q in combination with anti-dsDNA and low complement has the strongest serological association with renal involvement. The anti-C1q titers correlate with global disease activity scores in patients with renal involvement, and higher titers seem to precede renal flares. After the successful treatment of a renal flare, anti-C1q has the tendency to decrease or even become undetectable. The main obstacle to the inclusion of anti-C1q in the classification criteria and clinical management of SLE is the lack of standardized laboratory assays.
引用
收藏
页码:873 / 877
页数:5
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