Poly-IgA Complexes and Disease Severity in IgA Nephropathy

被引:17
|
作者
Zhang, Xue [1 ,2 ,3 ,4 ,5 ,6 ]
Lv, Jicheng [1 ,2 ,3 ,4 ,5 ,6 ]
Liu, Pan [7 ,8 ]
Xie, Xinfang [7 ,8 ]
Wang, Manliu [1 ,2 ,3 ,4 ,5 ,6 ]
Liu, Dan [9 ]
Zhang, Hong [1 ,2 ,3 ,4 ,5 ,6 ]
Jin, Jing [7 ,8 ]
机构
[1] Peking Univ First Hosp, Renal Div, 8 Xishiku St, Beijing 100034, Peoples R China
[2] Peking Univ, Inst Nephrol, Beijing, Peoples R China
[3] Minist Hlth China, Key Lab Renal Dis, Beijing, Peoples R China
[4] Peking Univ, Key Lab Chron Kidney Dis Prevent & Treatment, Minist Educ, Beijing, Peoples R China
[5] Chinese Acad Med Sci, Res Unit Diag, Beijing, Peoples R China
[6] Chinese Acad Med Sci, Res Unit Treatment Immune Mediated Kidney Dis, Beijing, Peoples R China
[7] Northwestern Univ, Feinberg Sch Med, Div Nephrol, Chicago, IL 60611 USA
[8] Northwestern Univ, Feinberg Sch Med, Feinberg Cardiovasc & Renal Res Inst, Chicago, IL 60611 USA
[9] Peking Univ, Med & Hlth Analyt Ctr, Prote Lab, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
IgA nephropathy; glomerulonephritis; immune complexes; Fc receptors; FC-ALPHA-RI; CIRCULATING IMMUNE-COMPLEXES; IMMUNOGLOBULIN-A; RECEPTOR CD89; MESANGIAL CELLS; HINGE-REGION; SERUM IGA; BINDING; JACALIN; FC-ALPHA-RI/CD89;
D O I
10.2215/CJN.01300121
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
Background and objectives Poly-IgA immune complex formation and glomerular deposition play a key role in IgA nephropathy. Our study sought to develop a new methodology for one-step serologic detection of poly-IgA levels. Design, setting, participants, & measurements A novel ELISA method using recombinant CD89 as a ?capturing? probe was established for detecting poly-IgA immune complex in plasma. We applied semiquantitative measurements of these poly-IgA indices in patients recruited at Peking University First Hospital who had IgA nephropathy or other kidney disease types, as compared with healthy controls. The longitudinal trend of the poly-IgA index and the association with pathologic parameters and treatment responses were evaluated. Finally, we analyzed the molecular composition of poly-IgA complexes in patients by mass spectrometry. Results Recombinant CD89?mounted ELISA plates specifically captured plasma poly-IgA. The levels of poly-IgA immune complex (26.7 [interquartile range (IQR) 17.1?42.6] U/ml) in IgA nephropathy were significantly higher than those in healthy controls (15.5 [IQR 10.7?20.0] U/ml; P<0.001) or in controls with non-IgA nephropathy disease (14.8 [IQR 10.5?21.9] U/ml; P<0.001). Higher levels of poly-IgA immune complex were associated with lower eGFR and worse kidney outcome. Accuracy parameters and concordant statistics showed good discrimination between IgA nephropathy and healthy controls based on poly-IgA index levels (area under the curve [AUC], 0.78; 95% confidence interval [95% CI], 0.72 to 0.83; P<0.001), significantly outperforming galactose-deficient IgA1 levels (AUC, 0.70; P=0.05). Corticosteroid and immunosuppressant treatments lowered poly-IgA indices. After a recombinant CD89?directed workflow in conjunction with mass spectrometry, we also analyzed the molecular composition of IgA immune complex in patients with IgA nephropathy. Conclusions Higher level of recombinant CD89?bound poly-IgA immune complex was associated with the severity of the disease and with treatment response to steroids and immunosuppressants.
引用
收藏
页码:1652 / 1664
页数:13
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