Complement activation in IgA nephropathy

被引:84
作者
Medjeral-Thomas, Nicholas R. [1 ]
Cook, H. Terence [1 ]
Pickering, Matthew C. [1 ]
机构
[1] Imperial Coll London, Ctr Inflammatory Dis, Dept Immunol & Inflammat, London W12 0NN, England
基金
英国惠康基金;
关键词
Complement; IgA nephropathy; Immunology; Pathology; MANNAN-BINDING LECTIN; H-RELATED PROTEIN-5; GLOMERULAR DEPOSITION; PATHWAY; ECULIZUMAB; C3; SUSCEPTIBILITY; PATHOGENESIS; VARIANTS; INSIGHTS;
D O I
10.1007/s00281-021-00882-9
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
IgA nephropathy pathogenesis is incompletely understood, and this limits the development of disease-specific biomarkers and effective therapies. Evidence of complement activity in IgA nephropathy is well established. However, a growing body of research indicates complement activity is an important contributor to IgA nephropathy pathology. In particular, multiple associations have been identified between complement alternative, lectin and terminal pathway proteins and IgA nephropathy severity. Recently, we have also gained insight into possible mechanisms that could link glomerular IgA deposition, complement activity, glomerular inflammation and disease severity. Ongoing clinical trials of therapeutic complement inhibitors will provide insight into the importance of complement activity to IgA nephropathy pathogenesis. Further research into mechanisms of complement activity is essential to improving our understanding and management of patients with IgA nephropathy.
引用
收藏
页码:679 / 690
页数:12
相关论文
共 64 条
[1]   Individuals of Pacific Asian origin with IgA nephropathy have an increased risk of progression to end-stage renal disease [J].
Barbour, Sean J. ;
Cattran, Daniel C. ;
Kim, S. Joseph ;
Levin, Adeera ;
Wald, Ron ;
Hladunewich, Michelle A. ;
Reich, Heather N. .
KIDNEY INTERNATIONAL, 2013, 84 (05) :1017-1024
[2]   Update on C3 glomerulopathy [J].
Barbour, Thomas D. ;
Ruseva, Marieta M. ;
Pickering, Matthew C. .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2016, 31 (05) :717-725
[3]  
BERGER J, 1969, TRANSPL P, V1, P939
[4]  
Bruchfeld A, 2017, NEPHROL DIAL TRANSPL, V32
[5]   Plasma Galactose-Deficient IgA1 and C3 and CKD Progression in IgA Nephropathy [J].
Chen, Pei ;
Yu, Guizhen ;
Zhang, Xue ;
Xie, Xinfang ;
Wang, Jinwei ;
Shi, Sufang ;
Liu, Lijun ;
Lv, Jicheng ;
Zhang, Hong .
CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2019, 14 (10) :1458-1465
[6]   Complement-mediated microangiopathy in IgA nephropathy and IgA vasculitis with nephritis [J].
Chua, Jamie S. ;
Zandbergen, Malu ;
Wolterbeek, Ron ;
Baelde, Hans J. ;
van Es, Leendert A. ;
de Fijter, Johan W. ;
Bruijn, Jan A. ;
Bajema, Ingeborg M. .
MODERN PATHOLOGY, 2019, 32 (08) :1147-1157
[7]   Natural history of idiopathic IgA nephropathy and factors predictive of disease outcome [J].
D'Amico, G .
SEMINARS IN NEPHROLOGY, 2004, 24 (03) :179-196
[8]   Dimerization of complement factor H-related proteins modulates complement activation in vivo [J].
de Jorge, Elena Goicoechea ;
Caesar, Joseph J. E. ;
Malik, Talat H. ;
Patel, Mitali ;
Colledge, Matthew ;
Johnson, Steven ;
Hakobyan, Svetlana ;
Morgan, B. Paul ;
Harris, Claire L. ;
Pickering, Matthew C. ;
Lea, Susan M. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2013, 110 (12) :4685-4690
[9]   Biological variations of MASP-3 and MAp44, two splice products of the MASP1 gene involved in regulation of the complement system [J].
Degn, Soren E. ;
Jensen, Lisbeth ;
Gal, Peter ;
Dobo, Jozsef ;
Holmvad, Steffen H. ;
Jensenius, Jens C. ;
Thiel, Steffen .
JOURNAL OF IMMUNOLOGICAL METHODS, 2010, 361 (1-2) :37-50
[10]   The emerging roles of mannose-binding lectin-associated serine proteases (MASPs) in the lectin pathway of complement and beyond [J].
Dobo, Jozsef ;
Pal, Gabor ;
Cervenak, Laszlo ;
Gal, Peter .
IMMUNOLOGICAL REVIEWS, 2016, 274 (01) :98-111