Immunological Pattern in IgA Nephropathy

被引:33
作者
Cols, Clara Esteve [1 ,2 ]
Graterol Torres, Freddzia-Amanda [3 ]
Quirant Sanchez, Bibiana [1 ,2 ]
Marco Rusinol, Helena [3 ]
Navarro Diaz, Maruja Isabel [3 ]
Ara del Rey, Jordi [3 ]
Martinez Caceres, Eva Ma [1 ,2 ]
机构
[1] Germans Trias & Pujol Univ Hosp & Res Inst, FOCIS Ctr Excellence UAB Barcelona, Immunol Div, LCMN, Badalona 08916, Spain
[2] Univ Autonoma Barcelona, Dept Cell Biol Physiol & Immunol, Bellaterra 08193, Spain
[3] Germans Trias & Pujol Univ Hosp, Nephrol Div, Badalona 08916, Spain
关键词
IgA Nephropathy; monocytes; CD89; biomarkers; OXFORD CLASSIFICATION; TRANSFERRIN RECEPTOR; MESANGIAL CELLS; PATHOGENESIS; GLYCOSYLATION; EXPRESSION; COMPLEXES; DISEASE; UPDATE;
D O I
10.3390/ijms21041389
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The current gold-standard diagnostic technique for IgA nephropathy (IgAN), the leading form of primary glomerulonephritis, is renal biopsy. CD89 (the main IgA receptor) is expressed on the surface of monocytes and plays a role in disease pathogenesis. Immunocomplexes formed by sCD89 (soluble form) and Gd-IgA1 are related to disease prognosis. We hypothesize that reduced CD89 surface expression on monocytes may be a marker of disease severity. We aimed to analyze leukocyte subpopulations in peripheral blood and CD89 surface expression on monocytes in a prospective study of 22 patients and 12 healthy subjects (HS). Leukocyte subpopulations and CD89 expression were analyzed by flow cytometry. IgAN patients had a higher percentage of activated and effector memory CD4(+) and CD8(+) T lymphocytes, a lower percentage of transitional B lymphocytes and plasmablasts, and a higher percentage of CD56(dim)CD16(+) NK cells and myeloid dendritic cells compared with HS. Correlations between reduced CD89 expression levels on nonclassical monocytes, histological findings of a poor prognosis on renal biopsy and baseline renal function were observed. IgAN patients show a characteristic immunological pattern in peripheral blood. A reduced expression level of CD89 on nonclassical monocytes identifies patients with a worse renal prognosis.
引用
收藏
页数:13
相关论文
共 33 条
[1]   IgA nephropathy [J].
Barratt, J ;
Feehally, J .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2005, 16 (07) :2088-2097
[2]   Recurrent IgA nephropathy is predicted by altered glycosylated IgA, autoantibodies and soluble CD89 complexes [J].
Berthelot, Laureline ;
Robert, Thomas ;
Vuiblet, Vincent ;
Tabary, Thierry ;
Braconnier, Antoine ;
Drame, Moustapha ;
Toupance, Olivier ;
Rieu, Philippe ;
Monteiro, Renato C. ;
Toure, Fatouma .
KIDNEY INTERNATIONAL, 2015, 88 (04) :815-822
[3]   Human dendritic cell functional specialization in steady-state and inflammation [J].
Boltjes, Arian ;
van Wijk, Femke .
FRONTIERS IN IMMUNOLOGY, 2014, 5
[4]   An update on the pathogenesis and treatment of IgA nephropathy [J].
Boyd, Joanna K. ;
Cheung, Chee K. ;
Molyneux, Karen ;
Feehally, John ;
Barratt, Jonathan .
KIDNEY INTERNATIONAL, 2012, 81 (09) :833-843
[5]   Phenotype, function, and differentiation potential of human monocyte subsets [J].
Boyette, Lisa B. ;
Macedo, Camila ;
Hadi, Kevin ;
Elinoff, Beth D. ;
Walters, John T. ;
Ramaswamil, Bala ;
Chalasani, Geetha ;
Taboas, Juan M. ;
Lakkis, Fadi G. ;
Metes, Diana M. .
PLOS ONE, 2017, 12 (04)
[6]   The Oxford classification of IgA nephropathy: rationale, clinicopathological correlations, and classification [J].
Cattran, Daniel C. ;
Coppo, Rosanna ;
Cook, H. Terence ;
Feehally, John ;
Roberts, Ian S. D. ;
Troyanov, Stephan ;
Alpers, Charles E. ;
Amore, Alessandro ;
Barratt, Jonathan ;
Berthoux, Francois ;
Bonsib, Stephen ;
Bruijn, Jan A. ;
D'Agati, Vivette ;
D'Amico, Giuseppe ;
Emancipator, Steven ;
Emma, Francesco ;
Ferrario, Franco ;
Fervenza, Fernando C. ;
Florquin, Sandrine ;
Fogo, Agnes ;
Geddes, Colin C. ;
Groene, Hermann-Josef ;
Haas, Mark ;
Herzenberg, Andrew M. ;
Hill, Prue A. ;
Hogg, Ronald J. ;
Hsu, Stephen I. ;
Jennette, J. Charles ;
Joh, Kensuke ;
Julian, Bruce A. ;
Kawamura, Tetsuya ;
Lai, Fernand M. ;
Leung, Chi Bon ;
Li, Lei-Shi ;
Li, Philip K. T. ;
Liu, Zhi-Hong ;
Mackinnon, Bruce ;
Mezzano, Sergio ;
Schena, F. Paolo ;
Tomino, Yasuhiko ;
Walker, Patrick D. ;
Wang, Haiyan ;
Weening, Jan J. ;
Yoshikawa, Nori ;
Zhang, Hong .
KIDNEY INTERNATIONAL, 2009, 76 (05) :534-545
[7]   The biology of human natural killer-cell subsets [J].
Cooper, MA ;
Fehniger, TA ;
Caligiuri, MA .
TRENDS IN IMMUNOLOGY, 2001, 22 (11) :633-640
[8]   Clinical and histological risk factors for progression of IgA nephropathy: an update in children, young and adult patients [J].
Coppo, Rosanna .
JOURNAL OF NEPHROLOGY, 2017, 30 (03) :339-346
[9]   Validation of the Oxford classification of IgA nephropathy in cohorts with different presentations and treatments [J].
Coppo, Rosanna ;
Troyanov, Stephan ;
Bellur, Shubha ;
Cattran, Daniel ;
Cook, H. Terence ;
Feehally, John ;
Roberts, Ian S. D. ;
Morando, Laura ;
Camilla, Roberta ;
Tesar, Vladimir ;
Lunberg, Sigrid ;
Gesualdo, Loreto ;
Emma, Francesco ;
Rollino, Cristiana ;
Amore, Alessandro ;
Praga, Manuel ;
Feriozzi, Sandro ;
Segoloni, Giuseppe ;
Pani, Antonello ;
Cancarini, Giovanni ;
Durlik, Magalena ;
Moggia, Elisabetta ;
Mazzucco, Gianna ;
Giannakakis, Costantinos ;
Honsova, Eva ;
Sundelin, B. Brigitta ;
Di Palma, Anna Maria ;
Ferrario, Franco ;
Gutierrez, Eduardo ;
Asunis, Anna Maria ;
Barratt, Jonathan ;
Tardanico, Regina ;
Perkowska-Ptasinska, Agnieszka .
KIDNEY INTERNATIONAL, 2014, 86 (04) :828-836
[10]   Altered monocyte expression and expansion of non-classical monocyte subset in IgA nephropathy patients [J].
Cox, Sharon N. ;
Serino, Grazia ;
Sallustio, Fabio ;
Blasi, Antonella ;
Rossini, Michele ;
Pesce, Francesco ;
Schena, Francesco Paolo .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2015, 30 (07) :1122-1132