Impact of MPO-ANCA-mediated oxidative imbalance on renal vasculitis

被引:9
作者
Hilhorst, Marc [1 ]
Maria, Alexandre T. J. [2 ,3 ]
Kavian, Niloufar [4 ,5 ]
Batteux, Frederic [4 ,5 ]
Borderie, Didier [6 ]
Le Quellec, Alain [2 ]
van Paassen, Pieter [1 ]
Guilpain, Philippe [2 ,3 ]
机构
[1] Maastricht Univ, Dept Clin & Expt Immunol, Maastricht, Netherlands
[2] Univ Hosp, Dept Internal Med & Multiorgan Dis, Montpellier, France
[3] INSERM, U1183, Inst Regenerat Med & Biotherapy, Montpellier, France
[4] INSERM, U1016, Inst Cochin, Fac Med Paris Descartes,Sorbonne Paris Cite, Paris, France
[5] Cochin Hosp, Lab Immunol, Paris, France
[6] Cochin Hosp, Lab Biochem, Paris, France
关键词
ANCA-associated vasculitis; glomerulonephritis; HOCl; microscopic polyangiitis; oxidative stress; thiol; ANTIMYELOPEROXIDASE ANTIBODIES; PROTEIN PRODUCTS; DISEASE; POLYANGIITIS; ANTIOXIDANT; FIBROSIS; RELAPSES; MARKER;
D O I
10.1152/ajprenal.00111.2018
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Glomerulonephritis is a severe complication of microscopic polyangiitis (MPA), a small-vessel vasculitis associated with anti-myeloperoxidase antibodies (MPO-ANCA). We previously showed the pathogenic effects of MPO-ANCA that activate MPO to trigger an oxidative burst mainly through HOCl production, contributing to endothelial injury and lung fibrosis. The aim of this study was to investigate the relationship between MPO-induced oxidative stress, anti-oxidant defenses and renal histological lesions in MPA patients. We therefore analyzed histological data from a prospective cohort of ANCA-associated glomerulonephritis. Serum-mediated HOCl production, advanced oxidation protein products (AOPP), and thiol concentration in sera were determined. From 38 patients included, histological classification noted 50% focal glomerulonephritis, 15.8% crescentic-glomerulonephritis, and 34.2% mixed-glomerulonephritis. MPA patients' sera displayed higher HOCl production by MPO (P < 0.001), higher AOPP (P < 0.001) and thiol (P < 0.01) levels, compared with healthy subjects. The presence of cellular crescents was associated with higher serum-mediated HOCl production (P = 0.049) and lower thiol levels (P = 0.022) at disease onset. Higher thiol concentrations were associated with focal glomerulonephritis (P = 0.042). less interstitial fibrosis (P = 0.039) and hyalinosis (P = 0.066). In remission, HOCl production was decreased (P < 0.01), and thiol concentration remained high (P = 0.39). Our findings suggest that HOCl production by activated MPO could contribute to the very early stage of glomerulonephritis, whereas thiol may exert a protective effect against the development of renal vasculitis and glomerulosclerosis. This study highlights the importance of oxidative defenses to counteract the process of MPO-ANCA associated glomerulonephritis.
引用
收藏
页码:F1769 / F1776
页数:8
相关论文
共 37 条
[1]  
Atalay M, 1996, EUR J APPL PHYSIOL O, V74, P342, DOI 10.1007/BF02226931
[2]   Histopathologic Classification of ANCA-Associated Glomerulonephritis [J].
Berden, Annelies E. ;
Ferrario, Franco ;
Hagen, E. Christiaan ;
Jayne, David R. ;
Jennette, J. Charles ;
Joh, Kensuke ;
Neumann, Irmgard ;
Noel, Laure-Helene ;
Pusey, Charles D. ;
Waldherr, Ruediger ;
Bruijn, Jan A. ;
Bajema, Ingeborg M. .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2010, 21 (10) :1628-1636
[3]  
BONSIB SM, 1985, AM J PATHOL, V119, P357
[4]   THE ROLE OF THIOL PROTEASES IN TISSUE-INJURY AND REMODELING [J].
CHAPMAN, HA ;
MUNGER, JS ;
SHI, GP .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1994, 150 (06) :S155-S159
[5]   Nrf2 defends the lung from oxidative stress [J].
Cho, HY ;
Reddy, SP ;
Kleeberger, SR .
ANTIOXIDANTS & REDOX SIGNALING, 2006, 8 (1-2) :76-87
[6]   Effect of Redox Modulating NRF2 Activators on Chronic Kidney Disease [J].
Choi, Bo-hyun ;
Kang, Kyung-Shin ;
Kwak, Mi-Kyoung .
MOLECULES, 2014, 19 (08) :12727-12759
[7]   CLINICAL COURSE OF ANTINEUTROPHIL CYTOPLASMIC AUTOANTIBODY-ASSOCIATED GLOMERULONEPHRITIS AND SYSTEMIC VASCULITIS [J].
FALK, RJ ;
HOGAN, S ;
CAREY, TS ;
JENNETTE, JC .
ANNALS OF INTERNAL MEDICINE, 1990, 113 (09) :656-663
[8]   DIFFERENCES BETWEEN ANTI-MYELOPEROXIDASE-3-ASSOCIATED AND ANTIPROTEINASE-3-ASSOCIATED RENAL-DISEASE [J].
FRANSSEN, CFM ;
GANS, ROB ;
ARENDS, B ;
HAGELUKEN, C ;
TERWEE, PM ;
GERLAG, PGG ;
HOORNTJE, SJ .
KIDNEY INTERNATIONAL, 1995, 47 (01) :193-199
[9]   The oxidation induced by antimyeloperoxidase antibodies triggers fibrosis in microscopic polyangiitis [J].
Guilpain, P. ;
Chereau, C. ;
Goulvestre, C. ;
Servettaz, A. ;
Montani, D. ;
Tamas, N. ;
Pagnoux, C. ;
Hachulla, E. ;
Weill, B. ;
Guillevin, L. ;
Mouthon, L. ;
Batteux, F. .
EUROPEAN RESPIRATORY JOURNAL, 2011, 37 (06) :1503-1513
[10]   Pathogenic effects of antimyeloperoxidase antibodies in patients with microscopic polyangiitis [J].
Guilpain, Philippe ;
Servettaz, Amelie ;
Goulvestre, Claire ;
Barrieu, Sandrine ;
Borderie, Didier ;
Chereau, Christiane ;
Kavian, Niloufar ;
Pagnoux, Christian ;
Guillevin, Loic ;
Weill, Bernard ;
Mouthon, Luc ;
Batteux, Frederic .
ARTHRITIS AND RHEUMATISM, 2007, 56 (07) :2455-2463