Literature DB >> 15213264

Experimental autoimmune anti-glomerular basement membrane glomerulonephritis: a protective role for IFN-gamma.

A Richard Kitching1, Amanda L Turner, Timothy Semple, Ming Li, Kristy L Edgtton, Gabrielle R Wilson, Jennifer R Timoshanko, Billy G Hudson, Stephen R Holdsworth.   

Abstract

IL-12 and IFN-gamma play key roles in murine lupus and planted antigen models of glomerulonephritis. However, their roles in renal organ-specific autoimmunity are unknown. To establish the roles of endogenous IFN-gamma and IL-12 in experimental autoimmune anti-glomerular basement membrane (GBM) glomerulonephritis (EAG), EAG was induced in normal C57BL/6 mice (WT), IL-12p40-deficient (IL-12p40-/-) mice, and IFN-gamma-deficient (IFN-gamma-/-) mice by immunization with alpha3-alpha5(IV)NC1 heterodimers. At 13 wk, WT mice developed EAG with linear mouse anti-GBM antibody deposition, histologic injury, proteinuria, and mild tubulointerstitial disease. Compared with WT mice, IL-12p40-/- mice had decreased histologic injury and trends to decreased leukocyte infiltrates. In contrast, 40% (4 of 10) of IFN-gamma-/- mice developed significant crescent formation and focal or diffuse interstitial infiltrates (WT, 0 of 8). Compared with WT and/or IL-12p40-/- mice, IFN-gamma-/- mice developed increased injury: histologic injury, total glomerular cell numbers, leukocytes in glomeruli, and renal expression of P-selectin and intercellular adhesion molecule 1. All groups developed similar serum anti-alpha3-alpha5(IV)NC1 antibodies and glomerular Ig deposition, but IFN-gamma-/- mice had decreased anti-alpha3-alpha5(IV)NC1 IgG2a. Therefore, IFN-gamma-/- mice developed increased cellular reactants despite a potentially less damaging antibody response. Dermal delayed-type hypersensitivity was increased in alpha3-alpha5(IV)NC1 immunized IFN-gamma-/- mice and was suppressed by recombinant murine IFN-gamma. CD4+ cells from draining nodes of immunized IFN-gamma-/- mice showed increased proportions of proliferating CD4+ cells but similar numbers of apoptotic cells. These studies demonstrate that in renal organ-specific autoimmunity, IL-12 is pathogenetic but IFN-gamma is protective. They lend weight to the hypothesis that depending on the context/severity of the nephritogenic immune response IFN-gamma has different effects.

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Year:  2004        PMID: 15213264     DOI: 10.1097/01.asn.0000128968.27705.5e

Source DB:  PubMed          Journal:  J Am Soc Nephrol        ISSN: 1046-6673            Impact factor:   10.121


  24 in total

Review 1.  Role of T cells and dendritic cells in glomerular immunopathology.

Authors:  Christian Kurts; Felix Heymann; Veronika Lukacs-Kornek; Peter Boor; Jürgen Floege
Journal:  Semin Immunopathol       Date:  2007-10-23       Impact factor: 9.623

Review 2.  The role of necrotic cell death in the pathogenesis of immune mediated nephropathies.

Authors:  Neelakshi R Jog; Roberto Caricchio
Journal:  Clin Immunol       Date:  2014-05-17       Impact factor: 3.969

3.  Alport alloantibodies but not Goodpasture autoantibodies induce murine glomerulonephritis: protection by quinary crosslinks locking cryptic α3(IV) collagen autoepitopes in vivo.

Authors:  Wentian Luo; Xu-Ping Wang; Clifford E Kashtan; Dorin-Bogdan Borza
Journal:  J Immunol       Date:  2010-08-13       Impact factor: 5.422

4.  Granulomatous transformation of capillary lesions in pulmonary-renal syndrome autologously induced anti-glomerular basement membrane disease in Wistar-Kyoto rats.

Authors:  Daiju Aoyagi; Koh Nakazawa; Tomoki Kaneyama; Junya Masumoto; Masako Otani; Hidekazu Shigematsu
Journal:  Clin Exp Nephrol       Date:  2010-01-09       Impact factor: 2.801

5.  IL-23, not IL-12, directs autoimmunity to the Goodpasture antigen.

Authors:  Joshua D Ooi; Richard K S Phoon; Stephen R Holdsworth; A Richard Kitching
Journal:  J Am Soc Nephrol       Date:  2009-04-08       Impact factor: 10.121

6.  Serum-starved adipose-derived stromal cells ameliorate crescentic GN by promoting immunoregulatory macrophages.

Authors:  Kazuhiro Furuhashi; Naotake Tsuboi; Asuka Shimizu; Takayuki Katsuno; Hangsoo Kim; Yosuke Saka; Takenori Ozaki; Yoshikazu Sado; Enyu Imai; Seiichi Matsuo; Shoichi Maruyama
Journal:  J Am Soc Nephrol       Date:  2013-03-07       Impact factor: 10.121

7.  Renal dendritic cells stimulate IL-10 production and attenuate nephrotoxic nephritis.

Authors:  Juliane Scholz; Veronika Lukacs-Kornek; Daniel R Engel; Sabine Specht; Eva Kiss; Frank Eitner; Jürgen Floege; Herrmann-Josef Groene; Christian Kurts
Journal:  J Am Soc Nephrol       Date:  2008-01-30       Impact factor: 10.121

8.  Th1 and Th17 cells induce proliferative glomerulonephritis.

Authors:  Shaun A Summers; Oliver M Steinmetz; Ming Li; Joshua Y Kausman; Timothy Semple; Kristy L Edgtton; Dorin-Bogdan Borza; Hal Braley; Stephen R Holdsworth; A Richard Kitching
Journal:  J Am Soc Nephrol       Date:  2009-10-09       Impact factor: 10.121

9.  Suppression of experimental autoimmune glomerulonephritis by tryptophan.

Authors:  Weiping Hou; Gang Huang; Xuejiao Cao; Yuanyuan Zhang; Jinbo Zhang; Yan Li
Journal:  J Nephrol       Date:  2013-12-13       Impact factor: 3.902

10.  Cross-reactive myelin antibody induces renal pathology.

Authors:  Lisa K Peterson; Takahisa Masaki; Steven R Wheelwright; Ikuo Tsunoda; Robert S Fujinami
Journal:  Autoimmunity       Date:  2008-11       Impact factor: 2.815

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