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    Strain differences and the genetic basis of experimental autoimmune anti-glomerular basement membrane glomerulonephritis.

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    Authors
    Reynolds, John
    Affiliation
    University of Bedfordshire
    Issue Date
    2011-06
    
    Metadata
    Show full item record
    Abstract
    Goodpasture's, or anti-glomerular basement membrane (GBM), disease presents with rapidly progressive glomerulonephritis, caused by autoimmunity to a component of the GBM, the non-collagenous domain of the α3 chain of type IV collagen [α3(IV)NC1]. To investigate the mechanisms of inflammation in glomerulonephritis and to test new approaches to treatment, animal models of glomerulonephritis, termed experimental autoimmune glomerulonephritis (EAG), have been developed in susceptible strains of rats and mice. This review article describes how these models of EAG have been developed over the past three decades, discusses the evidence for the involvement of both humoral and cell-mediated immunity in the induction and pathogenesis of glomerulonephritis in these models and highlights recent, emerging data that have identified potential candidate genes that may control the genetic susceptibility in these different strains of rats and mice. The identification of these susceptibility genes has lead to a better understanding of the genetic basis of this model of anti-GBM disease, which may be relevant to the immunopathogenesis of Goodpasture's disease, and more generally to the progression from autoimmunity to target-organ damage.
    Citation
    Reynolds, J. (V) 'Strain differences and the genetic basis of experimental autoimmune anti-glomerular basement membrane glomerulonephritis' International journal of experimental pathology, 92 (3):211-217 Int J Exp Pathol
    Publisher
    Blackwell Publishing
    Journal
    International journal of experimental pathology
    URI
    http://hdl.handle.net/10547/228739
    DOI
    10.1111/j.1365-2613.2011.00763.x
    PubMed ID
    21342299
    Additional Links
    https://onlinelibrary.wiley.com/doi/abs/10.1111/j.1365-2613.2011.00763.x
    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3101493/
    Type
    Article
    Language
    en
    ISSN
    1365-2613
    ae974a485f413a2113503eed53cd6c53
    10.1111/j.1365-2613.2011.00763.x
    Scopus Count
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