Literature DB >> 11576349

LF15-0195 prevents the induction and inhibits the progression of rat anti-GBM disease.

G H Tesch1, P A Hill, M Wei, D J Nikolic-Paterson, P Dutartre, R C Atkins.   

Abstract

BACKGROUND: LF15-0195 is a novel immunosuppressant that is currently in phase II clinical trials for the treatment of vasculitis. This study examined whether LF15-0195 could suppress the induction and progression of rat anti-glomerular basement membrane (anti-GBM) glomerulonephritis.
METHODS: Rapidly progressive glomerulonephritis was induced in primed rats by the administration of anti-GBM serum. In the first experiment, LF15-0195 was given daily by subcutaneous injection (days 0 to 14) to treat the induction of anti-GBM disease analyzed at day 14. In a second experiment, rats received LF15-0195 as an intervention treatment from days 7 to 28 (continuous therapy) or days 7 to 12 (pulse therapy) to treat the progression of disease assessed at day 28.
RESULTS: Continuous LF15-0195 treatment during the induction of anti-GBM disease (experiment 1) prevented proteinuria and loss of renal function, and markedly reduced histological kidney lesions and renal fibrosis. LF15-0195 also reduced kidney leukocyte infiltrate, urine excretion of interleukin-1beta (IL-1beta) and transforming growth factor-beta (TGF-beta), and the serum antibody response, but not kidney deposition of Ig and C3. When LF15-0195 treatment was initiated at day 7, both continuous and pulse therapy partially inhibited disease progression by suppressing the loss of renal function, interstitial macrophage and T-cell accumulation, tubular cell proliferation, and renal fibrosis.
CONCLUSION: LF15-0195 prevents the induction and suppresses the progression of rat anti-GBM disease through multiple mechanisms of action, suggesting that this drug may have significant therapeutic potential in human glomerulonephritis. The similar efficacy of continuous and pulse intervention treatment in this model indicates that short-term LF15-0195 treatment may achieve optimal benefit without prolonged bone marrow suppression.

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Year:  2001        PMID: 11576349     DOI: 10.1046/j.1523-1755.2001.00940.x

Source DB:  PubMed          Journal:  Kidney Int        ISSN: 0085-2538            Impact factor:   10.612


  4 in total

1.  Myeloid mineralocorticoid receptor activation contributes to progressive kidney disease.

Authors:  Louis L Huang; David J Nikolic-Paterson; Yingjie Han; Elyce Ozols; Frank Y Ma; Morag J Young; Greg H Tesch
Journal:  J Am Soc Nephrol       Date:  2014-04-03       Impact factor: 10.121

2.  Induction of T regulatory cells attenuates idiopathic nephrotic syndrome.

Authors:  Ludmilla Le Berre; Sarah Bruneau; Jeanne Naulet; Karine Renaudin; Françoise Buzelin; Claire Usal; Helga Smit; Thomas Condamine; Jean-Paul Soulillou; Jacques Dantal
Journal:  J Am Soc Nephrol       Date:  2008-11-19       Impact factor: 10.121

3.  Is there B cell involvement in a rat model of spontaneous idiopathic nephrotic syndrome treated with LF15-0195?

Authors:  Ludmilla Le Berre; Gaëlle Tilly; Jacques Dantal
Journal:  J Nephrol       Date:  2014-03-25       Impact factor: 3.902

Review 4.  Targeting the Monocyte-Macrophage Lineage in Solid Organ Transplantation.

Authors:  Thierry P P van den Bosch; Nynke M Kannegieter; Dennis A Hesselink; Carla C Baan; Ajda T Rowshani
Journal:  Front Immunol       Date:  2017-02-16       Impact factor: 7.561

  4 in total

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