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dc.contributor.author Rusai, Krisztina
dc.contributor.author Schmaderer C
dc.contributor.author Baumann M
dc.contributor.author Chmielewski S
dc.contributor.author Prókai, Ágnes
dc.contributor.author Kis, Éva PhD
dc.contributor.author Szabó, Attila
dc.contributor.author Leban J
dc.contributor.author Doblhofer R
dc.contributor.author Ammendola A
dc.contributor.author Lutz J
dc.contributor.author Heemann U
dc.date.accessioned 2016-06-06T12:39:54Z
dc.date.available 2016-06-06T12:39:54Z
dc.date.issued 2012
dc.identifier 84862299279
dc.identifier.citation pagination=1101-1107; journalVolume=93; journalIssueNumber=11; journalTitle=TRANSPLANTATION;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/2259
dc.identifier.uri doi:10.1097/TP.0b013e31824fd861
dc.description.abstract BACKGROUND: 4SC-101 is a novel dihydroorotate dehydrogenase inhibitor and a blocker of interleukin (IL)-17 secretion with beneficial effects in experimental lupus and inflammatory bowel disease. Its immunomodulatory effect on acute kidney rejection is not known; therefore, in this study, the impact of 4SC-101 was examined in a rat model of acute kidney rejection. METHODS: The kidneys of Brown-Norway rats were orthotopically transplanted into bilaterally nephrectomized Lewis recipients. Allograft recipients were administered with 4SC-101 at dosages of 4, 20, or 60 mg/kg per day, and survival was assessed. In the second setting, the animals were harvested 3 or 5 days after transplantation (Tx), and graft histologic diagnosis was determined. The effects of 4SC-101 on impaired renal function were examined in a model of 5/6 nephrectomy in Lewis rats. RESULTS: The recipients treated with 20-mg/kg 4SC-101 showed prolonged survival compared with placebo-treated animals (mean+/-SEM, 24+/-9.3 vs. 5.4+/-3 days), paralleled by less severe histologic features of acute kidney rejection such as interstitial/perivascular infiltration and tubulitis 3 and 5 days after Tx, and a lower level of IL-17 messenger RNA 5 days after Tx compared with the placebo-treated animals. In the 5/6 nephrectomy model, 20-mg/kg 4SC-101 reduced proteinuria, glomerulosclerosis, and fibrosis with decreased IL-17 messenger RNA expression. CONCLUSIONS: 4SC-101 prolongs survival after Tx, paralleled by amelioration of histologic signs of acute rejection. Furthermore, it showed no worsening effects on kidney function in a remnant kidney model and even slowed the progression of proteinuria and kidney fibrosis. Therefore, 4SC- 101 might be a promising pharmaceutical agent in Tx medicine for further investigations.
dc.relation.ispartof urn:issn:0041-1337
dc.title Immunosuppression With 4SC-101, a Novel Inhibitor of Dihydroorotate Dehydrogenase, in a Rat Model of Renal Transplantation
dc.type Journal Article
dc.date.updated 2015-11-03T11:20:39Z
dc.language.rfc3066 en
dc.identifier.mtmt 1973880
dc.identifier.wos 000305299000009
dc.identifier.pubmed 22609757
dc.contributor.department SE/AOK/K/I. Sz. Gyermekgyógyászati Klinika
dc.contributor.institution Semmelweis Egyetem


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