Interleukin 6 (IL-6) deficiency delays lupus nephritis in MRL-Faslpr mice: the IL-6 pathway as a new therapeutic target in treatment of autoimmune kidney disease in …

H Cash, M Relle, J Menke, C Brochhausen… - The Journal of …, 2010 - jrheum.org
Objective. To investigate the pathophysiological effect of interleukin 6 (IL-6) on lupus nephritis
in MRL-Fas lpr mice. Methods. We generated IL-6-deficient MRL-Fas lpr mice using a …

Genetics and novel aspects of therapies in systemic lupus erythematosus

M Relle, J Weinmann-Menke, E Scorletti, L Cavagna… - Autoimmunity …, 2015 - Elsevier
… Author links open overlay panel Manfred Relle a 1 , Julia Weinmann-Menke a 1 , Eva
Scorletti b , Lorenzo Cavagna b 2 , Andreas Schwarting a c 2 …

[HTML][HTML] Role of MHC-linked susceptibility genes in the pathogenesis of human and murine lupus

M Relle, A Schwarting - Journal of Immunology Research, 2012 - hindawi.com
Systemic lupus erythematosus (SLE) is a chronic autoimmune disease characterized by the
production of autoantibodies against nuclear antigens and a systemic inflammation that can …

[HTML][HTML] Targeting transcription factor Stat4 uncovers a role for interleukin-18 in the pathogenesis of severe lupus nephritis in mice

…, T Bork, B Kutska, KT Byrne, M Blanfeld, M Relle… - Kidney international, 2011 - Elsevier
Polymorphisms in the transcription factor Stat4 gene have been implicated as risk factors for
systemic lupus erythematosus. Although some polymorphisms have a strong association …

Interferon-β: A Therapeutic for Autoimmune Lupus in MRL-: Faslpr: Mice

…, T Hansen, W Brenner, VR Kelley, M Relle… - Journal of the …, 2005 - journals.lww.com
Type I interferons are associated with lupus. Genes that are regulated by IFN-α are upregulated
in pediatric lupus patients. Gene deletion of the IFN-α/β receptor in experimental lupus-…

Mast Cell–deficient KitW-sh “Sash” Mutant Mice Display Aberrant Myelopoiesis Leading to the Accumulation of Splenocytes That Act as Myeloid-Derived Suppressor …

…, T Bopp, M Radsak, M Hoffmann, M Relle… - The Journal of …, 2013 - journals.aai.org
Mast cell-deficient Kit W-sh “sash” mice are widely used to investigate mast cell functions.
However, mutations of c-Kit also affect additional cells of hematopoietic and nonimmune origin…

[HTML][HTML] New perspectives on the renal slit diaphragm protein podocin

M Relle, H Cash, C Brochhausen, D Strand… - Modern …, 2011 - nature.com
Podocin is a critical component of the glomerular filtration barrier, its mutations causing
recessive steroid-resistant nephrotic syndrome. A GenBank analysis of the human podocin (…

Genetics and pathophysiology of granulomatosis with polyangiitis (GPA) and its main autoantigen proteinase 3

M Relle, B Föhr, F Fasola, A Schwarting - Molecular and cellular probes, 2016 - Elsevier
Granulomatosis with polyangiitis (GPA) is a severe autoimmune disease and one of the small
vessel anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitides. Although its …

Mast cell-derived mediators promote murine neutrophil effector functions

…, S Reuter, P Friedrich, L Böhm, M Relle… - International …, 2013 - academic.oup.com
Mast cells are able to trigger life-saving immune responses in murine models for acute
inflammation. In such settings, several lines of evidence indicate that the rapid and protective …

[HTML][HTML] Downregulation of α-galactosidase A upregulates CD77: Functional impact for Fabry nephropathy

T Thomaidis, M Relle, M Golbas, C Brochhausen… - Kidney international, 2009 - Elsevier
Anderson–Fabry disease, an inherited deficiency in the lysosomal enzyme α-galactosidase
A, is characterized by the progressive accumulation of globotriaosylceramide (Gb3), also …