Ontology highlight
ABSTRACT: Objectives
To investigate the therapeutic potential of caspase-1 inhibition in systemic lupus erythematosus (SLE) and lupus nephritis (LN) using the MRL-Faslpr mouse model.Methods
Female Murphy Roths large (MRL)-Faslpr mice were treated with a caspase-1 inhibitor (pralnacase) or sham treatment from 2.5 to 5.5 months of age. Disease progression was assessed through analysis of systemic and renal parameters, including proteinuria, blood urea nitrogen, kidney histopathology and immune cell infiltration. Cytokine expression and caspase activity were measured to elucidate the mechanism of action. Additional experiments with interleukin (IL)-1 receptor antagonist and pancaspase inhibition treatment as well as post-disease onset intervention wer
SUBMITTER: Claßen P
PROVIDER: S-EPMC12730834 | biostudies-literature | 2025 Dec
REPOSITORIES: biostudies-literature