Inflammation and Autoimmunity

Systemic Lupus Erythematosus

Biocytogen has developed Pristane-induced SLE mouse models and MRL/lpr spontaneous SLE mouse models for pharmacological and efficacy evaluation of SLE therapeutics. In addtion, we have generated over 900 human target KI mice covering SLE related targets for testing various drugs.

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  • SLE Mouse Model Introduction
  • Results

Publication

    SLE Mouse Model Introduction

    Systemic lupus erythematosus (SLE) is a severe autoimmune disease characterized by dysfunction of immune regulation, overproduction of inflammatory cytokines and attack on normal tissues (heart, joints, skin, lungs, blood vessels, liver, kidneys, and the nervous system) by self-reactive cells and antibodies.

    Pristane, also known as hydrocarbon oil (2,6,10,14- tetramethylpentadecane, TMPD), is capable of triggering a wide range of autoantibodies. Mice receive priatane develop an ascitic fluid enriched with monoclonal antibodies, local chronic inflammation (lipogranulomas), and a rheumatoid-like erosive arthritis. These clinical manifestations resemble SLE.

    Biocytogen has developed Pristane-induced SLE mouse models and MRL/lpr spontaneous SLE mouse models for pharmacological and efficacy evaluation of SLE therapeutics. In addtion, we have generated over 900 human target KI mice covering SLE related targets for testing various drugs.

    Results
    Pristane-induced Systemic Lupus Erythematosus (SLE) Mouse Model
    Establishment of SLE Mouse Model based on Balb/c Mice
    Tissue Sample Evaluation Index
    Urine Urine protein/
    Serum Anti-ds DNA antibody
    Blood biochemical index UREA
    CREA
    Pathological detection PAS staining
    H&E staining

    Content of Proteinuria in urine (A) and mouse Anti-dsDNA IgG in serum (B) were elevated after treatment with Pristane.

    Establishment of SLE Mouse Model based on B-hCD40 Mice

    Content of mouse Anti-dsDNA IgG in serum was decreased after treatment with anti-CD40 antibody in pristane-induced SLE B-hCD40 Mouse Model.