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 addition, we have generated over 900 human target KI mice covering SLE-related targets for testing various drugs.

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  • Systemic Lupus Erythematosus (SLE) Mouse Model
  • Pristane-Induced Systemic Lupus Erythematosus (SLE) Mouse Model
  • Balb/c mice
  • B-hCD40 mice
  • Spontaneous Systemic Lupus Erythematosus (SLE) Mouse Model
  • MRL/lpr mice
  • Our Services for Nephropathy Model

Related Resources

    Systemic Lupus Erythematosus (SLE) Mouse Model
    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 pristane develop an ascitic fluid enriched with monoclonal antibodies, local chronic inflammation (lipogranulomas), and a rheumatoid-like erosive arthritis. These clinical manifestations resemble SLE.
    Biocytogen offers pristane-induced SLE mouse models and MRL/lpr spontaneous SLE mouse models for pharmacological and efficacy evaluation of SLE therapeutics. Additionally, we have generated over 900 human target KI mouse models covering SLE-related targets to support the testing of a wide range of drug candidates.
    Pristane-Induced Systemic Lupus Erythematosus (SLE) Mouse Model
    Establishment of Pristane-Induced SLE Mouse Model in 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
    Establishment of pristane-induced SLE mouse model in Balb/c mice. Content of proteinuria in urine (A) and mouse anti-dsDNA IgG in serum (B) were elevated after treatment with pristane.
    Establishment of Pristane-Induced SLE Mouse Model in CD40 Humanized Mice (B-hCD40 Mice)
    Establishment of Pristane-Induced SLE Mouse Model in 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.