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Updated: May 11, 2026

The bm12 Inducible Model of Systemic Lupus Erythematosus (SLE) in C57BL/6 Mice
Published on: November 1, 2015
Targeting the complement system in systemic lupus erythematosus and other diseases
Maria-Louise Barilla-Labarca1, Kiley Toder, Richard Furie
1Division of Rheumatology and Allergy-Immunology, North Shore-Long Island Jewish Health System, Hofstra North Shore-LIJ School of Medicine, 865 Northern Boulevard Suite 302, Great Neck, NY 11021, USA.
Complement inhibitors are overlooked in systemic lupus erythematosus (SLE) treatments despite evidence from mouse models and limited human studies. Further research into complement inhibition for SLE is warranted, drawing parallels from other inflammatory diseases.
Area of Science:
- Immunology
- Rheumatology
- Pathogenesis of Autoimmune Diseases
Background:
- The complement system plays a crucial role in the pathogenesis of systemic lupus erythematosus (SLE).
- Despite extensive clinical trials for SLE, complement inhibitors have not been a focus of therapeutic strategies.
- Existing research in murine lupus models suggests potential benefits of complement inhibition.
Purpose of the Study:
- To review scientific data from murine lupus models supporting the investigation of complement inhibitors in human SLE.
- To analyze the existing study of eculizumab, a complement inhibitor, in SLE patients.
- To explore how complement inhibitor development in other inflammatory diseases could inform SLE treatment strategies.
Main Methods:
- Review of scientific literature on murine lupus models.
- Analysis of the single published study involving eculizumab in SLE patients.
- Examination of ongoing complement inhibitor programs in other inflammatory conditions.
Main Results:
- Murine lupus data provide a scientific rationale for exploring complement inhibition in human SLE.
- The sole study of eculizumab in SLE patients offers preliminary insights.
- Other inflammatory diseases show promise for complement inhibitor development.
Conclusions:
- Complement inhibition represents a potential therapeutic avenue for systemic lupus erythematosus (SLE).
- Further clinical investigation of complement inhibitors in SLE is justified, informed by preclinical data and experiences in other diseases.
- The development of complement inhibitors for SLE could be accelerated by leveraging knowledge from related inflammatory conditions.
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