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The bm12 Inducible Model of Systemic Lupus Erythematosus (SLE) in C57BL/6 Mice
Published on: November 1, 2015
Gallium nitrate suppresses lupus in MRL/lpr mice
G Apseloff1, K V Hackshaw, C Whitacre
1Department of Pharmacology, College of Medicine, The Ohio State University, Columbus 43210-1239, USA.
Naunyn-Schmiedeberg'S Archives of Pharmacology
|January 24, 1998
Summary
Gallium nitrate (Ga) treatment reduced disease severity in a murine model of systemic lupus erythematosus (SLE). Ga administration decreased lymph node size and lymphoid infiltrate, showing potential for SLE therapy.
Area of Science:
- Immunology
- Pharmacology
- Rheumatology
Background:
- Systemic lupus erythematosus (SLE) is a chronic autoimmune disease.
- Experimental autoimmune diseases are prevented by Gallium (Ga) nitrate.
- Murine models are crucial for studying SLE pathogenesis and potential treatments.
Purpose of the Study:
- To investigate the efficacy of Gallium (Ga) nitrate in a murine model of systemic lupus erythematosus (SLE).
- To evaluate the impact of Ga on disease indicators such as lymph node size, lymphoid infiltrate, and organ pathology.
- To assess the immunological effects of Ga, including lymphocyte populations and responses.
Main Methods:
- MRL/Mp lpr/lpr (MRL/lpr) mice were treated with Gallium (Ga) nitrate or vehicle control.
- Subcutaneous injections of Ga were administered weekly, with varying doses and durations.
- Disease progression was assessed by measuring lymph node and spleen weights, lymphoid infiltration, and histological examination of organs.
Main Results:
- Ga-treated mice exhibited significantly smaller lymph nodes and reduced lymphoid infiltrate compared to controls.
- Ga administration mitigated glomerulitis and renal vasculitis, observed in control mice.
- Ga treatment led to increased CD4+ and CD8+ lymphocytes and enhanced lymph node proliferative responses in vitro.
Conclusions:
- Gallium (Ga) nitrate demonstrates therapeutic potential in a murine model of SLE.
- Ga treatment reduced key pathological features of SLE, including organ inflammation and lymphoid abnormalities.
- Further clinical trials with Ga for SLE are warranted based on these preliminary findings.

