Abstract
BXSB mice, a murine model of systemic lupus erythematosus (SLE), were treated with two different doses of fludarabine for a four-week period and examined two weeks after the final dose. Control mice were treated with saline or cyclophosphamide. Mice treated with fludarabine had a significant reduction in renal pathology compared to control mice. Fludarabine-treated mice also had an almost 10-fold increase in percentile of CD8+CD25+ T cells in the spleen and a smaller but significant increase in CD4+CD25+ cells. Mice treated with cyclophosphamide had a greater leucopenia compared to the other groups and a significant reduction in percentile of B220+ cells in peripheral blood and spleen. Serum autoantibody levels to dsDNA did not differ significantly among the groups, but were higher in 4/10 mice treated with fludarabine. Although few trials of fludarabine for human SLE have been conducted, additional studies may be warranted.
| Original language | English |
|---|---|
| Pages (from-to) | 912-916 |
| Number of pages | 5 |
| Journal | Lupus |
| Volume | 13 |
| Issue number | 12 |
| DOIs | |
| State | Published - 2004 |
Keywords
- Cyclophosphamide
- Fludarabine
- Lupus
- Mouse
- Nephritis