1201 SGLT2 inhibitors modulate inflammation and germinal centers in lupus

Background/Purpose Nephritis is one of the most severe manifestations in lupus, affecting 40–70% of patients. Though immune targeted therapies have improved, a significant number of patients experience renal damage and even progression to end stage renal disease (ESRD). Recently, sodium and glucose cotransporter 2 inhibitors (SGLT2i) have proven efficacious in preventing adverse renal outcomes in patients with a variety of chronic diseases. The mechanisms of protection by SGLT2i include their capacity to modulate hypoxia and fibrosis. Other literature supports a role for local hypoxia in the lupus nephritis (LN) kidney in driving pathogenic immune cell function, including in CD8 T cells. Here, we hypothesized that by alleviating hypoxia, SGLT2i will modulate local inflammation and fibrosis in lupus nephritis. Methods 10 weeks old MRL/lpr female mice were daily treated with dapagliflozin at 10 mg/kg or vehicle by gavage for 11 weeks. Sera was collected to measure autoantibodies and creatinine by ELISA. Immune cells and SGLT2 expression were quantitated in the spleen, renal lymph nodes (RLNs) and kidneys by flow cytometry and immunofluorescence. Inflammation, fibrosis, and infiltration by CD8 T cells or regulatory T cells were assessed in kidneys of MRL/lpr mice at baseline and 8 weeks after starting SGLT2i therapy. Results Consistent with a slow induction of SGLT2i therapeutic effect in humans and despite the efficient targeting of SGLT2 in MRL/lpr mice, proteinuria was not affected after 11 weeks of daily SGLT2i administration. Unexpectedly SGLT2i therapy had a remarkable impact on the formation of germinal centers (GCs) and the production of autoreactive plasma cells in the spleen. In line with the induction of regulatory T cells by SGLT2i in diabetic kidney disease, T follicular helper cells with a regulatory phenotype significantly increased in the GCs. In addition, skin and lymph node inflammation were attenuated by SGLT2i. However, inflammatory cell infiltration in the kidney was not affected by SGLT2i (figure 1). Conclusions Despite modest effects on kidney inflammation, SGLT2i surprisingly modulated splenic autoreactive GCs via significant accumulation of T follicular regulatory T cells, impairing the production of autoreactive plasma cells. One of the potential explanations for the modest kidney effects is the rapid disease progression in MRL/lpr mice and the slow therapeutic induction with SGLT2i. Thus, future studies are planned in NZB/NZW mice treated for longer periods of time and with combination immune suppressive therapy. Supported by a Lupus Mechanisms and Targets Award from the Lupus Research Alliance