Therapeutic Potential of a Senolytic Approach in a Murine Model of Chronic GVHD

Abstract

Graft-versus-host disease (GVHD) is a life-threatening systemic complication of allogeneic hematopoietic stem cell transplantation (HSCT) characterized by dysregulation of T and B cell activation and function, scleroderma-like features, and multi-organ pathology. The treatment of cGVHD is limited to the management of symptoms and long-term use of immunosuppressive therapy, which underscores the need for developing novel treatment approaches. Notably, there is a striking similarity between cytokines/chemokines responsible for multi-organ damage in cGVHD and pro-inflammatory factors, immune modulators, and growth factors secreted by senescent cells upon the acquisition of senescence-associated secretory phenotype (SASP). In this pilot study, we questioned the involvement of senescent cell-derived factors in the pathogenesis of cGVHD triggered upon allogeneic transplantation in an irradiated host. Using a murine model that recapitulates sclerodermatous cGVHD, we investigated the therapeutic efficacy of a senolytic combination of dasatinib and quercetin (DQ) administered after 10 days of allogeneic transplantation and given every 7 days for 35 days. Treatment with DQ resulted in a significant improvement in several physical and tissue-specific features, such as alopecia and earlobe thickness, associated with cGVHD pathogenesis in allograft recipients. DQ also mitigated cGVHD-associated changes in the peripheral T cell pool and serum levels of SASP-like cytokines, such as IL-4, IL-6 and IL-8Rα. Our results support the involvement of senescent cells in the pathogenesis of cGVHD and provide a rationale for the use of DQ, a clinically approved senolytic approach, as a potential therapeutic strategy.

The potential for senotherapy as a novel approach to extend life quality in veterinary medicine

“…Dasatinib Finally, dasatinib and quercetin have been investigated in several other unrelated disease processes in rodent models. In a murine model of sclerodermatous graft vs. host disease, the administration of a combination of dasatinib and quercetin led to a reduction in peripheral senescence-associated secretory phenotype (SASP) cytokines, specifically IL-4, IL-6, and IL-8Rα (106). In a mouse model of doxorubicin-induced ovarian injury, both dasatinib and quercetin and fisetin treatments reduced SC presence, however treatment was unable to restore normal ovarian function (107).…”