RESUMEN
The chronic rejection responses and side effects of the systematic administration of immunosuppressants are the main obstacles to heart allograft and patient survival. The development of xenotransplantation also urgently requires more efficient immune regulation strategies. Herein, it is demonstrated that lymph-node (LN)-targeted drug delivery can realize LN-specific immunomodulation with attenuated immune suppression on distant peripheral immune organs to effectively prolong long-term survival after heart transplantation in a chronic murine heart transplantation model. A chemokine C-C motif ligand 21 (CCL21) specific aptamer for LN targeting is decorated onto the surface of the hybrid nanoparticular delivery vector mainly composed of CaCO3 /CaP/heparin. The targeting delivery system can dramatically enhance accumulation of the loaded immunosuppressant, fingolimod hydrochloride (FTY720), in draining lymph nodes (dLNs) for inducing powerful immune suppression. By promoting the generation of endogenous regulatory T cells (Tregs ) and decreasing the proportion of effector T cells (Teffs ) in dLNs after heart transplantation, the LN-targeting strategy can effectively regulate local immune responses instead of systemic immunity, which reduces the incidence of long-term complications. This study provides an efficient strategy to improve the survival rate after organ transplantation by precise and localized immunoregulation with minimized side effects of immunosuppression.
Asunto(s)
Trasplante de Corazón , Ganglios Linfáticos , Ratones , Humanos , Animales , Sistemas de Liberación de Medicamentos , Inmunosupresores/farmacología , Clorhidrato de Fingolimod/farmacología , Tolerancia Inmunológica , Inmunidad , InmunomodulaciónRESUMEN
OBJECTIVE: To study the chemical constituents from Lithocarpus polystachyus. METHODS: Compounds were isolated and purified with silica gel, and there structures were identified by chemical property and spectral data. RESULTS: Nine compounds were isolated as phloridzin (I), phloretin (II), dihydrochalcone-2'-beta-D-glucopyranoside (III), daucossterol (IV), beta-sitosterol (V), quercetin (VI), luteolin (VII), quercitrin (VI), oleanolic acid (IX). CONCLUSION: Compounds II, IV - IX are isolated from this plant for the first time.