Harvard John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, Massachusetts 02138, USA.
Wyss Institute for Biologically Inspired Engineering, Cambridge, Massachusetts 02138, USA.
Biomater Sci. 2020 Jan 1;8(1):266-277. doi: 10.1039/c9bm01487j. Epub 2019 Nov 6.
Allotransplantation offers the potential to restore the anatomy and function of injured tissues and organs, but typically requires life-long, systemic administration of immunosuppressive drugs to prevent rejection, which can result in serious complications. Targeting the immunosuppressive drug to the graft favors local tissue concentration versus systemic drug exposure and end-organ toxicity. This could reduce the overall dose and dosing frequency of immunosuppressive drugs, and improve the safety and efficacy of treatment. Here, we developed dibenzocyclooctyne (DBCO)-modified prodrugs of the immunosuppressive drugs tacrolimus, rapamycin and mycophenolic acid, and demonstrated their targeted conjugation both in vitro and in vivo to azido-modified hydrogels via Click chemistry. Such azido-modified hydrogels placed in transplanted tissues enable sustained local release of drugs, and could be repeatedly refilled with systemically administered acid-labile prodrugs after drug exhaustion. Thus, clickable prodrugs with degradable linkers provide new possibilities for graft targeted immunosuppression in the context of allotransplantation.
同种异体移植有可能恢复受损组织和器官的解剖和功能,但通常需要终身、系统地使用免疫抑制药物来预防排斥反应,这可能会导致严重的并发症。将免疫抑制药物靶向移植物有利于局部组织浓度而不是全身药物暴露和终末器官毒性。这可以减少免疫抑制药物的总体剂量和给药频率,并提高治疗的安全性和疗效。在这里,我们开发了免疫抑制剂他克莫司、雷帕霉素和霉酚酸的二苯并环辛炔 (DBCO) 修饰前药,并通过点击化学证明了它们在体外和体内与叠氮修饰的水凝胶的靶向缀合。这种放置在移植组织中的叠氮修饰水凝胶能够持续释放药物,并在药物耗尽后,可以用系统给予的酸不稳定前药重复填充。因此,具有可降解连接物的可点击前药为同种异体移植背景下的移植物靶向免疫抑制提供了新的可能性。