| Literature DB >> 34373602 |
Erika M J Siren1,2, Haiming D Luo1,2, Franklin Tam3, Ashani Montgomery3, Winnie Enns3, Haisle Moon1,4, Lyann Sim2, Kevin Rey3, Qiunong Guan5, Jiao-Jing Wang6, Christine M Wardell7,8, Mahdis Monajemi7,8, Majid Mojibian7,8, Megan K Levings7,8,9, Zheng J Zhang6, Caigan Du5, Stephen G Withers2, Jonathan C Choy10, Jayachandran N Kizhakkedathu11,12,13,14.
Abstract
Systemic immunosuppression for the mitigation of immune rejection after organ transplantation causes adverse side effects and constrains the long-term benefits of the transplanted graft. Here we show that protecting the endothelial glycocalyx in vascular allografts via the enzymatic ligation of immunosuppressive glycopolymers under cold-storage conditions attenuates the acute and chronic rejection of the grafts after transplantation in the absence of systemic immunosuppression. In syngeneic and allogeneic mice that received kidney transplants, the steric and immunosuppressive properties of the ligated polymers largely protected the transplanted grafts from ischaemic reperfusion injury, and from immune-cell adhesion and thereby immunocytotoxicity. Polymer-mediated shielding of the endothelial glycocalyx following organ procurement should be compatible with clinical procedures for transplant preservation and perfusion, and may reduce the damage and rejection of transplanted organs after surgery.Entities:
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Year: 2021 PMID: 34373602 DOI: 10.1038/s41551-021-00777-y
Source DB: PubMed Journal: Nat Biomed Eng ISSN: 2157-846X Impact factor: 25.671