Centre for Blood Research, Life Sciences Institute, The University of British Columbia, Vancouver, British Columbia, Canada.
Department of Chemistry, The University of British Columbia, Vancouver, British Columbia, Canada.
Nat Biomed Eng. 2021 Oct;5(10):1202-1216. doi: 10.1038/s41551-021-00777-y. Epub 2021 Aug 9.
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.
器官移植后,为减轻免疫排斥而进行的全身性免疫抑制会产生不良反应,并限制移植移植物的长期获益。在这里,我们表明,在冷储存条件下通过酶促连接免疫抑制糖聚物来保护血管同种异体移植物中的内皮糖萼,可以在不进行全身性免疫抑制的情况下减轻移植物移植后的急性和慢性排斥反应。在接受肾移植的同基因和同种异体小鼠中,连接聚合物的空间和免疫抑制特性在很大程度上保护了移植移植物免受缺血再灌注损伤以及免疫细胞黏附,从而避免免疫细胞毒性。器官获取后通过聚合物对内皮糖萼进行的屏蔽作用应该与移植保存和灌注的临床程序兼容,并且可能会降低手术后移植器官的损伤和排斥反应。