Tung Thomas H, Doolabh Vaishali B, Mackinnon Susan B, Mohanakumar T, Hicks Marshall E
Division of Plastic and Reconstructive Surgery, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
J Reconstr Microsurg. 2006 Aug;22(6):443-9. doi: 10.1055/s-2006-947699.
In this study, the authors evaluated whether the pretransplant portal venous administration of UV-B irradiated donor alloantigen would induce tolerance to long peripheral nerve allografts in a swine model. They completed nerve allograft transplantation between four swine of separate lineages. Regeneration across the nerve allografts was followed for 10 months postoperatively. Sequential IN VITRO assays demonstrated the successful and prolonged suppression of the recipient immune response to donor antigen following antigen inoculation. Histomorphometric analysis demonstrated successful regeneration across the long nerve allografts in the pretreated recipients, but not across allografts in unimmunosuppressed recipients. A single pretransplant antigen delivery protocol has the potential to replace chronic medicinal immunosuppressant therapy and its associated morbidities. Furthermore, tolerance to long nerve allografts has immediate applicability to clinical requirements for bridging multiple, complex, long nerve gaps.
在本研究中,作者评估了移植前经门静脉给予紫外线B照射的供体同种异体抗原是否会在猪模型中诱导对长外周神经同种异体移植的耐受性。他们在四个不同谱系的猪之间完成了神经同种异体移植。术后对神经同种异体移植的再生情况进行了10个月的跟踪。连续的体外试验表明,抗原接种后受体对供体抗原的免疫反应得到了成功且持久的抑制。组织形态计量学分析表明,预处理受体的长神经同种异体移植实现了成功再生,但未免疫抑制受体的同种异体移植未实现成功再生。单一的移植前抗原递送方案有可能取代慢性药物免疫抑制治疗及其相关并发症。此外,对长神经同种异体移植的耐受性可直接应用于弥合多个复杂长神经间隙的临床需求。