Feng F Y, Ogden M A, Myckatyn T M, Grand A G, Jensen J N, Hunter D A, Mackinnon S E
Division of Plastic and Reconstructive Surgery, Washington University School of Medicine, St. Louis, Missouri, USA.
J Neurotrauma. 2001 Feb;18(2):217-29. doi: 10.1089/08977150150502631.
This study investigated the ability of the immunosuppressant FK506 to reverse nerve allograft rejection in progress. Eighty-four Buffalo rats received posterior tibial nerve grafts from either Lewis or Buffalo donor animals. Allografts were left untreated for either 7, 10, or 14 days before receiving daily subcutaneous FK506 injections (2 mg/kg). Time-matched control animals received either an isograft, an allograft with continuous FK506, or an allograft with no postoperative FK506 therapy. All animals underwent weekly evaluation of nerve function by walking track analysis. Experimental group animals were sacrificed either immediately prior to initiation of FK506 therapy (days 7, 10, or 14), after 2 weeks of immunosuppressive treatment, or 8 weeks postsurgery. Histomorphometric analysis, consisting of measurements of total number of nerve fibers, neural density, and percent of neural debris, demonstrated a statistically significant increase in regeneration in the isograft group relative to the untreated allograft group within 28 days of transplantation. Grafts harvested from animals receiving 2 weeks of FK506 after 7 or 10 days of rejection were histomorphometrically similar to time-matched isografts. By contrast, grafts from animals receiving 2 weeks of FK506 following 14 days without therapy resembled untreated allografts and demonstrated significant histomorphometric differences from isografts at the corresponding time point. Analysis of walking track data confirmed that relative to untreated allografts, functional recovery was hastened in animals receiving an isograft, or allograft treated with FK506. This study demonstrated that when started within 10 days of graft placement, FK506 could reverse nerve allograft rejection in rats evaluated following 2 weeks of treatment.
本研究调查了免疫抑制剂FK506逆转正在进行的神经同种异体移植排斥反应的能力。84只布法罗大鼠接受了来自Lewis或布法罗供体动物的胫后神经移植。同种异体移植在接受每日皮下注射FK506(2mg/kg)前,分别未治疗7天、10天或14天。时间匹配的对照动物接受同基因移植、持续使用FK506的同种异体移植或术后不进行FK506治疗的同种异体移植。所有动物每周通过行走轨迹分析对神经功能进行评估。实验组动物在开始FK506治疗前(第7天、10天或14天)、免疫抑制治疗2周后或术后8周处死。组织形态计量分析包括测量神经纤维总数、神经密度和神经碎片百分比,结果显示,移植后28天内,同基因移植组相对于未治疗的同种异体移植组,再生有统计学显著增加。在排斥反应7天或10天后接受2周FK506治疗的动物所取的移植物,在组织形态计量学上与时间匹配的同基因移植物相似。相比之下,在未经治疗14天后接受2周FK506治疗的动物所取的移植物类似于未治疗的同种异体移植物,并且在相应时间点与同基因移植物存在显著的组织形态计量学差异。行走轨迹数据分析证实,相对于未治疗的同种异体移植,接受同基因移植或用FK506治疗的同种异体移植的动物功能恢复加快。本研究表明,在移植后10天内开始使用时,FK506可逆转大鼠神经同种异体移植排斥反应,该反应在治疗2周后进行评估。