Nelson Marc, Fritz Michael, Dan Olivia, Worley Sarah, Strome Marshall
Department of Otolarynology and Communicative Disorders, The Cleveland Clinic Foundation, Ohio, 44195, USA.
Laryngoscope. 2003 Aug;113(8):1308-13. doi: 10.1097/00005537-200308000-00009.
OBJECTIVES/HYPOTHESIS: Tacrolimus is efficacious in several transplantation settings. Some studies have demonstrated improved results using combination therapy with mycophenolate mofetil. Our primary objective was to evaluate the efficacy and optimal dosing of tacrolimus in preventing rejection, using an established rat model of laryngeal transplantation. Further, the ability of mycophenolate to allow lower dosing of tacrolimus while achieving equivalent immunosuppression was investigated.
A dosage efficacy study with 10 experimental arms was conducted.
Dosage groups were 0.1, 0.2, 0.3, and 0.6 mg/kg tacrolimus alone and 0.1 mg/kg tacrolimus combined with 15 mg/kg mycophenolate mofetil, 0.1 mg/kg tacrolimus combined with 30 mg/kg mycophenolate mofetil, 0.1 mg/kg tacrolimus combined with 40 mg/kg mycophenolate mofetil, 0.2 mg/kg tacrolimus combined with 15 mg/kg mycophenolate mofetil, 0.2 mg/kg tacrolimus combined with 30 mg/kg mycophenolate mofetil (30 d only), and 0.2 mg/kg tacrolimus combined with 40 mg/kg mycophenolate mofetil. Each group contained 8 to 10 rats. Grafts were harvested for histopathological analysis on day 15 or 30 after transplantation. Histopathological appearance of the graft was blindly graded according to an established scale. Dosage groups were compared on rejection score using Wilcoxon's rank sum test and the Jonckheere-Terpstra test for trend.
There was a significant association between increasing dose of tacrolimus and decreasing rejection score at both 15 and 30 days (P <.001). In the groups treated with 0.1 mg/kg T, an increasing dose of mycophenolate was associated with lower rejection scores at both 15 and 30 days (P =.001). In the group treated with 0.2 mg/kg T, there was no evidence that the addition of mycophenolate resulted in lower rejection at 15 days. However, at 30 days, combination therapy with increasing doses of mycophenolate was associated with decreasing rejection score (P =.002).
Tacrolimus is an effective immunosuppressive agent for laryngeal transplantation. Mycophenolate mofetil allows lower doses of tacrolimus to be used while preserving graft viability in the early post-transplantation period.
目的/假设:他克莫司在多种移植环境中均有效。一些研究表明,联合霉酚酸酯进行治疗可取得更好的效果。我们的主要目的是使用已建立的大鼠喉移植模型,评估他克莫司在预防排斥反应方面的疗效和最佳剂量。此外,还研究了霉酚酸在实现等效免疫抑制的同时允许降低他克莫司剂量的能力。
进行了一项包含10个实验组的剂量疗效研究。
剂量组分别为单独使用0.1、0.2、0.3和0.6mg/kg他克莫司,以及0.1mg/kg他克莫司与15mg/kg霉酚酸酯联合使用、0.1mg/kg他克莫司与30mg/kg霉酚酸酯联合使用、0.1mg/kg他克莫司与40mg/kg霉酚酸酯联合使用、0.2mg/kg他克莫司与15mg/kg霉酚酸酯联合使用、0.2mg/kg他克莫司与30mg/kg霉酚酸酯联合使用(仅30天),以及0.2mg/kg他克莫司与40mg/kg霉酚酸酯联合使用。每组包含8至10只大鼠。在移植后第15天或30天采集移植物进行组织病理学分析。根据既定标准对移植物的组织病理学外观进行盲法评分。使用Wilcoxon秩和检验和Jonckheere-Terpstra趋势检验对剂量组的排斥评分进行比较。
在第15天和第30天,他克莫司剂量增加与排斥评分降低之间均存在显著相关性(P<.001)。在使用0.1mg/kg他克莫司治疗的组中,霉酚酸剂量增加与第15天和第30天的排斥评分降低相关(P=.001)。在使用0.2mg/kg他克莫司治疗的组中,没有证据表明添加霉酚酸在第15天会导致排斥反应降低。然而,在第30天,霉酚酸剂量增加的联合治疗与排斥评分降低相关(P=.002)。
他克莫司是一种有效的喉移植免疫抑制剂。霉酚酸酯可在移植后早期降低他克莫司的使用剂量,同时保持移植物的存活能力。