Li Yuan-Xin, Li Ning, Ni Xiao-Dong, Li You-Sheng, Li Min, Shen Jing, Li Jie-Shou
Research Institute of General Surgery, Nanjing General Hospital of Nanjing Military Command, Nanjing 210002, China.
Zhonghua Wai Ke Za Zhi. 2009 Jun 1;47(11):810-3.
To report preliminary experience of the protocol of combining Campath 1H induction with low-dose monotherapy of tacrolimus and no steroid in two cases of small bowel transplantation.
Campath 1H 30 mg was infused during the small bowel transplantation, and the patients were given 1 gram of methylprednisolone followed by the Campath 1H and another gram of methylprednisolone before reperfusion. Tacrolimus was infused just after the reperfusion. The tacrolimus was administered from vein first and then from gut tract, the blood tacrolimus level was controlled at 10 to 15 microg/L within the first 3 months after the operation, and reduced to 5 microg/L thereafter.
The two recipients have survived more than 1 year, one received surgical closure of intestinal graft terminal stoma 13 months after the transplantation. One episode of indeterminate to mild acute rejection was verified by pathology through routine ileoscopical biopsy in each cases, and one episode of mild to moderate acute rejection occurred 8 months after the transplantation, and the patients recovered after low dose or bolus steroid therapy. The peripheral lymphocyte counts and monocyte counts decreased greatly after Campath 1H was given, and recovered very slowly thereafter. No sign of infection and graft versus host disease (GVHD) was found, and the grafted intestine achieved excellent function. The total parenteral nutrition was ceased on the day 21 and 14 after the operation, respectively, and the patients lived on oral intake to maintain nutrition status.
It's showed that the protocol combining Campath 1H induction with low-dose monotherapy of tacrolimus without steroid in small bowel transplantation can control graft rejection effectively without increasing the opportunity of infection, no sign of GVHD is found, and the grafted intestine could achieve excellent function.
报告两例小肠移植中使用Campath 1H诱导联合低剂量他克莫司单药及无类固醇治疗方案的初步经验。
在小肠移植期间输注30mg Campath 1H,患者在Campath 1H输注前给予1克甲泼尼龙,再灌注前给予另一克甲泼尼龙。再灌注后立即输注他克莫司。他克莫司先经静脉给药,然后经肠道给药,术后前3个月将血他克莫司水平控制在10至15μg/L,此后降至5μg/L。
两名受者均存活超过1年,其中一名在移植后13个月接受了肠移植末端造口的手术闭合。通过常规回肠镜活检病理证实,每例均有一次不确定至轻度急性排斥反应,移植后8个月发生一次轻度至中度急性排斥反应,经低剂量或大剂量类固醇治疗后患者康复。给予Campath 1H后外周淋巴细胞计数和单核细胞计数大幅下降,此后恢复缓慢。未发现感染和移植物抗宿主病(GVHD)迹象,移植肠功能良好。术后第21天和第14天分别停止全胃肠外营养,患者通过口服维持营养状态。
结果显示,小肠移植中Campath 诱导联合低剂量他克莫司单药及无类固醇治疗方案可有效控制移植物排斥反应,且不增加感染机会,未发现GVHD迹象,移植肠功能良好。 1H