Yuan-Xin L, Ning L, You-Sheng L, Xiao-Dong N, Ming L, Jian W, Jie-Shou L
Research Institute of General Surgery, Jinling Hospital, Medical School of Nanjing University, Nanjing, China.
Transplant Proc. 2010 Jan-Feb;42(1):29-34. doi: 10.1016/j.transproceed.2009.12.028.
The goal of combining alemtuzumab induction therapy with low-dose tacrolimus monotherapy in small-bowel transplantation (SBTx) is to enable improved graft acceptance without immunologic unresponsiveness caused by stronger immunosuppression regimens. Herein, we report preliminary experience using this protocol in 5 patients who underwent SBTx in China.
Patients received methylprednisolone sodium succinate (Solu-Medrol), 1 g, followed by alemtuzumab infusion, 30 mg, during SBTx and another gram of prednisolone before reperfusion. Tacrolimus monotherapy without steroid was used for maintenance immunosuppression. Tacrolimus trough levels were 10 to 15 ng/dL during the first 3 months, and weaned to 5 to 10 ng/mL after 3 months.
Three recipients have survived for longer than 1 year; 1 patient is currently alive at 9 months, and another at 5 months post-SBTx. Grafts in these 5 recipients achieved excellent function, and in all patients, total parenteral nutrition was discontinued at 2 to 3 weeks postoperatively and normal oral intake was resumed. One recipient died at 13 months post-SBTx of severe rejection; the condition of the other 4 recipients who were still alive was good. Pathologic analysis of ileoscopic biopsy specimens revealed 4 episodes of indeterminate to mild acute cellular rejection (ACR) at 1 to 3 months, 3 episodes of indeterminate to mild ACR at 4 to 6 months, 3 episodes of moderate ACR at 7 to 12 months, and 1 episode of severe ACR at 13 months. All episodes of indeterminate to moderate ACR were totally resolved; only treatment of severe ACR failed. One patient experienced an episode of invasive fungal infection and another episode of cytomegaloviral infection, with total recovery after treatment.
Our preliminary experience in these 5 cases showed that the protocol combining alemtuzumab induction therapy with low-dose tacrolimus monotherapy without maintenance steroid therapy past-SBTx can effectively control rejection with excellent graft function. Nevertheless, close surveillance of ACR should be still performed after 6 months.
在小肠移植(SBTx)中,将阿仑单抗诱导治疗与低剂量他克莫司单一疗法相结合的目标是在不出现因更强免疫抑制方案导致的免疫无反应性的情况下,提高移植物的接受率。在此,我们报告在中国对5例接受SBTx的患者使用该方案的初步经验。
患者在SBTx期间接受1 g琥珀酸甲泼尼龙(甲强龙),随后输注30 mg阿仑单抗,并在再灌注前再给予1 g泼尼松龙。维持免疫抑制采用无类固醇的他克莫司单一疗法。最初3个月他克莫司谷浓度为10至15 ng/dL,3个月后减至5至10 ng/mL。
3例受者存活超过1年;1例患者在SBTx后9个月时仍存活,另1例在5个月时仍存活。这5例受者的移植物功能良好,所有患者在术后2至3周停止全胃肠外营养并恢复正常经口摄入。1例受者在SBTx后13个月死于严重排斥反应;其他4例仍存活的受者情况良好。回肠镜活检标本的病理分析显示,在1至3个月时有4次不确定至轻度急性细胞排斥反应(ACR),4至6个月时有3次不确定至轻度ACR,7至12个月时有3次中度ACR,13个月时有1次严重ACR。所有不确定至中度ACR发作均完全缓解;仅严重ACR的治疗失败。1例患者发生1次侵袭性真菌感染和1次巨细胞病毒感染,治疗后完全康复。
我们在这5例患者中的初步经验表明,SBTx后将阿仑单抗诱导治疗与低剂量他克莫司单一疗法相结合且不进行维持类固醇治疗的方案可有效控制排斥反应,移植物功能良好。然而,6个月后仍应密切监测ACR。