Department of Plastic and Reconstructive Surgery, University of Pittsburgh Medical Center, Pittsburgh, PA, USA.
Ann Surg. 2013 Feb;257(2):345-51. doi: 10.1097/SLA.0b013e31826d90bb.
To minimize maintenance immunosuppression in upper-extremity transplantation to favor the risk-benefit balance of this procedure.
Despite favorable outcomes, broad clinical application of reconstructive transplantation is limited by the risks and side effects of multidrug immunosuppression. We present our experience with upper-extremity transplantation under a novel, donor bone marrow (BM) cell-based treatment protocol ("Pittsburgh protocol").
Between March 2009 and September 2010, 5 patients received a bilateral hand (n = 2), a bilateral hand/forearm (n = 1), or a unilateral (n = 2) hand transplant. Patients were treated with alemtuzumab and methylprednisolone for induction, followed by tacrolimus monotherapy. On day 14, patients received an infusion of donor BM cells isolated from 9 vertebral bodies. Comprehensive follow-up included functional evaluation, imaging, and immunomonitoring.
All patients are maintained on tacrolimus monotherapy with trough levels ranging between 4 and 12 ng/mL. Skin rejections were infrequent and reversible. Patients demonstrated sustained improvements in motor function and sensory return correlating with time after transplantation and level of amputation. Side effects included transient increase in serum creatinine, hyperglycemia managed with oral hypoglycemics, minor wound infection, and hyperuricemia but no infections. Immunomonitoring revealed transient moderate levels of donor-specific antibodies, adequate immunocompetence, and no peripheral blood chimerism. Imaging demonstrated patent vessels with only mild luminal narrowing/occlusion in 1 case. Protocol skin biopsies showed absent or minimal perivascular cellular infiltrates.
Our data suggest that this BM cell-based treatment protocol is safe, is well tolerated, and allows upper-extremity transplantation using low-dose tacrolimus monotherapy.
最大限度地减少上肢移植的维持性免疫抑制,以利于该手术的风险效益平衡。
尽管上肢移植具有良好的结果,但由于多药物免疫抑制的风险和副作用,其广泛的临床应用受到限制。我们介绍了在一种新的供体骨髓(BM)细胞为基础的治疗方案(“匹兹堡方案”)下进行上肢移植的经验。
2009 年 3 月至 2010 年 9 月,5 例患者接受了双侧手(n = 2)、双侧手/前臂(n = 1)或单侧(n = 2)手移植。患者接受了阿仑单抗和甲基强的松龙诱导治疗,然后接受了他克莫司单药治疗。第 14 天,患者接受了来自 9 个椎体的供体 BM 细胞输注。综合随访包括功能评估、影像学和免疫监测。
所有患者均维持他克莫司单药治疗,谷浓度范围为 4 至 12ng/ml。皮肤排斥反应罕见且可逆转。患者的运动功能和感觉恢复持续改善,与移植后时间和截肢水平相关。副作用包括血清肌酐一过性升高、口服降糖药治疗的高血糖、轻微伤口感染和高尿酸血症,但无感染。免疫监测显示,短暂的中等水平的供体特异性抗体,足够的免疫能力,没有外周血嵌合体。影像学检查显示血管通畅,仅 1 例轻度管腔狭窄/闭塞。方案皮肤活检显示,无或极少的血管周围细胞浸润。
我们的数据表明,这种基于 BM 细胞的治疗方案是安全的,耐受性良好,并且可以使用低剂量他克莫司单药治疗上肢移植。