Hale D A, Waldorf K A, Kleinschmidt J, Pearl R H, Seyfer A E
General and Plastic Surgery Services, Walter Reed Army Medical Center, Washington, DC.
J Pediatr Surg. 1991 Aug;26(8):914-20. doi: 10.1016/0022-3468(91)90836-i.
Small intestinal transplantation represents a potentially therapeutic procedure for individuals with short gut syndrome. The purpose of this study was to develop a model for small intestinal transplantation in primates that is: technically feasible without microsurgery; consistent in the prevention of allograft rejection; functional in terms of nutrient absorption; and compatible with harvest for multiple organ procurement. First, autotransplantations on four rhesus monkeys were performed in order to study a variety of harvesting techniques and vascular anastomoses. Then, a study was performed with 14 heterotopic allotransplants in 4 baboons and 10 rhesus primates. The successful donor model consisted of division of the pancreas, harvesting the small bowel with a superior mesenteric artery and portal vein pedicle. The allograft vascular pedicle was anastomosed to the recipient's common iliac vessels in end-to-side fashion. The graft was transplanted as an out-of-continuity loop, both ends being exteriorized as stomas providing access for absorption studies and biopsy. Three immunosuppressive regimens were tested: (1) cyclosporine A (CyA) 20 mg/kg/d, solumedrol (SML) 2 mg/kg/d, and graft irradiation (150 rad) (n = 4); (2) CyA 20 mg/kg/d and SML 2 mg/kg/d (n = 3); and (3) CyA 40 mg/kg/d, SML 2 mg/kg/d, and azathioprine 5 mg/kg/d (n = 3). There were 4 deaths due to technical error in the first 24 hours. Weekly graft biopsy, serum CyA levels, complete blood count, and automated 24-channel serum analysis were performed. Grafts surviving greater than 14 days underwent absorption study via luminal perfusion with sucrose, maltose, dextrose, Pregestimil, xylose, and cyclosporine.(ABSTRACT TRUNCATED AT 250 WORDS)
小肠移植对于短肠综合征患者而言是一种具有潜在治疗作用的手术。本研究的目的是建立一种灵长类动物小肠移植模型,该模型应具备以下特点:无需显微外科技术即可在技术上可行;在预防同种异体移植排斥方面具有一致性;在营养吸收方面具有功能性;并且与多器官获取时的小肠采集相兼容。首先,对四只恒河猴进行自体移植,以研究多种采集技术和血管吻合方法。然后,在4只狒狒和10只恒河猴中进行了14次异位同种异体移植研究。成功的供体模型包括将胰腺分离,以肠系膜上动脉和门静脉蒂采集小肠。将同种异体移植血管蒂以端侧方式吻合到受体的髂总血管。移植物作为不连续的肠袢进行移植,两端作为造口引出,以便进行吸收研究和活检。测试了三种免疫抑制方案:(1)环孢素A(CyA)20mg/kg/d、甲泼尼龙(SML)2mg/kg/d和移植物照射(150rad)(n = 4);(2)CyA 20mg/kg/d和SML 2mg/kg/d(n = 3);(3)CyA 40mg/kg/d、SML 2mg/kg/d和硫唑嘌呤5mg/kg/d(n = 3)。在前24小时内有4只动物因技术失误死亡。每周进行移植物活检、血清CyA水平检测、全血细胞计数和自动24通道血清分析。存活超过14天的移植物通过向肠腔灌注蔗糖、麦芽糖、葡萄糖、纽迪希亚、木糖和环孢素进行吸收研究。(摘要截短于250字)