Microvascular Research Laboratory, Department of Orthopedic Surgery, Mayo Clinic, Rochester, Minnesota.
Department of Hand-, Plastic- and Reconstructive Surgery, Burn Center, BG Trauma Center Ludwigshafen, Germany.
Microsurgery. 2018 Feb;38(2):195-202. doi: 10.1002/micr.30255. Epub 2017 Nov 13.
Vascularized bone allotransplantation may provide new options for reconstruction of segmental defects if problems of long-term immune modulation can be solved. The current literature lacks an orthotopic large animal model, limited to bone and without the confounding effects of other tissue types, permitting a multifaceted evaluation before new methods are used clinically. The purpose of this study was to develop a large animal model for vascularized bone allotransplantation.
Eight porcine hind limbs were dissected. Length, diameter, and location of all hindlimb vessels were measured and a single nutrient vessel supplying the tibial diaphysis identified enabling its use as a vascularized bone allotransplant. Four Yucatan minipigs were divided into two pairs with a major swine leukocyte antigen mismatch. A 3.5 cm tibial segment including its nutrient pedicle was raised simultaneously from each pig and transplanted into the matched defect of the other animal. Microarterial anastomosis of the pedicle and 3-drug immunosuppression maintained VCA viability. Bone healing and limb function were followed for 16 weeks.
A consistent tibia diaphyseal nutrient artery arose from the caudal tibial artery to enter bone a mean 2.8 mm distal to the tibial tubercle with a pedicle length of 6.6 ± 3.3 mm and diameter of 1.6 ± 0.2 mm. Using this pedicle, we reconstructed a 3.5 cm tibial defect with a vascularized bone allotransplant in four animals. Immediate weightbearing as well as progressive bone healing was demonstrated.
We have developed a vascularized tibial bone allotranplantation large-animal model suitable for future bone-only allotranplantation research in mini-pigs.
如果能够解决长期免疫调节的问题,血管化骨同种异体移植可能为节段性缺损的重建提供新的选择。目前的文献缺乏一种原位大动物模型,仅限于骨骼,没有其他组织类型的混杂影响,在新方法用于临床之前,可以进行多方面的评估。本研究的目的是开发一种用于血管化骨同种异体移植的大动物模型。
解剖了 8 条猪后腿。测量了所有后肢血管的长度、直径和位置,并确定了一条单一的营养血管供应胫骨骨干,使其能够作为血管化骨同种异体移植。将 4 只尤卡坦微型猪分为两组,存在主要猪白细胞抗原不匹配。从每只猪同时抬起 3.5cm 的胫骨段及其营养蒂,并将其移植到另一只动物的匹配缺损处。蒂的微动吻合和 3 药物免疫抑制维持 VCA 活力。随访 16 周以观察骨愈合和肢体功能。
一条一致的胫骨骨干营养动脉从胫骨后动脉发出,进入骨骼的位置在胫骨结节下 2.8mm 处,蒂的长度为 6.6±3.3mm,直径为 1.6±0.2mm。使用这条蒂,我们在 4 只动物中重建了一个 3.5cm 的胫骨缺损和一个血管化骨同种异体移植。立即承重以及逐渐的骨愈合得到了证明。
我们已经开发出一种适合于未来在小型猪中进行单纯骨同种异体移植研究的血管化胫骨骨同种异体移植大动物模型。