Hisamatsu Chieko, Maeda Kosaku, Tanaka Hiroshi, Okita Yutaka
Department of Cardiovascular, Thoracic and Pediatric Surgery, Kobe University Graduate School of Medicine, 7-5-2, Kusunoki-cho, Chuo-ku, Kobe, 650-0017, Japan.
Pediatr Surg Int. 2006 Nov;22(11):881-5. doi: 10.1007/s00383-006-1757-x.
Transplantation of a cryopreserved tracheal allograft is considered to be a useful strategy in treating congenital tracheal stenosis. Recent reports of tracheal transplant experiments have shown that the antigenicity of the trachea is decreased by cryopreservation, making transplantation of the trachea possible. However, we reported that cryopreserved tracheal allografts exhibited favorable patency, but no significant growth in an animal model. In this study, we hypothesize that an immune reaction may play a role in the failure of an allograft's growth. Each allograft was harvested from 90- to 120-day-old Japanese rabbits, immersed in preservation solution, stored in a programmable freezer until it reached -80 C, and then kept for 1 month. Orthotopic tracheal transplantation of four tracheal rings in an end-to-end fashion was performed in age-matched young rabbits. Ten recipients were classified into three groups: a group provided with tacrolimus (FK-506) as an immunosuppressant (n = 6), a group receiving a graft irradiated before transplantation (n = 2), and a control group (n = 2). All grafts were evaluated 4-8 weeks after transplantation (tacrolimus group: 3-13 weeks). Body weight gain of the tacrolimus group was less than that of the other two groups. All grafts were well incorporated with the recipients macroscopically, but the grafts showed no growth in diameter. Microscopic examination showed inflammation in the tacrolimus and control groups temporarily. The irradiated allografts had marked fibrosis in the subepithelium. Although calcification of the tracheal cartilage was present in all transplanted allografts, the difference between groups was not significant. Patency of the cryopreserved tracheal allografts was favorable but no growth occurred even with an immunosuppressant. Further studies are required to address the growth of the tracheal allograft.
冷冻保存的气管同种异体移植被认为是治疗先天性气管狭窄的一种有效策略。最近关于气管移植实验的报道表明,气管的抗原性通过冷冻保存而降低,使得气管移植成为可能。然而,我们报道冷冻保存的气管同种异体移植在动物模型中表现出良好的通畅性,但没有显著生长。在本研究中,我们假设免疫反应可能在同种异体移植生长失败中起作用。每个同种异体移植取自90至120日龄的日本白兔,浸入保存液中,储存在程序降温冷冻器中直至达到-80℃,然后保存1个月。以端端方式将四个气管环原位气管移植到年龄匹配的幼兔中。10只受体被分为三组:一组给予他克莫司(FK-506)作为免疫抑制剂(n = 6),一组接受移植前照射的移植物(n = 2),以及一个对照组(n = 2)。所有移植物在移植后4至8周进行评估(他克莫司组:3至13周)。他克莫司组的体重增加低于其他两组。所有移植物在宏观上都与受体良好整合,但移植物直径没有生长。显微镜检查显示他克莫司组和对照组暂时有炎症。照射后的同种异体移植物在基底膜下有明显纤维化。虽然所有移植的同种异体移植物中气管软骨都有钙化,但组间差异不显著。冷冻保存的气管同种异体移植通畅性良好,但即使使用免疫抑制剂也没有生长。需要进一步研究来解决气管同种异体移植的生长问题