Tojo T, Kitamura S, Gojo S, Kushibe K, Nezu K, Taniguchi S
Department of Surgery, Nara Medical University, Kashihara, Japan.
J Thorac Cardiovasc Surg. 1998 Oct;116(4):624-7. doi: 10.1016/S0022-5223(98)70169-2.
We investigated the origin of the epithelium in transplanted cryopreserved tracheal allografts in rats and tried to clarify the mechanism by which immunogenicity is reduced in this procedure.
Tracheal transplantation was performed with PVG rats (allele at the RT1 locus: c) used as donors and ACI rats (allele at the RT1 locus: a) as recipients. After resection of a 5-ring segment of the cervical trachea of an ACI rat, the trachea was reconstructed with the cryopreserved tracheal segment of a PVG rat (n = 6). No immunosuppressive agents or steroids were given. Histologic changes were determined and immunohistochemical staining was performed to investigate major histocompatibility complex class I antigens of the transplanted tracheal segment.
Two months after tracheal transplantation, 6 surviving ACI rats were killed. Histologically, the epithelium and tracheal cartilage of the transplanted cryopreserved segment displayed normal structure. Immunohistochemical staining showed that the major histocompatibility complex class I antigen of the ACI rat was expressed in the epithelium of the transplanted segment and that the class I antigen of the PVG rat was expressed in the cartilage of the transplanted segment.
After transplantation of the cryopreserved trachea, the epithelium of the transplanted cryopreserved segment originated from the recipient epithelium whereas the cartilage retained the structure of the donor trachea. We hypothesize that transplantation of a cryopreserved trachea leads to the growth of the recipient's epithelium over the donor trachea, thereby reducing the antigenicity of the transplant.
我们研究了大鼠同种异体冷冻保存气管移植上皮的来源,并试图阐明该过程中免疫原性降低的机制。
以PVG大鼠(RT1位点等位基因:c)作为供体,ACI大鼠(RT1位点等位基因:a)作为受体进行气管移植。切除ACI大鼠颈段气管的5环节段后,用PVG大鼠的冷冻保存气管节段重建气管(n = 6)。未给予免疫抑制剂或类固醇。确定组织学变化,并进行免疫组织化学染色以研究移植气管节段的主要组织相容性复合体I类抗原。
气管移植两个月后,处死6只存活的ACI大鼠。组织学上,移植的冷冻保存节段的上皮和气管软骨结构正常。免疫组织化学染色显示,ACI大鼠的主要组织相容性复合体I类抗原在移植节段的上皮中表达,而PVG大鼠的I类抗原在移植节段的软骨中表达。
冷冻保存气管移植后,移植的冷冻保存节段的上皮起源于受体上皮,而软骨保留了供体气管的结构。我们推测,冷冻保存气管的移植导致受体上皮在供体气管上生长,从而降低了移植的抗原性。