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骨髓嵌合诱导的耐受性可预防大鼠小肠移植慢性排斥模型中的移植血管硬化。

Tolerance induced by bone marrow chimerism prevents transplant vascular sclerosis in a rat model of small bowel transplant chronic rejection.

作者信息

Orloff S L, Yin Q, Corless C L, Orloff M S, Rabkin J M, Wagner C R

机构信息

Department of Surgery, Portland Veterans Affairs Medical Center, Oregon, USA.

出版信息

Transplantation. 2000 Apr 15;69(7):1295-303. doi: 10.1097/00007890-200004150-00015.

Abstract

BACKGROUND

The major impediment to success in solid organ transplantation is chronic rejection (CR). The characteristic lesion of CR is transplant vascular sclerosis (TVS). Although the mechanism of TVS is thought to have an immunologic basis, in humans immunosuppression does not prevent or reverse it. One possible therapy to prevent TVS is induction of donor-specific tolerance. Bone marrow chimerism has been successful in inducing tolerance in acute and chronic rejection heart and kidney transplant models. The highly immunogenic small bowel (SB) allograft provides a rigorous test of the efficacy of this tolerance regimen. We examined whether induction of tolerance by bone marrow chimerism could prevent TVS in a model of Fisher 344 (F344) to Lewis (LEW) rat SB transplantation.

METHODS

Bone marrow chimeras (BMC) were created by transplantation of T-cell-depleted F344 bone marrow into irradiated LEW rats. Chimerism was assessed by flow cytometric method. F344 SB, heterotopically transplanted into the chimeras, was clinically and histologically assessed for CR. F344 SB grafts, transplanted into cyclosporine-A-treated LEW recipients, served as control grafts for CR.

RESULTS

Cyclosporine-A-treated LEW rats chronically rejected F344 SB grafts. By contrast, the BMC group demonstrated tolerance and had long-term SB graft survival (>120 days) without TVS. The BMC demonstrated immunocompetence by prompt rejection of third party ACI (RT1av1) SB allografts.

CONCLUSIONS

Bone marrow chimerism prevents chronic graft failure secondary to TVS in a model of chronic SB rejection. TVS fails to develop when tolerance is established, suggesting that the mechanisms involved in TVS are, in part, immunologically mediated.

摘要

背景

实体器官移植成功的主要障碍是慢性排斥反应(CR)。CR的特征性病变是移植血管硬化(TVS)。尽管TVS的机制被认为有免疫基础,但在人类中免疫抑制并不能预防或逆转它。一种预防TVS的可能疗法是诱导供体特异性耐受。骨髓嵌合在急性和慢性排斥反应的心脏和肾脏移植模型中成功诱导了耐受。高免疫原性的小肠(SB)同种异体移植为这种耐受方案的疗效提供了严格的测试。我们研究了在Fisher 344(F344)到Lewis(LEW)大鼠SB移植模型中,通过骨髓嵌合诱导耐受是否能预防TVS。

方法

通过将去除T细胞的F344骨髓移植到经照射的LEW大鼠中创建骨髓嵌合体(BMC)。通过流式细胞术评估嵌合情况。将F344 SB异位移植到嵌合体中,对CR进行临床和组织学评估。将F344 SB移植物移植到用环孢素A治疗的LEW受体中,作为CR的对照移植物。

结果

用环孢素A治疗的LEW大鼠长期排斥F344 SB移植物。相比之下,BMC组表现出耐受,SB移植物长期存活(>120天)且无TVS。BMC通过迅速排斥第三方ACI(RT1av1)SB同种异体移植物表现出免疫活性。

结论

在慢性SB排斥模型中,骨髓嵌合可预防继发于TVS的慢性移植物衰竭。当建立耐受时,TVS不会发生,这表明参与TVS的机制部分是由免疫介导的。

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