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重建移植后多次急性排斥反应后的复合组织血管病和变性。

Composite tissue vasculopathy and degeneration following multiple episodes of acute rejection in reconstructive transplantation.

机构信息

Division of Plastic Surgery, University of Pittsburgh Medical Center, Pittsburgh, PA, USA.

出版信息

Am J Transplant. 2010 Feb;10(2):251-61. doi: 10.1111/j.1600-6143.2009.02941.x. Epub 2009 Dec 23.

DOI:10.1111/j.1600-6143.2009.02941.x
PMID:20041866
Abstract

Transplant vasculopathy has not been systematically investigated in composite tissue allotransplantation (CTA). The impact of multiple acute rejections (ARs) on long-term graft outcomes in reconstructive transplantation remains unknown. This study in a rat hind-limb allotransplantation model systematically analyzes vasculopathy and tissue-specific pathological changes secondary to multiple AR episodes. LEW rats were transplanted with BN rat hind limbs and treated as follows: Group 1 (Iso): isografts. Group 2 (CsA): Cyclosporine (CsA) qd; Group 3 (mult AR): CsA and dexamethasone only when AR was observed. No AR was observed in Groups 1 and 2. Multiple AR were observed in Group 3, and each episode was completely reversed (clinically) with pulsed CsA + dexamethasone treatment. Group 3 animals demonstrated significant vascular lesions along with skin and muscle atrophy, upregulation of profibrotic gene expression and fibrosis when compared to Groups 1 and 2. In addition, allograft bone was sclerotic, weak and prone to malunion and nonunion. Interestingly, vasculopathy was a late finding, whereas muscle atrophy with macrophage infiltration was seen early, after only a few AR episodes. Taken together, multiple AR episodes lead to vasculopathy and tissue-specific pathology in CTA. This is the first evidence of 'composite tissue vasculopathy and degeneration (CTVD)' in CTA.

摘要

移植血管病在复合组织同种异体移植(CTA)中尚未得到系统研究。多次急性排斥反应(AR)对重建移植长期移植物结局的影响尚不清楚。本研究在大鼠后肢同种异体移植模型中系统分析了多次 AR 发作继发的血管病和组织特异性病理变化。LEW 大鼠接受 BN 大鼠后肢移植,并进行如下处理:组 1(Iso):同系移植物。组 2(CsA):环孢素(CsA)qd;组 3(多 AR):仅在观察到 AR 时使用 CsA 和地塞米松。组 1 和组 2 未观察到 AR。组 3 观察到多次 AR,每次 AR 均通过脉冲 CsA +地塞米松治疗完全逆转(临床)。与组 1 和组 2 相比,组 3 动物表现出明显的血管病变,伴有皮肤和肌肉萎缩、成纤维增生基因表达上调和纤维化。此外,同种异体骨硬化、脆弱,容易发生愈合不良和不愈合。有趣的是,血管病是一种晚期发现,而在只有几次 AR 发作后,就可以观察到肌肉萎缩伴巨噬细胞浸润的早期现象。总之,多次 AR 发作导致 CTA 中的血管病和组织特异性病理。这是 CTA 中“复合组织血管病和退行性变(CTVD)”的首个证据。

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