Composite Tissue Vasculopathy and Degeneration Following Multiple Episodes of Acute Rejection in Reconstructive Transplantation

被引:77
作者
Unadkat, J. V. [1 ]
Schneeberger, S. [1 ]
Horibe, E. H. [1 ]
Goldbach, C. [2 ]
Solari, M. G. [1 ]
Washington, K. M. [1 ]
Gorantla, V. S. [1 ]
Cooper, G. M. [3 ]
Thomson, A. W. [4 ]
Lee, W. P. Andrew [1 ]
机构
[1] Univ Pittsburgh, Med Ctr, Div Plast Surg, Pittsburgh, PA 15260 USA
[2] Univ Pittsburgh, Ctr Biol Imaging, Pittsburgh, PA USA
[3] Univ Pittsburgh, Dept Surg, Pittsburgh, PA USA
[4] Univ Pittsburgh, Sch Med, Starzl Transplantat Inst, Pittsburgh, PA USA
关键词
Composite tissue allograft; composite tissue transplantation; chronic allograft dysfunction; chronic allograft rejection; chronic graft deterioration; chronic rejection; hand transplant; graft fibrosis; graft vessel disease; face transplantation; ALLOGRAFT SURVIVAL; T-CELLS; IMPACT; OSTEOPETROSIS; CYCLOSPORINE; PATHOGENESIS; MECHANISMS; KIDNEY; HAND; RATS;
D O I
10.1111/j.1600-6143.2009.02941.x
中图分类号
R61 [外科手术学];
学科分类号
摘要
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 inGroups 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.
引用
收藏
页码:251 / 261
页数:11
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