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大鼠心脏移植。I. 组织相容性差异对移植动脉硬化的影响。

Cardiac transplantation in the rat. I. The effect of histocompatibility differences on graft arteriosclerosis.

作者信息

Cramer D V, Qian S Q, Harnaha J, Chapman F A, Estes L W, Starzl T E, Makowka L

机构信息

Department of Pathology, University of Pittsburgh School of Medicine, Pennsylvania 15261.

出版信息

Transplantation. 1989 Mar;47(3):414-9. doi: 10.1097/00007890-198903000-00002.

Abstract

The development of arteriosclerosis is the most serious and common complication in long-term survivors of cardiac transplantation. We have used a variety of inbred rat strains with selected histocompatibility differences to examine the influence of prolonged, mild rejection reactions on the development of pathological changes in long-term cardiac allografts. Heterotopic cardiac allografts were exchanged between rat strains that differed for MHC class I (RT1.A and/or RT1.E) antigens or groups of minor, non-MHC antigens in MHC-compatible congenic combinations. Our results demonstrate that in strain combinations in which the allograft reaction is mild and prolonged, the donor hearts exhibit pathological changes that include a diffuse, interstitial myocardial fibrosis, perivascular fibrosis, and intimal proliferation in arteries of the graft myocardium. The lesions were less prominent in animals with more active rejection and infrequent in strains that differ for class I histocompatibility antigens or syngeneic controls. These results suggest that the comparable pathological changes seen in long-term human cardiac survivors may reflect low-level, persistent allograft reactions rather than factors associated with graft anoxia or effects of immunotherapy to prevent graft rejection.

摘要

动脉硬化的发展是心脏移植长期存活者中最严重且常见的并发症。我们使用了多种具有特定组织相容性差异的近交系大鼠品系,以研究长期、轻度排斥反应对长期心脏同种异体移植病理变化发展的影响。在 MHC 相容的同基因组合中,于不同 MHC I 类(RT1.A 和/或 RT1.E)抗原或次要的非 MHC 抗原组不同的大鼠品系之间交换异位心脏同种异体移植。我们的结果表明,在同种异体移植反应轻微且持续时间长的品系组合中,供体心脏呈现出病理变化,包括弥漫性间质心肌纤维化、血管周围纤维化以及移植心肌动脉内膜增生。在排斥反应更活跃的动物中,病变不太明显,而在 I 类组织相容性抗原不同的品系或同基因对照中则很少见。这些结果表明,在长期存活的人类心脏移植受者中观察到的类似病理变化可能反映了低水平的持续性同种异体移植反应,而非与移植缺氧相关的因素或预防移植排斥的免疫治疗效果。

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