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Orthotopic liver/small bowel transplantation in rats: a microsurgical model inducing tolerance.

机译:大鼠原位肝/小肠移植:诱导耐受的显微外科模型。

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摘要

Liver cirrhosis in patients with short bowel syndrome is successfully treated in humans by simultaneous liver/small bowel transplantation. However, until now, a clinically relevant experimental rat model for this procedure has not existed. We therefore established a protocol that, for the first time in rats, allows the simultaneous transplantation of arterialized liver and small bowel into an orthotopic position. Short-term immunosuppression induced not only allograft acceptance but tolerance (as demonstrated by indicator heart/skin transplantation). The immunosuppressive dose required to achieve this result was dramatically less than that of protocols for successful small bowel transplantation alone. Immunohistochemistry detected a transient rejection crisis before tolerance. During this crisis, apoptotic recipient-type T lymphocytes, mainly CD8+ cells, accumulated in the liver but not in the small bowel allograft. The initiation of T-cell apoptosis is one possible explanation for the specific immunosuppressive effect of the liver allograft, which also supports the simultaneously transplanted small bowel allograft in our model.
机译:短肠综合征患者的肝硬化已通过肝/小肠同时移植在人类中得到成功治疗。但是,到目前为止,还没有针对该程序的临床相关实验大鼠模型。因此,我们建立了一种协议,该协议首次在大鼠中允许将动脉化的肝脏和小肠同时移植到原位。短期免疫抑制不仅诱导同种异体移植接受,而且诱导耐受性(如指示剂心脏/皮肤移植所证明)。获得此结果所需的免疫抑制剂量大大小于仅成功进行小肠移植的方案的免疫抑制剂量。免疫组化检测到耐受之前有短暂的排斥反应。在此危机期间,凋亡的受体型T淋巴细胞(主要是CD8 +细胞)在肝脏中积累,但在小肠同种异体移植物中不积累。 T细胞凋亡的开始是肝脏同种异体移植物特异性免疫抑制作用的一种可能的解释,这也支持我们模型中同时移植的小肠同种异体移植物。

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