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The histopathological changes associated with allograft rejection and drug toxicity in renal transplant recipients maintained on FK506: Clinical significance and comparison with cyclosporine

机译:FK506维持与肾移植受者同种异体移植排斥和药物毒性有关的组织病理学变化:临床意义和与环孢素的比较

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摘要

The histopathological changes in 51 renal allograft biopsies from patients immunosuppressed with FK506 were compared with those seen in 30 needle biopsies obtained from patients on cyclosporine. The frequency and severity of rejection episodes were similar in both groups. Tubular vacuolation and myocyte vacuolation were found to be useful morphological markers to monitor short-term drug toxicity associated with both drugs. Long-term administration of FK506 led to striped interstitial fibrosis and arteriolar hyalinosis, similar to that previously documented for cyclosporine. One case each of hemolytic uremic syndrome and necrotizing arteriopathy was noted in patients receiving FK506. FK506 and cyclosporine are structurally unrelated compounds; hence the parallelism observed in their nephrotoxicity profile suggests that the interactions of these drugs with renal tissue involves the operation of two different initial signal-transducing mechanisms, ultimately activating the same final metabolic pathways.
机译:比较了用FK506免疫抑制的患者的51例肾脏同种异体移植活检的组织病理学变化与用环孢菌素患者进行的30例活检的结果。两组的排斥反应发作频率和严重程度相似。发现管状空泡化和肌细胞空泡化是监测与这两种药物相关的短期药物毒性的有用的形态学标记。长期服用FK506导致条纹状间质纤维化和小动脉透明质化,类似于先前报道的环孢素。接受FK506的患者中分别出现1例溶血性尿毒症综合征和坏死性动脉病。 FK506和环孢菌素是结构上无关的化合物;因此,在其肾毒性谱图中观察到的平行性表明,这些药物与肾组织的相互作用涉及两种不同的初始信号传导机制的运作,最终激活了相同的最终代谢途径。

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