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Sex and the single transplanted kidney

机译:性与单肾移植

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Substantial ischemia-reperfusion injury (IRI) to the transplanted kidney occurs in 30% to 50% of transplantation patients who receive the organ from a deceased donor. IRI usually manifests as delayed graft function (DGF) and, in severe cases, results in primary nonfunction. Previous studies, primarily experimental, have demonstrated sex-specific susceptibility to IRI in kidney and other organs. In this issue of the JCI , Aufhauser Jr., Wang, and colleagues further demonstrate the importance of donor and recipient sex in IRI and elucidate the role of estrogen receptors in a murine model. Furthermore, analysis of data from 46,691 renal transplant patients in the United Network for Organ Sharing (UNOS) database revealed that sex affects DGF outcomes in humans. Manipulation of sex-driven molecular pathways offers a fertile opportunity to increase the number of organs available for transplantation and to reduce IRI in kidney and, likely, other organs.
机译:从已故的供者那里获得器官的移植患者中,有30%至50%对移植的肾脏发生实质性缺血再灌注损伤(IRI)。 IRI通常表现为移植物功能延迟(DGF),严重时会导致原发性功能障碍。先前的研究,主要是实验性研究,证明了肾脏和其他器官对IRI的性别特异性敏感性。在本期JCI中,Aufhauser Jr.,Wang和同事进一步证明了IRI中供体和受体性别的重要性,并阐明了雌激素受体在鼠模型中的作用。此外,在美国器官共享网络(UNOS)数据库中对46691例肾移植患者的数据进行的分析表明,性别会影响人类的DGF结局。性别驱动的分子途径的操纵提供了肥沃的机会,可以增加可用于器官移植的器官数量,并减少肾脏以及其他器官的IRI。

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