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Direct-Acting-Antivirals Anti-hepatitis C Virus in Renal Transplant Patients: Relevance of Pharmacologic Interaction

机译:肾移植患者的直效 - 抗病毒抗丙型肝炎病毒:药理学互动的相关性

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Renal transplantation in patients affected by hepatitis C virus (HCV) infection has been a serious problem becauseof the use of immunosuppres-sants. HCV virus may be more aggressive in both the liver and the kidney. Several posttransplantation pathologies are known to be ascribed to the HCV virus.Virus eradication has been historically attempted with interferon (IFN) and ribavirin with poor results. In addition, IFN given posttransplan-tation may cause severe acute rejection.The introduction of direct antiviral agents (DAA) has revolutionized the treatment, and now it is possible to treat renal transplant patients with these agents leading to a HCV-free status in 3 months without the use of IFN.The major problem caused by these agents is their interference with the immunosuppressive agents.The pharmacokinetics of DAA and immunosuppressants often meet the same metabolic pathways and use the same cytochromes or proteic complexes. In some cases, this may lead to high or low immunosuppressant levels with the risk of rejection. In other cases, the DAAs are inter-ested and they may be increase or decrease in a dangerous way. Therefore a strict monitoring is always recommended.
机译:受丙型肝炎病毒(HCV)感染影响的患者的肾移植是一种严重的问题,因为使用免疫奢华术。 HCV病毒在肝脏和肾脏中可能更具侵略性。已知几种后翻透病理学将归因于HCV病毒。历史上历史上已经尝试了干扰素(IFN)和利巴韦林,结果差。此外,IFN给予后横穿率可能导致严重的急性排斥反应。直接抗病毒剂(DAA)的引入已经彻底改变了治疗,现在可以将肾移植患者治疗这些药剂导致3个导致3个导致HCV的地位未使用IFN的月份。这些试剂引起的主要问题是它们对免疫抑制剂的干扰。DAA和免疫抑制剂的药代动力学经常满足相同的代谢途径,并使用相同的细胞变色或蛋白质复合物。在某些情况下,这可能导致具有抑制风险的高或低免疫抑制水平。在其他情况下,DAA是间间的,它们可能以危险的方式增加或减少。因此,始终建议严格的监控。

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