肾移植后免疫抑制疗法与肠道微生物群相互干扰的最新进展

Maurizio Salvadori, G. Rosso
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引用次数: 0

摘要

肾移植后,肠道微生物群通常会发生变化。这主要发生在移植后的第一阶段。抗生素和最主要的免疫抑制剂是主要原因。免疫抑制药物与肠道微生物群之间的关系是双边的。一方面,免疫抑制剂会改变肠道微生物群,往往会造成菌群失调;另一方面,微生物群可能会干扰免疫抑制剂的药代动力学,产生比原药物活性更强或更弱的产物。这些现象会对移植结果和临床后果产生影响,因为排斥、感染、腹泻可能是由菌群失调引起的。皮质类固醇、钙神经蛋白抑制剂(如他克莫司和环孢素)、霉酚酸酯和 mTOR 抑制剂等免疫抑制剂对肠道微生物群的影响是众所周知的。相反,众所周知,肠道微生物群可能会干扰糖皮质激素,而糖皮质激素可能会转化为雄激素。他克莫司可被微生物群转化为一种名为 M1 的产物,其活性比他克莫司低 15 倍。原药霉酚酸酯(mycophenolate mofetil)通常会转化为霉酚酸,根据是否存在产生葡萄糖醛酸酶的微生物,霉酚酸酯可能会转化为非活性产物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Update on the reciprocal interference between immunosuppressive therapy and gut microbiota after kidney transplantation
Gut microbiota is often modified after kidney transplantation. This principally happens in the first period after transplantation. Antibiotics and, most of all, immunosuppressive drugs are the main responsible. The relationship between immunosuppressive drugs and the gut microbiota is bilateral. From one side immunosuppressive drugs modify the gut microbiota, often generating dysbiosis; from the other side microbiota may interfere with the immunosuppressant pharmacokinetics, producing products more or less active with respect to the original drug. These phenomena have influence over the graft outcomes and clinical consequences as rejections, infections, diarrhea may be caused by the dysbiotic condition. Corticosteroids, calcineurin inhibitors such as tacrolimus and cyclosporine, mycophenolate mofetil and mTOR inhibitors are the immunosuppressive drugs whose effect on the gut microbiota is better known. In contrast is well known how the gut microbiota may interfere with glucocorticoids, which may be transformed into androgens. Tacrolimus may be transformed by microbiota into a product called M1 that is 15-fold less active with respect to tacrolimus. The pro-drug mycophenolate mofetil is normally transformed in mycophenolic acid that according the presence or not of microbes producing the enzyme glucuronidase, may be transformed into the inactive product.
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