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FTY720与环孢素联合使用——皮肤同种异体移植存活及肾功能分析

FTY720 in combination with cyclosporine--an analysis of skin allograft survival and renal function.

作者信息

Silva Francieli Ruiz, Silva Lea Bueno Lucas, Cury Patricia Maluf, Burdmann Emmanuel Almeida, Bueno Valquiria

机构信息

UNESP, Ibilce, São Jose do Rio Preto, SP, Brazil.

出版信息

Int Immunopharmacol. 2006 Dec 20;6(13-14):1911-8. doi: 10.1016/j.intimp.2006.07.014. Epub 2006 Aug 14.

Abstract

Acute and chronic nephrotoxicity caused by CsA continuous administration impair kidney allograft survival. Several clinical and experimental protocols have shown benefits to the kidney after decreasing CsA dose, withdrawing the drug or delaying its introduction after transplantation. FTY720 is a new compound that has immunosuppressive characteristics and increase allograft survival in animal models without causing the side effects of calcineurin inhibitors (CNIs). FTY720 described mechanism of action that consists to alter the lymphocyte migration pattern without impairment of the immune system response against pathogens. In our mice model, FTY720 administered alone or in combination with CsA during 21 days increased skin allograft survival in a fully mismatched strain combination and did not cause significant changes in renal function. Moreover, renal structure was normal in all groups suggesting that at low doses (10 mg/kg/day) CsA can be associated during short-term period to other immunosuppressive drugs, i.e. FTY720 without affecting the kidney. Combination of immunosuppressive compounds with FTY720 and/or delayed introduction of low cyclosporine dose could prevent graft rejection and avoid nephrotoxicity.

摘要

环孢素A持续给药引起的急慢性肾毒性会损害肾移植的存活。多项临床和实验方案表明,降低环孢素A剂量、停药或在移植后延迟使用该药物对肾脏有益。FTY720是一种具有免疫抑制特性的新化合物,可提高动物模型中的移植存活率,且不会引起钙调神经磷酸酶抑制剂(CNIs)的副作用。FTY720的作用机制是改变淋巴细胞迁移模式,而不损害免疫系统对病原体的反应。在我们的小鼠模型中,单独或与环孢素A联合使用21天的FTY720可提高完全不匹配品系组合中的皮肤移植存活率,且不会引起肾功能的显著变化。此外,所有组的肾脏结构均正常,这表明低剂量(10毫克/千克/天)的环孢素A在短期内可与其他免疫抑制药物(即FTY720)联合使用,而不会影响肾脏。免疫抑制化合物与FTY720联合使用和/或延迟引入低剂量环孢素可预防移植排斥并避免肾毒性。

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