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一种单选择性鞘氨醇-1-磷酸受体-1激动剂在严格的大鼠心脏移植模型中可预防同种异体移植排斥反应。

A monoselective sphingosine-1-phosphate receptor-1 agonist prevents allograft rejection in a stringent rat heart transplantation model.

作者信息

Pan Shifeng, Mi Yuan, Pally Charles, Beerli Christian, Chen Alice, Guerini Danilo, Hinterding Klaus, Nuesslein-Hildesheim Barbara, Tuntland Tove, Lefebvre Sophie, Liu Yi, Gao Wenqi, Chu Alan, Brinkmann Volker, Bruns Christian, Streiff Markus, Cannet Catherine, Cooke Nigel, Gray Nathanael

机构信息

Genomics Institute of the Novartis Research Foundation, 10675 John Jay Hopkins Drive, San Diego, California 92121, USA.

出版信息

Chem Biol. 2006 Nov;13(11):1227-34. doi: 10.1016/j.chembiol.2006.09.017.

Abstract

FTY720 is an immunomodulator with demonstrated efficacy in a phase II trial of relapsing multiple sclerosis. FTY720-phosphate, the active metabolite generated upon phosphorylation in vivo, acts as a potent agonist on four of the five known sphingosine-1-phosphate (S1P(1)) receptors. AUY954, an aminocarboxylate analog of FTY720, is a low nanomolar, monoselective agonist of the S1P(1) receptor. Due to its selectivity and pharmacokinetic profile, AUY954 is an excellent pharmacological probe of S1P(1)-dependent phenomena. Oral administration of AUY954 induces a profound and reversible reduction of circulating lymphocytes and, in combination with RAD001 (Certican/Everolimus, an mTOR inhibitor), is capable of prolonging the survival of cardiac allografts in a stringent rat transplantation model. This demonstrates that a selective agonist of the S1P(1) receptor is sufficient to achieve efficacy in an animal model of transplantation.

摘要

FTY720是一种免疫调节剂,在复发型多发性硬化症的II期试验中已证明具有疗效。FTY720-磷酸盐是体内磷酸化后产生的活性代谢物,对五种已知的1-磷酸鞘氨醇(S1P(1))受体中的四种起强效激动剂作用。AUY954是FTY720的氨基羧酸盐类似物,是一种低纳摩尔浓度、对S1P(1)受体具有单选择性的激动剂。由于其选择性和药代动力学特性,AUY954是研究依赖S1P(1)的现象的极佳药理学探针。口服AUY954可引起循环淋巴细胞显著且可逆的减少,并且与RAD001(Certican/依维莫司,一种mTOR抑制剂)联合使用时,在严格的大鼠移植模型中能够延长心脏异体移植物的存活时间。这表明S1P(1)受体的选择性激动剂足以在移植动物模型中实现疗效。

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