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西尼莫德用于治疗继发进展型多发性硬化症。

Siponimod to treat secondary progressive multiple sclerosis.

作者信息

Gajofatto A, Turatti M

机构信息

Department of Neuroscience, Biomedicine and Movement Sciences, University of Verona, Verona, Italy; Unit of Neurology, Borgo Roma Hospital, Azienda Ospedaliera Universitaria Integrata Verona, Verona, Italy.

Unit of Neurology, Borgo Roma Hospital, Azienda Ospedaliera Universitaria Integrata Verona, Verona, Italy.

出版信息

Drugs Today (Barc). 2020 Jan;56(1):37-46. doi: 10.1358/dot.2020.56.1.3091905.

Abstract

Siponimod fumarate (BAF-312) is a synthetic sphingosine 1- phosphate (S1P) receptor modulator, which exerts immunomodulating effects mediated by B- and T-cell sequestration in secondary lymphoid organs. S1P receptor modulators have consistently shown a significant benefit on relapse rate and other measures of disease activity in patients with relapsing multiple sclerosis (MS), compared with both placebo and active comparator. However, most clinical trials of S1P receptor modulators--as well as other therapies for MS--lack evidence of a significant benefit on disability progression. A phase III trial of siponimod for secondary progressive MS showed a significant effect of the active drug compared with placebo on reduction of disability progression. Siponimod exhibits selective affinity for types 1 and 5 S1P receptors, indicating a possible lower risk of bradycardia and vasoconstriction compared with modulators with type 3 S1P receptor affinity. Current evidence supporting siponimod efficacy for secondary progressive MS is reviewed in the present article.

摘要

富马酸西普尼莫德(BAF-312)是一种合成的1-磷酸鞘氨醇(S1P)受体调节剂,它通过将B细胞和T细胞隔离在次级淋巴器官中发挥免疫调节作用。与安慰剂和活性对照药相比,S1P受体调节剂在复发型多发性硬化症(MS)患者的复发率和其他疾病活动指标方面始终显示出显著益处。然而,大多数S1P受体调节剂的临床试验以及其他MS治疗方法都缺乏对残疾进展有显著益处的证据。一项西普尼莫德治疗继发进展型MS的III期试验表明,与安慰剂相比,活性药物在降低残疾进展方面有显著效果。西普尼莫德对1型和5型S1P受体表现出选择性亲和力,这表明与具有3型S1P受体亲和力的调节剂相比,其心动过缓和血管收缩风险可能更低。本文综述了支持西普尼莫德治疗继发进展型MS疗效的现有证据。

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