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针对免疫介导疾病中的1-磷酸鞘氨醇信号通路:超越多发性硬化症

Targeting Sphingosine-1-Phosphate Signaling in Immune-Mediated Diseases: Beyond Multiple Sclerosis.

作者信息

Pérez-Jeldres Tamara, Alvarez-Lobos Manuel, Rivera-Nieves Jesús

机构信息

Pontificia Universidad Católica de Chile, Santiago, Chile.

Hospital San Borja-Arriarán, Santiago, Chile.

出版信息

Drugs. 2021 Jun;81(9):985-1002. doi: 10.1007/s40265-021-01528-8. Epub 2021 May 13.

Abstract

Sphingosine-1-phosphate (S1P) is a bioactive lipid metabolite that exerts its actions by engaging 5 G-protein-coupled receptors (S1PR1-S1PR5). S1P receptors are involved in several cellular and physiological events, including lymphocyte/hematopoietic cell trafficking. An S1P gradient (low in tissues, high in blood), maintained by synthetic and degradative enzymes, regulates lymphocyte trafficking. Because lymphocytes live long (which is critical for adaptive immunity) and recirculate thousands of times, the S1P-S1PR pathway is involved in the pathogenesis of immune-mediated diseases. The S1PR1 modulators lead to receptor internalization, subsequent ubiquitination, and proteasome degradation, which renders lymphocytes incapable of following the S1P gradient and prevents their access to inflammation sites. These drugs might also block lymphocyte egress from lymph nodes by inhibiting transendothelial migration. Targeting S1PRs as a therapeutic strategy was first employed for multiple sclerosis (MS), and four S1P modulators (fingolimod, siponimod, ozanimod, and ponesimod) are currently approved for its treatment. New S1PR modulators are under clinical development for MS, and their uses are being evaluated to treat other immune-mediated diseases, including inflammatory bowel disease (IBD), rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), and psoriasis. A clinical trial in patients with COVID-19 treated with ozanimod is ongoing. Ozanimod and etrasimod have shown promising results in IBD; while in phase 2 clinical trials, ponesimod has shown improvement in 77% of the patients with psoriasis. Cenerimod and amiselimod have been tested in SLE patients. Fingolimod, etrasimod, and IMMH001 have shown efficacy in RA preclinical studies. Concerns relating to S1PR modulators are leukopenia, anemia, transaminase elevation, macular edema, teratogenicity, pulmonary disorders, infections, and cardiovascular events. Furthermore, S1PR modulators exhibit different pharmacokinetics; a well-established first-dose event associated with S1PR modulators can be mitigated by gradual up-titration. In conclusion, S1P modulators represent a novel and promising therapeutic strategy for immune-mediated diseases.

摘要

鞘氨醇-1-磷酸(S1P)是一种生物活性脂质代谢产物,它通过作用于5种G蛋白偶联受体(S1PR1-S1PR5)来发挥其作用。S1P受体参与多种细胞和生理活动,包括淋巴细胞/造血细胞的转运。由合成酶和降解酶维持的S1P梯度(组织中低,血液中高)调节淋巴细胞的转运。由于淋巴细胞寿命长(这对适应性免疫至关重要)且能循环数千次,S1P-S1PR途径参与免疫介导疾病的发病机制。S1PR1调节剂导致受体内化、随后的泛素化和蛋白酶体降解,这使得淋巴细胞无法跟随S1P梯度并阻止它们进入炎症部位。这些药物还可能通过抑制跨内皮迁移来阻断淋巴细胞从淋巴结的流出。将靶向S1PRs作为一种治疗策略最初用于治疗多发性硬化症(MS),目前有四种S1P调节剂(芬戈莫德、西波莫德、奥扎莫德和波尼莫德)被批准用于其治疗。新型S1PR调节剂正在进行MS的临床试验,并且正在评估它们用于治疗其他免疫介导疾病的用途,包括炎症性肠病(IBD)、类风湿性关节炎(RA)、系统性红斑狼疮(SLE)和银屑病。一项使用奥扎莫德治疗COVID-19患者的临床试验正在进行中。奥扎莫德和依曲莫德在IBD中已显示出有前景的结果;而在2期临床试验中,波尼莫德在77%的银屑病患者中显示出病情改善。塞尼莫德和阿米西莫德已在SLE患者中进行了测试。芬戈莫德、依曲莫德和IMMH001在RA临床前研究中已显示出疗效。与S1PR调节剂相关的担忧包括白细胞减少、贫血、转氨酶升高、黄斑水肿、致畸性、肺部疾病、感染和心血管事件。此外,S1PR调节剂表现出不同的药代动力学;与S1PR调节剂相关的一个公认的首剂事件可以通过逐渐增加剂量来减轻。总之,S1P调节剂代表了一种用于免疫介导疾病的新颖且有前景的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93fa/8217061/504f09f1ed1b/40265_2021_1528_Fig1_HTML.jpg

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