4.1 Editorial Material

Fine-Tuning S1P Therapeutics

期刊

CHEMISTRY & BIOLOGY
卷 19, 期 9, 页码 1080-1082

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CELL PRESS
DOI: 10.1016/j.chembiol.2012.09.002

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资金

  1. NHLBI NIH HHS [HL89934, HL70694, R01 HL089934, P01 HL070694, R37 HL067330, HL67330, R01 HL067330] Funding Source: Medline

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Sphingosine 1-phosphate receptor-1 (S1P(1)), a novel therapeutic target for multiple sclerosis, regulates lymphocyte trafficking, heart rate, and vascular function. The discovery of NIBR-0213, a competitive antagonist for S1P(1) that inhibits autoimmune inflammation while sparing bradycardia (Quancard et al., in this issue of Chemistry & Biology), suggests that fine-tuning of SIP, modulators may lead to novel immune modulators with better efficacy to adverse events ratio.

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