关键词: ARDS Syk barrier function cadherin endothelia fostamatinib inflammation vascular

Mesh : Humans Aminopyridines / therapeutic use Morpholines / therapeutic use Pyrimidines / therapeutic use Syk Kinase / antagonists & inhibitors metabolism Respiratory Distress Syndrome / drug therapy Animals Mice Protein Kinase Inhibitors / therapeutic use Sepsis / drug therapy

来  源:   DOI:10.1016/j.jbc.2024.107517   PDF(Pubmed)

Abstract:
Acute respiratory distress syndrome (ARDS) is a deadly clinical presentation in sepsis, COVID, and other lung disorders where vascular fluid leakage is a severe problem. Recent findings by Shadab et al. in the JBC show that a well-known player in immune function, Syk, also regulates vascular leakage in response to sepsis. An existing FDA-approved inhibitor of Syk, fostamatinib, prevents the vascular leakage and improves survival in a mouse sepsis model, providing promise for ARDS treatment in the clinic.
摘要:
急性呼吸窘迫综合征(ARDS)是败血症的致命临床表现,COVID,和其他肺部疾病,其中血管液体渗漏是一个严重的问题。Shadab等人在JBC中的最新发现表明,在免疫功能方面,Syk,还调节血管渗漏以应对脓毒症。现有的FDA批准的Syk抑制剂,福司替尼,防止血管渗漏,提高小鼠败血症模型的存活率,为临床ARDS治疗提供了希望。
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