Dalhousie University, Department of Anaesthesia , 10 West Victoria, 1276 South Park St., Halifax, Nova Scotia, B3H 2Y9 , Canada +1 902 473 2331 ; +1 902 423 9454 ;
Expert Opin Drug Discov. 2014 May;9(5):523-31. doi: 10.1517/17460441.2014.905538. Epub 2014 Apr 3.
Sepsis is the dysregulated systemic immune response to an infection. Experimental and clinical research provided detailed insight into the pathophysiology of the disease, but no pathway explored, so far, has been exploited to deliver effective therapies with regard to significant outcome improvement. Increasing incidence and high mortality of sepsis require novel approaches for the development of anti-sepsis drugs.
Since accurate assessment of the patient's condition in sepsis is the basis for the success of novel anti-sepsis drugs, the authors first review briefly biomarkers for improved diagnostics in sepsis. The authors then discuss specific pharmacological approaches with a focus on immune modulation, for example, Toll-like receptor 4 inhibition and modulation of the endocannabinoid system. The authors also cover iron chelation and uncoupling of the nitric oxide pathway.
The failure of anti-sepsis treatments in the past is most likely related to wrong timing of the drugs due to missing reliable biomarkers to assess the condition of the patients. The authors believe that the development of anti-sepsis drugs using time-critical ('vertical') and continuous ('horizontal') approaches may provide the answer for future novel therapeutics.
败血症是机体对感染的失调性全身免疫反应。实验和临床研究为该疾病的病理生理学提供了详细的见解,但迄今为止,还没有探索出任何途径来提供有效的治疗方法,以显著改善预后。败血症的发病率不断上升和死亡率居高不下,需要开发新型抗败血症药物的新方法。
由于败血症患者病情的准确评估是新型抗败血症药物成功的基础,作者首先简要回顾了用于改善败血症诊断的生物标志物。然后,作者讨论了具有特定药理学作用的方法,重点是免疫调节,例如 Toll 样受体 4 抑制和内源性大麻素系统的调节。作者还介绍了铁螯合和一氧化氮途径解偶联。
过去抗败血症治疗的失败很可能与药物的时机错误有关,因为缺乏可靠的生物标志物来评估患者的病情。作者认为,使用时间关键(“垂直”)和连续(“水平”)方法开发抗败血症药物可能为未来的新型治疗方法提供答案。