Okamura Yoshikazu
Rinsho Byori. 2015 Jan;63(1):62-71.
Sepsis is a systemic inflammatory response syndrome (SIRS) caused by infection, and it is one of the major causes of mortality of critical care patients. Since it has been reported that early, optimal treatment of patients is important to reduce mortality from sepsis, a sepsis marker with a high sensitivity and specificity is required. Presepsin (P-SEP) was discovered as a new marker whose levels elevated specifically in the blood of patients with sepsis in Japan in 2002. Presepsin is a 13-kDa glycoprotein that is a truncated N-terminal fragment of CD14. Since one of the production mechanisms of presepsin is related to the phagocytosis of bacteria, the biological characteristics of presepsin are different from those of other inflammatory markers. Presepsin has three features in comparison with procalcitonin(PCT), C-reactive protein(CRP), and interleukin-6 (IL-6): 1) Presepsin can be detected earlier after the onset of infection; 2) Presepsin is not affected by severe trauma, severe burn, or invasive surgical procedures, which lead to SIRS, more than PCT, CRP, or IL-6; 3) Presepsin levels reflect the clinical condition of septic patients. Although clinical evidence is not sufficient at present, presepsin may be a strong tool for the development of novel treatment strategies for sepsis.
脓毒症是一种由感染引起的全身炎症反应综合征(SIRS),是重症监护患者死亡的主要原因之一。由于已有报道称,对患者进行早期、优化治疗对于降低脓毒症死亡率至关重要,因此需要一种具有高灵敏度和特异性的脓毒症标志物。2002年在日本,可溶性髓系细胞触发受体-1(P-SEP)作为一种新的标志物被发现,其水平在脓毒症患者血液中特异性升高。可溶性髓系细胞触发受体-1是一种13kDa的糖蛋白,是CD14的截短N端片段。由于可溶性髓系细胞触发受体-1的产生机制之一与细菌吞噬作用有关,因此其生物学特性与其他炎症标志物不同。与降钙素原(PCT)、C反应蛋白(CRP)和白细胞介素-6(IL-6)相比,可溶性髓系细胞触发受体-1具有三个特点:1)在感染发生后能更早检测到;2)与PCT、CRP或IL-6相比,可溶性髓系细胞触发受体-1受导致SIRS的严重创伤、严重烧伤或侵入性外科手术的影响更小;3)可溶性髓系细胞触发受体-1水平反映脓毒症患者的临床状况。尽管目前临床证据尚不充分,但可溶性髓系细胞触发受体-1可能是开发脓毒症新型治疗策略的有力工具。