Department of Traumatology and Acute Critical Medicine, Osaka University Graduate School of Medicine, 2-15 Yamadaoka, Suita, Osaka, 565-0871, Japan.
Department of Clinical Application of Biologics, Osaka University Graduate School of Medicine, Osaka University, 2-15 Yamadaoka, Suita, Osaka, 565-0871, Japan.
Sci Rep. 2018 Sep 18;8(1):13995. doi: 10.1038/s41598-018-32275-8.
Sepsis remains a major cause of death. Cytokines interact closely with each other and play a crucial role in the progression of sepsis. We focussed on the associations of a cytokine network with prognosis and disease severities in sepsis. This retrospective study included 31 patients with sepsis and 13 healthy controls. Blood samples were collected from patients on days 1, 2, 4, 6, 8, 11 and 15 and from healthy controls. Levels of PAI-1, IFN-α, IFN-γ, IL-1β, IL-6, IL-8, IL-12/IL-23p40, IL-17A, TNF-α, MCP-1, IL-4 and IL-10 were measured. SOFA, JAAM DIC and ISTH DIC scores were evaluated at the same times blood samples were taken. Network analysis revealed a network formed by PAI-1, IL-6, IL-8, MCP-1 and IL-10 on days 1, 2 and 4 throughout the acute phase of sepsis. There were positive correlations of each cytokine and the combined score (IL-6 + IL-8 + IL-10 + MCP-1) with the SOFA, JAAM DIC and ISTH DIC scores throughout the acute phase. A Cox proportional hazards model focussed on the acute phase showed that the above combined score was significantly related with patient prognosis, suggesting that the cytokine network of IL-6, IL-8, MCP-1 and IL-10 could play a pivotal role in the acute phase of sepsis.
脓毒症仍然是主要的死亡原因。细胞因子相互密切作用,在脓毒症的进展中起着关键作用。我们专注于细胞因子网络与脓毒症预后和疾病严重程度的关联。这项回顾性研究纳入了 31 名脓毒症患者和 13 名健康对照者。在第 1、2、4、6、8、11 和 15 天采集患者和健康对照者的血液样本。测量 PAI-1、IFN-α、IFN-γ、IL-1β、IL-6、IL-8、IL-12/IL-23p40、IL-17A、TNF-α、MCP-1、IL-4 和 IL-10 的水平。同时采集血液样本评估 SOFA、JAAM DIC 和 ISTH DIC 评分。网络分析显示,在脓毒症急性期的第 1、2 和 4 天,由 PAI-1、IL-6、IL-8、MCP-1 和 IL-10 组成的网络。在整个急性期,每种细胞因子和联合评分(IL-6+IL-8+IL-10+MCP-1)与 SOFA、JAAM DIC 和 ISTH DIC 评分均呈正相关。一个侧重于急性期的 Cox 比例风险模型显示,上述联合评分与患者预后显著相关,表明 IL-6、IL-8、MCP-1 和 IL-10 的细胞因子网络可能在脓毒症急性期发挥关键作用。