Department of Intensive Care Unit, Guangzhou First People's Hospital, School of Medicine, South China University of Technology, Guangzhou, Guangdong 510180, China.
Department of Radiology, Guangzhou First People's Hospital, School of Medicine, South China University of Technology, Guangzhou, Guangdong 510180, China.
Infect Genet Evol. 2021 Jul;91:104804. doi: 10.1016/j.meegid.2021.104804. Epub 2021 Mar 5.
To explore if SOCS1 is regulated by plasma HDL and its subcomponents HDL2b and HDL3 to affect inflammatory reaction then to influence the severity degree and prognosis of sepsis.
One hundred sepsis patients in ICU and 85 normal control persons from October 2018 to October 2019 in our hospital were enrolled. Adult male C57BL/6 mice were used to establish sepsis model by CLP method. HDL, CRP, and WBC count of human were measured using an auto-analyzer. Plasma HDL, IL-1β, and TNF-α proteins levels of mice were measured with ELISA. Microfluidic chip was used for plasma HDL2b and HDL3 detections. SOCS1 in liver and spleen of mice were measured by qRT-PCR. The relationship between plasma HDL//HDL2b and inflammatory indices/SOCS1 in liver/spleen was analyzed with spearman correlation coefficient method. The sepsis patients/mice were divided into non-survival and survival groups. The sepsis patients were divided into severe and mild sepsis patients based on the SOFA score or divided into high and low score groups according to the APACHE II score. The sepsis mice were divided into high and low score group based on the modified sepsis severity score criterion.
Plasma HDL and HDL2b levels were significantly declined (P < 0.01), while HDL3 was normal in both sepsis patients and mice (P > 0.05). Plasma HDL and HDL2b were negatively associated with the serum CRP concentration and positively correlated with the prognosis and severity in sepsis patients (P < 0.05). Moreover, the downregulated plasma HDL but not HDL2b was negatively related to increased SOCS1 mRNA levels in liver and spleen of mice, which were positively connected with TNF-α and IL-1β protein levels (P < 0.05).
Plasma HDL is downregulated in sepsis, which may facilitate inflammatory reaction then activate the SOCS1 signaling to regulate the severity and affect prognosis of sepsis. The decline of plasma HDL2b content could aggravate the severity and poor prognosis of sepsis through facilitating inflammatory reaction. The plasma HDL3 is not involved in sepsis. The more and further explorations may be needed.
探讨 SOCS1 是否受血浆高密度脂蛋白(HDL)及其亚组分 HDL2b 和 HDL3 的调节,从而影响炎症反应,进而影响脓毒症的严重程度和预后。
选取我院 2018 年 10 月至 2019 年 10 月 ICU 收治的 100 例脓毒症患者和 85 例正常对照者,采用 CLP 法建立成年雄性 C57BL/6 小鼠脓毒症模型。采用自动分析仪检测人血浆 HDL、CRP 和白细胞计数,采用 ELISA 检测小鼠血浆 HDL、IL-1β 和 TNF-α 蛋白水平,采用微流控芯片检测 HDL2b 和 HDL3。采用 qRT-PCR 检测小鼠肝、脾 SOCS1。采用 Spearman 相关系数法分析血浆 HDL//HDL2b 与肝、脾炎症指标/SOCS1 的关系。将脓毒症患者/小鼠分为存活组和死亡组,根据 SOFA 评分将脓毒症患者分为严重脓毒症和轻度脓毒症患者,根据 APACHE II 评分将脓毒症患者分为高分组和低分组,根据改良脓毒症严重程度评分标准将脓毒症小鼠分为高分组和低分组。
脓毒症患者和小鼠的血浆 HDL 和 HDL2b 水平显著降低(P < 0.01),而 HDL3 水平正常(P > 0.05)。脓毒症患者的血浆 HDL 和 HDL2b 与血清 CRP 浓度呈负相关,与脓毒症患者的预后和严重程度呈正相关(P < 0.05)。此外,下调的血浆 HDL 但不是 HDL2b 与小鼠肝、脾中 SOCS1 mRNA 水平的升高呈负相关,而 SOCS1 mRNA 水平与 TNF-α 和 IL-1β 蛋白水平呈正相关(P < 0.05)。
脓毒症患者的血浆 HDL 降低,可能通过促进炎症反应进而激活 SOCS1 信号通路,调节严重程度,影响脓毒症的预后。血浆 HDL2b 含量的降低可能通过促进炎症反应加重脓毒症的严重程度和不良预后。血浆 HDL3 不参与脓毒症,可能需要进一步深入研究。