Department of Internal Diseases and Clinical Pharmacology, Laboratory of Tissue Immunopharmacology, Medical University of Lodz, Lodz, Poland.
Department of Internal Diseases and Clinical Pharmacology, Laboratory of Tissue Immunopharmacology, Medical University of Lodz, Lodz, Poland.
Adv Med Sci. 2023 Sep;68(2):195-201. doi: 10.1016/j.advms.2023.05.001. Epub 2023 May 20.
Interleukin (IL)-33 and its soluble receptor ST2 (sST2) play a crucial role in the immune response. sST2 has been approved by the Food and Drug Administration as a prognostic biomarker of mortality in chronic heart failure patients, however, the role of IL-33 and sST2 in atherosclerotic cardiovascular disease remains unclear. The aim of this study was to measure serum level of IL-33 and sST2 of patients at the onset of acute coronary syndrome (ACS) and 3 months after primary percutaneous revascularization.
Forty patients were divided into ST segment elevation myocardial infarction (STEMI) group, non-ST segment elevation myocardial infarction (NSTEMI) and unstable angina (UA) group. IL-33 and sST2 level were measured with ELISA. Additionally, IL-33 expression in peripheral blood mononuclear cells (PBMCs), was evaluated.
All ACS patients had a significantly lower level of sST2 3 months after ACS as compared to the baseline (p < 0.039). The STEMI patients had higher serum levels of IL-33 at the moment of ACS as compared to 3 months after the event, with an average decrease of 17.87 pg/ml (p < 0.007). Conversely, sST2 serum levels were still high after 3 months following an ACS in STEMI patients. ROC curve demonstrated that increased IL-33 serum level could be STEMI predictor.
The assessment of the baseline and dynamics of changes in IL-33 and sST2 concentrations in patients with ACS may be important for the diagnostic process and may help in understanding of how the immune mechanisms work at the moment of an ACS event.
白细胞介素 (IL)-33 和其可溶性受体 ST2(sST2)在免疫反应中发挥着关键作用。sST2 已被美国食品和药物管理局批准为慢性心力衰竭患者死亡率的预后生物标志物,然而,IL-33 和 sST2 在动脉粥样硬化性心血管疾病中的作用仍不清楚。本研究旨在测量急性冠状动脉综合征 (ACS) 患者发病时和经皮冠状动脉血运重建 3 个月后的血清 IL-33 和 sST2 水平。
40 名患者被分为 ST 段抬高型心肌梗死 (STEMI) 组、非 ST 段抬高型心肌梗死 (NSTEMI) 和不稳定型心绞痛 (UA) 组。采用 ELISA 法测量 IL-33 和 sST2 水平。此外,还评估了外周血单核细胞 (PBMC) 中 IL-33 的表达。
所有 ACS 患者在 ACS 后 3 个月的 sST2 水平明显低于基线(p < 0.039)。STEMI 患者在 ACS 时的血清 IL-33 水平高于事件后 3 个月,平均下降 17.87 pg/ml(p < 0.007)。相反,STEMI 患者在 ACS 后 3 个月,sST2 血清水平仍较高。ROC 曲线表明,血清 IL-33 水平升高可预测 STEMI。
评估 ACS 患者基线和变化过程中 IL-33 和 sST2 浓度的变化可能对诊断过程很重要,并有助于了解免疫机制在 ACS 事件发生时的作用。