Centre for Human Drug Research, Leiden, Netherlands.
Division of BioTherapeutics, Leiden Academic Center for Drug Research, Leiden University, Leiden, Netherlands.
Front Immunol. 2022 Sep 15;13:968815. doi: 10.3389/fimmu.2022.968815. eCollection 2022.
Currently immunomodulatory compounds are under investigation for use in patients with cardiovascular disease, caused by atherosclerosis. These trials, using recurrent cardiovascular events as endpoint, require enrollment of large patient groups. We investigated the effect of key risk factors for atherosclerosis development, ageing and smoking, on the immune system, with the objective to identify biomarkers differentiating between human populations, and potentially serving as endpoints for future phase 1B trials with immunomodulatory compounds. Blood was collected from young healthy volunteers (aged 18-25 years, n=30), young smokers (18-25 years, n=20), elderly healthy volunteers (>60 years, n=20), heavy smokers (>45 years, 15 packyears, n=11) and patients with stable coronary artery disease (CAD) (>60 years, n=27). Circulating immune cell subsets were characterized by flow cytometry, and collected plasma was evaluated by proteomics (Olink). Clear ageing effects were observed, mostly illustrated by a lower level in CD8 and naïve CD4 and CD8 T cells, with an increase in CD4 and CD8 effector memory T cells in elderly healthy volunteers compared to young healthy volunteers. Heavy smokers showed a more inflammatory cellular phenotype, especially a shift in Th1/Th2 ratio: higher Th1 and lower Th2 percentages compared to young healthy volunteers. A significant decrease in circulating atheroprotective oxLDL-specific IgM was found in patients with CAD compared to young healthy volunteers. Elevated pro-inflammatory and chemotactic proteins TREM1 and CCL11 were observed in elderly volunteers compared to young volunteers. In addition, heavy smokers had an increase in pro-inflammatory cytokine IL-6 and lysosomal protein LAMP3. These data show that ageing and smoking are associated with an inflammatory immunophenotype, and that heavy smokers or aged individuals may serve as potential populations for future clinical trials investigating immunomodulatory drugs targeted for cardiovascular disease.
目前,免疫调节化合物正被研究用于治疗动脉粥样硬化引起的心血管疾病。这些试验以心血管事件复发作为终点,需要招募大量患者。我们研究了动脉粥样硬化发展的关键危险因素,即衰老和吸烟,对免疫系统的影响,旨在确定区分人群的生物标志物,并可能作为未来免疫调节化合物 1B 期临床试验的终点。从年轻健康志愿者(年龄 18-25 岁,n=30)、年轻吸烟者(18-25 岁,n=20)、老年健康志愿者(>60 岁,n=20)、重度吸烟者(>45 岁,15 包年,n=11)和稳定性冠状动脉疾病(CAD)患者(>60 岁,n=27)中采集血液。通过流式细胞术对循环免疫细胞亚群进行了特征描述,并通过蛋白质组学(Olink)评估了收集的血浆。观察到明显的衰老效应,主要表现为 CD8 和幼稚 CD4 和 CD8 T 细胞水平降低,与年轻健康志愿者相比,老年健康志愿者中 CD4 和 CD8 效应记忆 T 细胞增加。重度吸烟者表现出更具炎症性的细胞表型,尤其是 Th1/Th2 比值的变化:与年轻健康志愿者相比,Th1 百分比较高,Th2 百分比较低。与年轻健康志愿者相比,CAD 患者循环中保护性 oxLDL 特异性 IgM 显著减少。与年轻志愿者相比,老年志愿者中观察到促炎和趋化蛋白 TREM1 和 CCL11 升高。此外,重度吸烟者促炎细胞因子 IL-6 和溶酶体蛋白 LAMP3 增加。这些数据表明,衰老和吸烟与炎症免疫表型有关,重度吸烟者或老年人可能作为未来针对心血管疾病的免疫调节药物临床试验的潜在人群。