Department of Psychiatry, University of Iowa, Iowa City, IA 52242, United States of America.
Department of Sociology, University of Georgia, Athens, GA 30602, United States of America; Center for Family Research, University of Georgia, Athens, GA 30602, United States of America.
J Psychosom Res. 2021 Feb;141:110326. doi: 10.1016/j.jpsychores.2020.110326. Epub 2020 Dec 6.
Smoking is associated with numerous inflammatory and autoimmune conditions. The goal of this study was to examine whether increased expression of G-protein-coupled receptor 15 (GPR15) on helper T cells in smokers could predispose to these conditions through its relationship with inflammatory biomarkers.
We used flow cytometric measurement of GPR15CD3CD4 helper T cells and serum assays for C-reactive protein (CRP) and 17 cytokines drawn from peripheral blood samples from a cohort of n = 62 primarily African American young adults (aged 27-35 years). These variables were examined cross-sectionally in conjunction with serum biomarkers of tobacco (cotinine) and cannabis (tetrahydrocannabinol) use and lifestyle factors potentially impacting immune function in correlational analyses and linear regression models.
Tobacco and cannabis smoking were strongly associated with increased GPR15 expression on helper T cells (p < 0.001), which was in turn was strongly associated with the ratio of pro-inflammatory to anti-inflammatory cytokines (p < 0.001). Mediation analyses indicated increased GPR15 expression accounted for roughly half of the relationship between smoking variables and pro-inflammatory to anti-inflammatory cytokine balance. CRP was not associated with cannabis or tobacco use or GPR15+ expression, but was associated with body mass index (p < 0.001). These relationships persisted after controlling for lifestyle and medical factors impacting immune function.
Increased expression of GPR15 by helper T cells in smokers may mediate some of the relationship between smoking and a pro-inflammatory cytokine milieu. Better understanding of this relationship may help uncover how smoking increases the risk of inflammatory diseases.
吸烟与许多炎症和自身免疫性疾病有关。本研究的目的是通过研究 G 蛋白偶联受体 15(GPR15)在辅助性 T 细胞上的表达增加是否与炎症生物标志物有关,从而导致这些疾病的发生。
我们使用流式细胞术测量了来自 n=62 名主要为非裔美国年轻成年人(年龄 27-35 岁)外周血样本中的 GPR15CD3CD4 辅助性 T 细胞和 C 反应蛋白(CRP)和 17 种细胞因子的血清测定值。在相关分析和线性回归模型中,我们结合血清烟草(可替宁)和大麻(四氢大麻酚)使用以及可能影响免疫功能的生活方式因素,对这些变量进行了横断面检查。
烟草和大麻吸烟与辅助性 T 细胞上 GPR15 表达的增加密切相关(p<0.001),而 GPR15 表达的增加又与促炎细胞因子与抗炎细胞因子的比例密切相关(p<0.001)。中介分析表明,GPR15 表达的增加解释了吸烟变量与促炎细胞因子与抗炎细胞因子平衡之间关系的一半左右。CRP 与大麻或烟草使用或 GPR15+表达无关,但与体重指数(BMI)有关(p<0.001)。这些关系在控制了影响免疫功能的生活方式和医疗因素后仍然存在。
吸烟者辅助性 T 细胞中 GPR15 的表达增加可能介导了吸烟与促炎细胞因子环境之间的部分关系。更好地了解这种关系可能有助于揭示吸烟如何增加炎症性疾病的风险。