Porta Miquel, Pumarega José, Aguilar Ruth, Prieto-Merino David, Campi Laura, Rius Cristina, Villar-García Judit, Vidal Marta, Jimenez Alfons, Peña Antonio, Muñoz Miguel-Ángel, Trasande Leonardo, Bolúmar Francisco, Moncunill Gemma, Gasull Magda, Dobaño Carlota
School of Medicine, Universitat Autònoma de Barcelona, Barcelona, Spain.
Hospital del Mar Research Institute (IMIM), Barcelona, Spain.
Front Public Health. 2025 Aug 20;13:1548456. doi: 10.3389/fpubh.2025.1548456. eCollection 2025.
From a public health perspective it is remarkable that there are yet no longitudinal studies in the general population investigating the influence of the basal immune state, measured before the pandemic, on the risk of SARS-CoV-2 infection and COVID-19.
To investigate the specific and combined effects of personal levels of cytokines and immunoglobulins-measured in individuals' blood 4 years before the pandemic-on the risk of SARS-CoV-2 infection and COVID-19 in a general population.
We conducted a prospective cohort study in 240 individuals from the general population of Barcelona. Thirty cytokines and 31 immunoglobulins were quantified in prepandemic serum samples (collected in 2016-17) by high-throughput multiplex quantitative suspension array technology.
Higher concentrations in 2016-17 of IL-8 and TNF- significantly decreased the risk of SARS-CoV-2 seropositivity in 2020-21, whereas higher concentrations of MIP-1α were a risk factor for seropositivity. Most cytokines in mixtures with IL-8, MIP-1α, TNF-α or G-CSF were associated with SARS-CoV-2 seropositivity (all OR ≥2.0 or OR≤0.4 and < 0.05). The five individual isotype-antigen pairs more clearly associated with seropositivity were: protectively, IgG to CMV pp150, IgG to CMV pp65, and IgG to N OC43; and, increasing risk of seropositivity, IgM to CMV pp65 and IgM to EBV EA-D. The four cytokines most consistently associated with the risk of COVID-19 were also G-CSF, IL-8, TNF-, and MIP-1α. The four isotype-antigen pairs more strongly associated with risk of COVID-19 (all protective) were IgA to CMV pp65 and N 229E, and IgG to EBV EAD and VCAp18.
The unique longitudinal design of this study, with measurements before and during the pandemic in a general population, provides novel knowledge on the protective and detrimental effects of specific individual cytokines and immunoglobulins, and their mixtures, on the risk of SARS-CoV-2 seropositivity and COVID-19. If confirmed, findings would be significantly relevant for medicine and public health.
从公共卫生角度来看,值得注意的是,目前尚未有针对普通人群的纵向研究,探讨大流行前测量的基础免疫状态对SARS-CoV-2感染风险和新冠肺炎的影响。
研究在大流行前4年测量的个体血液中细胞因子和免疫球蛋白水平对普通人群中SARS-CoV-2感染风险和新冠肺炎的单独及联合影响。
我们对来自巴塞罗那普通人群的240名个体进行了一项前瞻性队列研究。通过高通量多重定量悬浮阵列技术,对大流行前血清样本(2016 - 2017年采集)中的30种细胞因子和31种免疫球蛋白进行了定量分析。
2016 - 年IL-8和TNF-的较高浓度显著降低了2020 - 2021年SARS-CoV-2血清学阳性的风险,而MIP-1α的较高浓度是血清学阳性的一个风险因素。与IL-8、MIP-1α、TNF-α或G-CSF混合的大多数细胞因子与SARS-CoV-2血清学阳性相关(所有OR≥2.0或OR≤0.4且<0.05)。与血清学阳性更明显相关的五个个体同种型-抗原对分别是:具有保护作用的,针对巨细胞病毒pp150的IgG、针对巨细胞病毒pp65的IgG和针对N OC43的IgG;以及增加血清学阳性风险的,针对巨细胞病毒pp65的IgM和针对EBV EA-D的IgM。与新冠肺炎风险最一致相关的四种细胞因子也是G-CSF、IL-8、TNF-和MIP-1α。与新冠肺炎风险更强烈相关的四个同种型-抗原对(均具有保护作用)分别是针对巨细胞病毒pp65和N 229E 的IgA,以及针对EBV EAD和VCAp18的IgG。
本研究独特的纵向设计,在普通人群中对大流行前和大流行期间进行了测量,提供了关于特定个体细胞因子和免疫球蛋白及其混合物对SARS-CoV-2血清学阳性风险和新冠肺炎的保护和有害作用的新知识。如果得到证实,这些发现将对医学和公共卫生具有重大意义。