Alghamdi Amani, Hussain Syed Danish, Wani Kaiser, Sabico Shaun, Alnaami Abdullah M, Amer Osama Emam, Al-Daghri Nasser M
Biochemistry Department, College of Science, King Saud University, Riyadh, Saudi Arabia.
Immun Inflamm Dis. 2025 Apr;13(4):e70194. doi: 10.1002/iid3.70194.
This longitudinal study aimed to assess the impact of COVID-19 vaccination on cytokine profile.
A total of 84 Saudi subjects (57.1% females) with mean age of 27.2 ± 12.3 participated in this longitudinal study. Anthropometric data and fasting blood samples were obtained at baseline and after final vaccination, with an average follow-up duration of 14.1 ± 3.6 months for adolescents and 13.3 ± 3.0 months for adults, calculated from the first dose of vaccination. Assessment of cytokine profiles was done using commercially available assays.
After follow-up, a significant increase in weight and body mass index was observed overall (p = 0.003 and p = 0.002, respectively). Postvaccination, significant increases were observed in several cytokines, including basic fibroblast growth factor 2 (p < 0.001), interferon gamma (IFNγ) (p = 0.005), interleukin-1 beta (IL1β) (p < 0.001), IL4 (p < 0.001), IL6 (p = 0.003), IL7 (p = 0.001), IL17E (p < 0.001), monocyte chemoattractant protein-1 (MCP1) (p = 0.03), MCP3 (p = 0.001), tumor necrosis factor alpha (TNFα) (p < 0.001), and VEGFA (p < 0.001). A significant reduction was observed only in macrophage colony-stimulating factor (p < 0.001). When adjusted for age, epidermal growth factor (EGF), IL4, IL6, MCP3, TNFα, and vascular endothelial growth factor (VEGFA) remained statistically significant. Gender-based analysis revealed that men experienced greater increases in IL6 (p = 0.008), IL4 (p = 0.04), and TNFα (p = 0.015) compared to women. Age-based analysis showed that older participants had more pronounced increases in EGF (p = 0.011), IL6 (p = 0.029), MCP1 (p = 0.042), and TNFα (p = 0.017), while younger participants had a greater increase in VEGFA (p = 0.025).
The findings of this study indicated that COVID-19 vaccination resulted in an increase in cytokine levels, which signifies the persistence of the humoral immune response to messenger RNA (mRNA) vaccines. This effect may be attributed to the persistent production of spike protein and highly inflammatory nature of mRNA-lipid nanoparticle. Additionally, the results suggested differences in cytokine levels based on gender and age. Notably, the cytokine profile remains favorably altered in young adults who received mRNA vaccinations, even after 1 year.
本纵向研究旨在评估新冠病毒疫苗接种对细胞因子谱的影响。
共有84名沙特受试者(57.1%为女性)参与了这项纵向研究,平均年龄为27.2±12.3岁。在基线和最终接种疫苗后获取人体测量数据和空腹血样,青少年从第一剂疫苗接种开始计算的平均随访时间为14.1±3.6个月,成年人则为13.3±3.0个月。使用市售检测方法评估细胞因子谱。
随访后,总体体重和体重指数显著增加(分别为p = 0.003和p = 0.002)。接种疫苗后,几种细胞因子显著增加,包括碱性成纤维细胞生长因子2(p < 0.001)、干扰素γ(IFNγ)(p = 0.005)、白细胞介素-1β(IL1β)(p < 0.001)、IL4(p < 0.001)、IL6(p = 0.003)、IL7(p = 0.001)、IL17E(p < 0.001)、单核细胞趋化蛋白-1(MCP1)(p = 0.03)、MCP3(p = 0.001)、肿瘤坏死因子α(TNFα)(p < 0.001)和VEGFA(p < 0.001)。仅巨噬细胞集落刺激因子显著降低(p < 0.001)。在对年龄进行调整后,表皮生长因子(EGF)、IL4、IL6、MCP3、TNFα和血管内皮生长因子(VEGFA)仍具有统计学意义。基于性别的分析显示,与女性相比,男性的IL6(p = 0.008)、IL4(p = 0.04)和TNFα(p = 0.015)增加幅度更大。基于年龄的分析表明,年龄较大的参与者的EGF(p = 0.011)、IL6(p = 0.029)、MCP1(p = 0.042)和TNFα(p = 0.017)增加更为明显,而年龄较小的参与者的VEGFA增加幅度更大(p = 0.025)。
本研究结果表明,新冠病毒疫苗接种导致细胞因子水平升高,这表明对信使核糖核酸(mRNA)疫苗的体液免疫反应持续存在。这种效应可能归因于刺突蛋白的持续产生以及mRNA-脂质纳米颗粒的高度炎症性质。此外,结果表明细胞因子水平存在基于性别和年龄的差异。值得注意的是,即使在1年后,接受mRNA疫苗接种的年轻人的细胞因子谱仍保持良好改变。