接种 Ad26.COV2.S 疫苗后的 CCL20 趋化因子和其他促炎标记物。

Iva Ivanko, Milena Hanžek, Ivana Ćelap, Sandra Margetić, Domagoj Marijančević, Josipa Josipović, Petar Gaćina
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摘要

导言:在 COVID-19 大流行等高度紧张的情况下,疫苗诱导免疫的生物标志物可能特别方便。我们研究的主要目的是确定 Ad26.COV2.S 疫苗接种后 C-C motif ligand 20(CCL20)浓度与更常见的促炎分子的关系,以及它与抗 SARS-CoV-2 抗体浓度的相关性。其次,我们研究了动脉高血压患者和非动脉高血压患者的炎症和免疫特征差异:研究包括接种 Ad26.COV2.S 疫苗的 84 名受试者。调查了接种前、接种后 7 天和 14 天 CCL20、白细胞介素 (IL) 6 和 C 反应蛋白 (CRP) 的浓度,以及接种后 7 天和 14 天抗 SARS-CoV-2 IgG 抗体的浓度。所有指标均采用成熟的实验室方法进行测量:结果:接种疫苗后,CCL20 和 IL-6 的浓度没有明显的统计学变化。结果显示,3个时间点之间的 CRP(P = 0.006)浓度和 2 个时间点之间的 SARS-CoV-2 IgG 抗体(P < 0.001)浓度差异有统计学意义。CCL20 与 IL-6、CRP 或抗 SARS-CoV-2 IgG 抗体的浓度无关。在患有动脉高血压的受试者亚组中,3个时间点之间的 CRP(P = 0.025)浓度差异具有统计学意义:虽然我们的研究结果没有显示接种疫苗后 CCL20 浓度的变化,但可能是由于研究时间框架的原因,进一步调查 SARS-CoV-2 免疫接种后趋化因子的分布情况有助于识别对疫苗的特定反应模式(超优或次优)。
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CCL20 chemokine and other proinflammatory markers after Ad26.COV2.S vaccination.

Introduction: In highly stressed circumstances, such as COVID-19 pandemic, biomarkers of the vaccine-induced immunity could be especially convenient. The main aim of our study was to determine C-C motif ligand 20 (CCL20) concentration after Ad26.COV2.S vaccination in regard to more common proinflammatory molecules and its correlation with anti-SARS-CoV-2 antibody concentration. Secondly, we investigated inflammatory and immunologic profile differences between patients with and without arterial hypertension.

Materials and methods: The study included 84 subjects vaccinated with Ad26.COV2.S vaccine. Concentration of CCL20, interleukin (IL) 6, C-reactive protein (CRP) was investigated before, 7 and 14 days after vaccination and concentration of anti-SARS-CoV-2 IgG antibody 7 and 14 days after vaccination. All the markers were measured by well-established laboratory methods.

Results: There were no statistically significant changes of CCL20 and IL-6 concentration after the vaccination. The obtained results have shown statistically significant differences for CRP (P = 0.006) concentrations between 3 time points and SARS-CoV-2 IgG antibody (P < 0.001) concentrations between 2 time points. CCL20 did not correlate with IL-6, CRP or anti-SARS-CoV-2 IgG antibody concentration. Statistically significant difference for CRP (P = 0.025) concentration between 3 time points was observed in the subgroup of subjects with arterial hypertension.

Conclusions: Although our results did not show changes in CCL20 concentration after the vaccination, possibly due to the study timeframe, further investigations on chemokine profile post SARS-CoV-2 immunization could facilitate the recognition of specific patterns of response (supra- or sub-optimal) to the vaccine.

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