COVID-19 大流行期间通过 SARS-CoV-2 主动免疫的年轻患者体内促炎和抗炎细胞因子的平衡情况

Yulia A. Li, M. N. Dmitrachenko, E. V. Markelova, I. B. Korolev, M. P. Kostinov, L. I. Bondar
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引用次数: 0

摘要

2019 年,COVID-19 大流行开始并改变了世界。冠状病毒 SARS-CoV-2 在全球造成了大范围的疾病和死亡。在这方面,接种疫苗成为产生群体免疫力的最重要工具。我们的研究分析了接种 COVID-19 疫苗前后年轻患者血清中促炎和抗炎细胞因子以及 SARS-CoV-2 抗体的动态变化。研究小组包括 76 名年轻男性。静脉血清中的 IL-1β、IL-4、IL-6、IL-8、IL-10、IL-17、IFNγ、TNFα 以及 COVID-19 的 IgM 和 IgG 抗体的测定采用新西伯利亚 Vector-Best 公司的检测系统,通过 ELISA 方法进行了两次。第一次血样检测在接种疫苗前进行,第二次在接种 COVID-19 疫苗 1 个月后进行。结果使用 STATISTICA 8.0 进行处理。疫苗接种后对接种者进行了 6 个月的监测。接种前的指数水平:IL-1β(5.6 pg/ml(Q₂₅-Q₇₅ = 3.1-14.2);IL-4(1.02 pg/ml(Q₂₅-Q₇₅ = 0.75-1.28);IL-6(27.8 pg/ml(Q₂₅-Q₇₅ = 7.1-59.9);IL-8(29.9 pg/ml(Q₂₅-Q₇₅ = 19.51-32.14);IL-10(4.47 pg/ml (Q₂₅-Q₇₅ = 1.84-14.75);IL-17(7.33 pg/ml (Q₂₅-Q₇₅ = 6.82-8.58);IFNγ(0.7 pg/ml (Q₂₅-Q₇₅ = 0.4-0.9);TNFα(3.9 pg/ml (Q₂₅-Q₇₅ = 2.2-6.4)。接种疫苗后的指数水平:IL-1β(1.6 pg/ml (Q₂₅-Q₇₅ = 1.4- 2.2);IL-4(0.84 pg/ml (Q₂₅-Q₇₅ = 0.59-1.12);IL-6(1.2 pg/ml (Q₂₅-Q₇₅ = 0.6-1.7);IL-8(10.1 pg/ml (Q₂₅-Q₇₅ = 3.8-28.9); IL-10 (5.84 pg/ml (Q₂₅-Q₇₅ = 1-9.99); IFNγ (0.6 pg /ml (Q₂₅-Q₇₅ = 0.3-0.8); TNFα (0.6 pg/ml (Q₂₅-Q₇₅ = 0.3-1.9).在接种 SARS-CoV-2 疫苗前后,细胞因子水平的分布不同,呈下降趋势,但尽管如此,许多细胞因子之间仍存在很强的相关性,这表明接种疫苗后免疫系统的紧张度增加。在计算促炎细胞因子和抗炎细胞因子的比率时,发现其下降了两倍,这反映了接种疫苗后促炎细胞因子水平的下降。在 98% 的受试者中,COVID-19 的 IgG 抗体水平超过了保护水平:超过了 14 倍。进一步研究 SARS-CoV-2 疫苗接种对先天性免疫的影响将使我们能够重新考虑目前的疫苗接种策略,并确定预防 COVID-19 的最佳方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Balance of pro- and anti-inflammatory cytokines in young patients who passed active Immunization against SARS-CoV-2 during the COVID-19 Pandemic
In 2019, the COVID-19 pandemic began and changed the world. Coronavirus SARS-CoV-2 has caused widespread illness and death around the world. In this regard, vaccination become the most important tool for creating herd immunity. Our study analyzed the dynamics of pro- and anti-inflammatory cytokines and antibodies to SARS-CoV-2 in the blood serum of young patients before and after vaccination against COVID-19. The study group included 76 young men. Determination of IL-1β, IL-4, IL-6, IL-8, IL-10, IL-17, IFNγ, TNFα and IgM and IgG antibodies to COVID-19 in venous blood sera was carried out twice, by ELISA using the test systems of Vector-Best Company, Novosibirsk. The first blood samples were carried out before vaccination, the second — 1 month after vaccination against COVID-19. The results were processed using STATISTICA 8.0. The vaccinated people were monitored for 6 months after vaccination. Levels of indices before vaccination: IL-1β (5.6 pg/ml (Q₂₅–Q₇₅ = 3.1–14.2); IL-4 (1.02 pg/ml (Q₂₅–Q₇₅ = 0.75–1.28); IL-6 (27.8 pg/ml (Q₂₅–Q₇₅ = 7.1–59.9); IL-8 (29.9 pg/ml (Q₂₅–Q₇₅ = 19.51–32.14); IL-10 (4.47 pg/ ml (Q₂₅–Q₇₅ = 1.84–14.75); IL-17 (7.33 pg/ml (Q₂₅–Q₇₅ = 6.82–8.58); IFNγ (0.7 pg/ml (Q₂₅–Q₇₅ = 0.4–0.9); TNFα (3.9 pg/ml (Q₂₅–Q₇₅ = 2.2–6.4). Levels of indices after vaccination: IL-1β (1.6 pg/ml (Q₂₅–Q₇₅ = 1.4- 2.2); IL-4 (0.84 pg/ml (Q₂₅–Q₇₅ = 0.59–1.12); IL-6 (1.2 pg/ml (Q₂₅–Q₇₅ = 0.6–1.7); IL-8 (10.1 pg/ml (Q₂₅–Q₇₅ = 3.8–28.9); IL-10 (5.84 pg/ml (Q₂₅–Q₇₅ = 1–9.99); IFNγ (0.6 pg /ml (Q₂₅–Q₇₅ = 0.3–0.8); TNFα (0.6 pg/ml (Q₂₅–Q₇₅ = 0.3–1.9). Both before and after vaccination against SARS-CoV-2, different distributions of cytokine levels were identified with a downward trend, but despite this, strong correlations were observed between many of them, which indicates an increase in the tension of the immune system in response to vaccination. When calculating the ratio of pro- and anti-inflammatory cytokines, its two-fold decrease was revealed, which reflects a decrease in the levels of pro-inflammatory cytokines after vaccination. The level of IgG antibodies to COVID-19 exceeded the protective level: more than 14 times in 98% of subjects. Further research into the impact of SARS-CoV-2 vaccination on innate immunity will allow us to reconsider the current vaccination strategy and determine the best approach to preventing COVID-19.
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