免疫、脂蛋白组学和炎症反应的纵向研究表明,顺序接种COVID-19疫苗是安全的。

IF 4.8 3区 医学 Q1 GENETICS & HEREDITY
Journal of Molecular Medicine-Jmm Pub Date : 2025-04-01 Epub Date: 2025-03-12 DOI:10.1007/s00109-025-02527-y
Jurissa Lang, Andres Bernal, Julien Wist, Siobhon Egan, Sze How Bong, Oscar Millet, Monique Ryan, Aude-Claire Lee, Drew Hall, Philipp Nitschke, Reika Masuda, Allison Imrie, Elaine Holmes, Jeremy Nicholson, Ruey Leng Loo
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引用次数: 0

摘要

COVID-19疫苗对于减少SARS-CoV-2传播和严重健康后果至关重要。尽管广泛使用,但它们对人体代谢的长期系统性影响仍未充分了解。这项纵向研究旨在评估33名接受2至4剂COVID-19疫苗的个体的IgG反应、34种细胞因子、112种脂蛋白和21种低分子量代谢物。在每次接种疫苗后的前16天以及首次接种疫苗后的480天内,代谢谱的变化与基线(接种前)进行了比较。此外,将接种疫苗的参与者的代谢谱与未接种疫苗且未暴露于SARS-CoV-2感染的个体(对照组)和SARS-CoV-2病例的参考队列进行比较。首次给药后78.8% (N = 26)的受试者出现IgG阳性反应,后续给药后达到100%。最常见的副作用是注射部位的局部疼痛和“流感样”症状,约50%的参与者报告了这一症状。系统性副作用,如淋巴结痛、疲劳和脑雾,均有报道,但与IgG反应无显著相关性。细胞因子IP10 (CXCL10)和谷氨酸在第三次疫苗剂量前后发生短暂的时间变化。与参考队列相比,497例(95.0%)接种疫苗的样本与对照组相似,而其余26例既往感染暴露的样本与轻度SARS-CooV-2感染病例相似。总之,COVID-19疫苗接种不会引起炎症和代谢反应的持久变化,也不会引起类似于SARS-CoV-2轻度感染病例的变化。这支持了疫苗的代谢安全性,并有助于提高疫苗的信心。关键信息:接种疫苗后480天炎症/代谢标志物变化最小。IP10 (CXCL10)和谷氨酸在第三次给药前后短暂升高。疫苗接种后IgG反应没有像SARS-CoV-2病例那样改变代谢谱。我们的研究结果为重复接种COVID-19疫苗的安全性提供了见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Longitudinal study on immunologic, lipoproteomic, and inflammatory responses indicates the safety of sequential COVID-19 vaccination.

COVID-19 vaccines are crucial in reducing SARS-CoV-2 transmission and severe health outcomes. Despite widespread administration, their long-term systemic effects on human metabolism remain inadequately understood. This longitudinal study aims to evaluate IgG responses, 34 cytokines, 112 lipoproteins, and 21 low-molecular-weight metabolites in 33 individuals receiving two to four COVID-19 vaccine doses. Changes in metabolic profiles for the first 16 days post each dose of vaccine, and up to 480 days post-initial dose, were compared to baseline (before vaccination). Additionally, metabolic profiles of vaccinated participants were compared to a reference cohort of unvaccinated individuals without prior exposure to SARS-CoV-2 infection (controls) and SARS-CoV-2 cases. Positive IgG responses were observed in 78.8% (N = 26) of participants after the first dose, reaching 100% with subsequent doses. The most common side effects were localized pain at the injection site and "flu-like" symptoms, reported by > 50% of participants. Systemic side effects, e.g., sore lymph nodes, fatigue, and brain fog, were reported but showed no significant correlations to IgG responses. Transient temporal changes were observed for cytokine IP10 (CXCL10) and glutamic acid around the third vaccine dose. Compared to the reference cohort, 497 vaccinated samples (95.0%) had profiles similar to the controls, while the remaining 26 samples with prior infection exposures were similar to mild cases of SARS-CooV-2 infection. In conclusion, COVID-19 vaccination did not induce lasting changes in inflammatory and metabolic responses, nor did it induce changes similar to mild cases of SARS-CoV-2 infection. This supports the metabolic safety of the vaccine and contributes to increased vaccine confidence. KEY MESSAGES: Minimal changes in inflammatory/metabolic markers up to 480 days post-vaccination. Transient increase in IP10 (CXCL10) and glutamic acid around the third dose. Post-vaccination IgG response did not alter metabolic profiles like SARS-CoV-2 cases. Our findings provide insights into the safety of repeated COVID-19 vaccinations.

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来源期刊
Journal of Molecular Medicine-Jmm
Journal of Molecular Medicine-Jmm 医学-医学:研究与实验
CiteScore
9.30
自引率
0.00%
发文量
100
审稿时长
1.3 months
期刊介绍: The Journal of Molecular Medicine publishes original research articles and review articles that range from basic findings in mechanisms of disease pathogenesis to therapy. The focus includes all human diseases, including but not limited to: Aging, angiogenesis, autoimmune diseases as well as other inflammatory diseases, cancer, cardiovascular diseases, development and differentiation, endocrinology, gastrointestinal diseases and hepatology, genetics and epigenetics, hematology, hypoxia research, immunology, infectious diseases, metabolic disorders, neuroscience of diseases, -omics based disease research, regenerative medicine, and stem cell research. Studies solely based on cell lines will not be considered. Studies that are based on model organisms will be considered as long as they are directly relevant to human disease.
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