Research Centre, Karaganda Medical University, Karaganda, Kazakhstan.
Michael G. DeGroote Institute for Infectious Disease Research, McMaster Immunology Research Centre, Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, ON, Canada.
PLoS One. 2023 Oct 18;18(10):e0293074. doi: 10.1371/journal.pone.0293074. eCollection 2023.
COVID-19 vaccines have played a critical role in controlling the COVID-19 pandemic. Although overall considered safe, COVID-19 vaccination has been associated with rare but severe thrombotic events, occurring mainly in the context of adenoviral vectored vaccines. A better understanding of mechanisms underlying vaccine-induced hypercoagulability and prothrombotic state is needed to improve vaccine safety profile. We assessed changes to the biomarkers of endothelial function (endothelin, ET-1), coagulation (thrombomodulin, THBD and plasminogen activator inhibitor, PAI) and platelet activation (platelet activating factor, PAF, and platelet factor 4 IgG antibody, PF4 IgG) within a three-week period after the first (prime) and second (boost) doses of Gam-Covid-Vac, an AdV5/AdV26-vectored COVID-19 vaccine. Blood plasma collected from vaccinees (n = 58) was assayed using ELISA assays. Participants were stratified by prior COVID-19 exposure based on their baseline SARS-CoV-2-specific serology results. We observed a significant post-prime increase in circulating ET-1, with levels sustained after the boost dose compared to baseline. ET-1 elevation following dose 2 was most pronounced in vaccinees without prior COVID-19 exposure. Prior COVID-19 was also associated with a mild increase in post-dose 1 PAI. Vaccination was associated with elevated ET-1 up to day 21 after the second vaccine dose, while no marked alterations to other biomarkers, including PF4 IgG, were seen. A role of persistent endothelial activation following COVID-19 vaccination warrants further investigation.
COVID-19 疫苗在控制 COVID-19 大流行方面发挥了关键作用。尽管总体上被认为是安全的,但 COVID-19 疫苗接种与罕见但严重的血栓事件有关,这些事件主要发生在腺病毒载体疫苗的背景下。为了提高疫苗的安全性,需要更好地了解疫苗引起的高凝状态和促血栓形成状态的机制。我们评估了 Gam-Covid-Vac(一种 AdV5/AdV26 载体 COVID-19 疫苗)首剂和第 2 剂后 3 周内内皮功能(内皮素,ET-1)、凝血(血栓调节蛋白,THBD 和纤溶酶原激活物抑制剂,PAI)和血小板活化(血小板激活因子,PAF 和血小板因子 4 IgG 抗体,PF4 IgG)生物标志物的变化。使用 ELISA 测定法检测来自疫苗接种者(n=58)的血浆。根据基线 SARS-CoV-2 特异性血清学结果,根据先前 COVID-19 暴露情况对参与者进行分层。我们观察到循环 ET-1 在首剂后显著增加,与基线相比,在加强剂量后仍保持升高。在没有先前 COVID-19 暴露的疫苗接种者中,第 2 剂后 ET-1 升高最为明显。先前 COVID-19 也与第 1 剂后 PAI 轻度增加相关。疫苗接种与第 2 剂后 21 天内 ET-1 升高有关,而其他生物标志物(包括 PF4 IgG)未见明显改变。COVID-19 疫苗接种后持续的内皮激活作用值得进一步研究。