Department of Biomedical Science, Jungwon University, Goesan-gun, Chungbuk, Republic of Korea.
Department of Medical and Biological Sciences, The Catholic University of Korea, Gyeonggi-do, Bucheon, Republic of Korea.
PLoS One. 2024 Oct 10;19(10):e0311726. doi: 10.1371/journal.pone.0311726. eCollection 2024.
The current COVID-19 mRNA vaccines were developed and applied for pandemic-emergent conditions. These vaccines use a small piece of the virus's genetic material (mRNA) to stimulate an immune response against COVID-19. However, their potential effects on individuals with chronic inflammatory conditions and vaccination routes remain questionable. Therefore, we investigated the effects of mRNA vaccines in a mouse model of chronic inflammation, focusing on their cardiac toxicity and immunogenicity dependent on the injection route. mRNA vaccine intravenous administration with or without chronic inflammation exacerbated cardiac pericarditis and myocarditis; immunization induced mild inflammation and inflammatory cytokine IL-1beta and IL-6 production in the heart. Further, IV mRNA vaccination induced cardiac damage in LPS chronic inflammation, particularly serum troponin I (TnI), which dramatically increased. IV vaccine administration may induce more cardiotoxicity in chronic inflammation. These findings highlight the need for further research to understand the underlying mechanisms of mRNA vaccines with chronic inflammatory conditions dependent on injection routes.
当前的 COVID-19 mRNA 疫苗是为应对大流行紧急情况而开发和应用的。这些疫苗使用一小段病毒的遗传物质(mRNA)来刺激针对 COVID-19 的免疫反应。然而,它们对患有慢性炎症性疾病的个体和接种途径的潜在影响仍存在疑问。因此,我们在慢性炎症的小鼠模型中研究了 mRNA 疫苗的作用,重点研究了其心脏毒性和免疫原性与注射途径的关系。mRNA 疫苗静脉注射加或不加慢性炎症会加重心脏心包炎和心肌炎;免疫接种会引起心脏轻度炎症和炎性细胞因子 IL-1beta 和 IL-6 的产生。此外,LPS 慢性炎症中的 IV mRNA 疫苗接种会导致心脏损伤,尤其是血清肌钙蛋白 I(TnI)显著增加。IV 疫苗给药可能会在慢性炎症中引起更多的心脏毒性。这些发现强调需要进一步研究,以了解依赖于注射途径的慢性炎症条件下 mRNA 疫苗的潜在机制。