SARS-CoV2 mRNA vaccine intravenous administration induces myocarditis in chronic inflammation

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.

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Publication Details

Journal
PLoS ONE
Published
2024-10-10
DOI
https://doi.org/10.1371/journal.pone.0311726
Citations
7
Primary Topic
Viral Infections and Immunology Research
Type
article
Field-Weighted Citation Impact
2.81

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SARS-CoV2 mRNA vaccine intravenous administration induces myocarditis in chronic inflammation

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SARS-CoV2 mRNA vaccine intravenous administration induces myocarditis in chronic inflammation

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article en
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Abstract

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.

PLoS ONEVol. 19(10)
Samsung Medical Center (KR), Jungwon University (KR), Catholic University of Korea (KR)
Ministry of Food and Drug Safety, Korea Health Industry Development Institute, National Institute of Food and Drug Safety Evaluation
Good health and well-being
Openalex Percentile: Top 8%
Viral Infections and Immunology Research
2.81
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