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https://doi.org/10.1016/j.medj.2023.04.001
Title: | RNase2 is a possible trigger of acute-on-chronic inflammation leading to mRNA vaccine-associated cardiac complication. | Authors: | Ong, Eugenia Z Koh, Clara WT Tng, Danny JH Ooi, Justin SG Yee, Jia Xin Chew, Valerie SY Leong, Yan Shan Gunasegaran, Kurugulasigamoney Yeo, Chin Pin Oon, Lynette LE Sim, Jean XY Chan, Kuan Rong Low, Jenny G Ooi, Eng Eong |
Keywords: | COVID-19 RNASE2 Translation to patients cardiac complication mRNA vaccination severe adverse event |
Issue Date: | 21-Apr-2023 | Publisher: | Elsevier BV | Citation: | Ong, Eugenia Z, Koh, Clara WT, Tng, Danny JH, Ooi, Justin SG, Yee, Jia Xin, Chew, Valerie SY, Leong, Yan Shan, Gunasegaran, Kurugulasigamoney, Yeo, Chin Pin, Oon, Lynette LE, Sim, Jean XY, Chan, Kuan Rong, Low, Jenny G, Ooi, Eng Eong (2023-04-21). RNase2 is a possible trigger of acute-on-chronic inflammation leading to mRNA vaccine-associated cardiac complication.. Med : S2666-6340(23)00104-6-. ScholarBank@NUS Repository. https://doi.org/10.1016/j.medj.2023.04.001 | Abstract: | BACKGROUND: Post-mRNA vaccination-associated cardiac complication is a rare but life-threatening adverse event. Its risk has been well balanced by the benefit of vaccination-induced protection against severe COVID-19. As the rate of severe COVID-19 has consequently declined, future booster vaccination to sustain immunity, especially against infection with new severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants, may encounter benefit-risk ratios that are less favorable than at the start of the COVID-19 vaccination campaign. Understanding the pathogenesis of rare but severe vaccine-associated adverse events to minimize its risk is thus urgent. METHODS: Here, we report a serendipitous finding of a case of cardiac complication following a third shot of COVID-19 mRNA vaccine. As this case was enrolled in a cohort study, pre-vaccination and pre-symptomatic blood samples were available for genomic and multiplex cytokine analyses. FINDINGS: These analyses revealed the presence of subclinical chronic inflammation, with an elevated expression of RNASE2 at pre-booster baseline as a possible trigger of an acute-on-chronic inflammation that resulted in the cardiac complication. RNASE2 encodes for the ribonuclease RNase2, which cleaves RNA at the 3' side of uridine, which may thus remove the only Toll-like receptor (TLR)-avoidance safety feature of current mRNA vaccines. CONCLUSIONS: These pre-booster and pre-symptomatic gene and cytokine expression data provide unique insights into the possible pathogenesis of vaccine-associated cardiac complication and suggest the incorporation of additional nucleoside modification for an added safety margin. FUNDING: This work was funded by the NMRC Open Fund-Large Collaborative Grant on Integrated Innovations on Infectious Diseases (OFLCG19May-0034). | Source Title: | Med | URI: | https://scholarbank.nus.edu.sg/handle/10635/241683 | ISSN: | 2666-6359 2666-6340 |
DOI: | 10.1016/j.medj.2023.04.001 |
Appears in Collections: | Staff Publications Elements |
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