Abstract
SARS CoV-2 enters host cells via its Spike protein moiety binding to the essential cardiac enzyme angiotensin-converting enzyme (ACE) 2, followed by internalization. COVID-19 mRNA vaccines are RNA sequences that are translated into Spike protein, which follows the same ACE2-binding route as the intact virion. In model systems, isolated Spike protein can produce cell damage and altered gene expression, and myocardial injuryor myocarditis can occur during COVID-19 or after mRNA vaccination. We investigated 7 COVID-19 and6 post-mRNA vaccination patients with myocardial injury and found nearly identical alterations in geneexpression that would predispose to inflammation, coagulopathy, and myocardial dysfunction.
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