Background: Myocarditis, even in a severe and lethal form, may occur after COVID-19 mRNA (BNT162b2) vaccination. However, its pathway, morphomolecular characterization and treatment are still unknown. Methods: Routine hematochemical screening, ECG, Holter monitoring, 2D echocardiogram cardiac magnetic resonance (CMR) and invasive cardiac studies (cardiac catheterization, selective coronary angiography, left ventriculography and left ventricular endomyocardial biopsy) are reported from three patients (39F-pt1, 78M-pt2, 52M-pt3) with severe compromise of conduction tissue (junctional rhythm and syncope, pt1) or cardiac function compromise (LVEF <= 35%, pt2 and pt3) after COVID-19 mRNA (BNT162b2). Results: Hematochemical data and coronary angiography were normal in the patients studied. Histology showed in all three patients extensive myocardial infiltration of degranulated eosinophils and elevation of serum cationic protein directly responsible for cardiomyocyte damage. These findings demonstrate myocarditis hypersensitivity to some component of the vaccine (spike protein?) acting as a hapten to some macromolecules of cardiomyocytes. Steroid administration (prednisone, 1 mg/kg die for 3 days, followed by 0.33 mg/kg for 4 weeks) was followed by complete recovery of cardiac contractility in pt2 and pt3. Conclusions: Eosinophilic myocarditis is a possible adverse reaction to the mRNA COVID-19 vaccine. Its pathway is mediated by release of cationic protein and responds to short courses of steroid administration.

Hypersensitivity myocarditis after COVID-19 mRNA vaccination / Frustaci, Andrea; Verardo, Romina; Galea, Nicola; Lavalle, Carlo; Bagnato, Giulia; Scialla, Rossella; Chimenti, Cristina. - In: JOURNAL OF CLINICAL MEDICINE. - ISSN 2077-0383. - 11:6(2022). [10.3390/jcm11061660]

Hypersensitivity myocarditis after COVID-19 mRNA vaccination

Frustaci, Andrea
Primo
Conceptualization
;
Verardo, Romina
Secondo
Writing – Review & Editing
;
Galea, Nicola
Writing – Original Draft Preparation
;
Lavalle, Carlo
Software
;
Bagnato, Giulia
Formal Analysis
;
Chimenti, Cristina
Ultimo
2022

Abstract

Background: Myocarditis, even in a severe and lethal form, may occur after COVID-19 mRNA (BNT162b2) vaccination. However, its pathway, morphomolecular characterization and treatment are still unknown. Methods: Routine hematochemical screening, ECG, Holter monitoring, 2D echocardiogram cardiac magnetic resonance (CMR) and invasive cardiac studies (cardiac catheterization, selective coronary angiography, left ventriculography and left ventricular endomyocardial biopsy) are reported from three patients (39F-pt1, 78M-pt2, 52M-pt3) with severe compromise of conduction tissue (junctional rhythm and syncope, pt1) or cardiac function compromise (LVEF <= 35%, pt2 and pt3) after COVID-19 mRNA (BNT162b2). Results: Hematochemical data and coronary angiography were normal in the patients studied. Histology showed in all three patients extensive myocardial infiltration of degranulated eosinophils and elevation of serum cationic protein directly responsible for cardiomyocyte damage. These findings demonstrate myocarditis hypersensitivity to some component of the vaccine (spike protein?) acting as a hapten to some macromolecules of cardiomyocytes. Steroid administration (prednisone, 1 mg/kg die for 3 days, followed by 0.33 mg/kg for 4 weeks) was followed by complete recovery of cardiac contractility in pt2 and pt3. Conclusions: Eosinophilic myocarditis is a possible adverse reaction to the mRNA COVID-19 vaccine. Its pathway is mediated by release of cationic protein and responds to short courses of steroid administration.
2022
COVID-19 mRNA vaccination; eosinophilic myocarditis; myocarditis
01 Pubblicazione su rivista::01a Articolo in rivista
Hypersensitivity myocarditis after COVID-19 mRNA vaccination / Frustaci, Andrea; Verardo, Romina; Galea, Nicola; Lavalle, Carlo; Bagnato, Giulia; Scialla, Rossella; Chimenti, Cristina. - In: JOURNAL OF CLINICAL MEDICINE. - ISSN 2077-0383. - 11:6(2022). [10.3390/jcm11061660]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1682029
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