Similarities and differences between myocarditis following COVID-19 mRNA vaccine and multiple inflammatory syndrome

Donato Amodio1, Giuseppe Rubens Pascucci1, Nicola Cotugno1

  • 1Research Unit of Clinical Immunology and Vaccinology, Bambino Gesù Children's Hospital, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Rome, Italy; Department of Systems Medicine, University of Rome "Tor Vergata", Rome, Italy.

PubMed

Insights

Cardiac adverse events following COVID-19 immunization (c-AEFI) and multisystem inflammatory syndrome in children (MIS-C) show distinct inflammatory profiles. c-AEFI patients exhibit higher myocardial injury markers and specific androgen levels, persisting over time.

Area of Science:

  • Cardiology
  • Immunology
  • Pediatrics

Background:

  • Cardiac adverse Events Following COVID-19 Immunization (c-AEFI) and Multisystem Inflammatory Syndrome in Children (MIS-C) with cardiac involvement are observed, particularly in young adult males.
  • Understanding the distinct pathophysiological mechanisms of these post-immunization and post-infectious cardiac conditions is crucial.

Purpose of the Study:

  • To compare the inflammatory profiles and specific biomarkers in patients with c-AEFI versus MIS-C with cardiac involvement.
  • To investigate the presence of autoantibodies targeting cardiac and endothelial cells in these conditions.

Main Methods:

  • Comparative analysis of inflammatory protein profiles between c-AEFI and MIS-C patient cohorts.
  • Measurement of serum DHEAS, DHEA, and cortisone levels.
  • Screening for anti-heart muscle and anti-endothelial cell antibodies.

Main Results:

  • MIS-C patients showed higher levels of systemic inflammation proteins compared to c-AEFI patients.
  • c-AEFI patients exhibited elevated levels of proteins associated with myocardial injury.
  • Higher levels of DHEAS, DHEA, and cortisone were detected in c-AEFI patients, persisting at follow-up.
  • No anti-heart muscle or anti-endothelial cell antibodies were found in either group.

Conclusions:

  • c-AEFI and MIS-C with cardiac involvement present with distinct inflammatory and androgen profiles.
  • c-AEFI appears to be a localized cardiac condition with a unique hormonal signature.
  • These findings suggest different underlying mechanisms for cardiac complications following COVID-19 immunization versus MIS-C.

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