Graves' Disease Following SARS-CoV-2 Vaccination: A Systematic Review

Armando Patrizio1, Silvia Martina Ferrari2, Giusy Elia3

  • 1Department of Emergency Medicine, Azienda Ospedaliero-Universitaria Pisana, 56124 Pisa, Italy.

Vaccines
|September 23, 2022
PubMed

Insights

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccination may trigger Graves' disease (GD) in susceptible individuals. Physicians should monitor for autoimmune endocrine diseases following COVID-19 vaccination.

Area of Science:

  • Endocrinology
  • Immunology
  • Vaccinology

Background:

  • Autoimmune diseases, including autoimmune endocrine diseases (AIED), arise from genetic predisposition and environmental triggers.
  • Vaccines against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are a potential new environmental factor for AIED.
  • Graves' disease (GD) is a specific AIED of concern post-vaccination.

Purpose of the Study:

  • To investigate the association between SARS-CoV-2 vaccination and the onset or recurrence of Graves' disease (GD).
  • To review existing literature on thyroid dysfunction following COVID-19 vaccination.

Main Methods:

  • Literature search of MEDLINE/PubMed databases from January 2020 to July 2022.
  • Inclusion criteria: cases of thyrotoxicosis meeting American Thyroid Association criteria for GD, occurring after SARS-CoV-2 vaccination.
  • Analysis of case reports and case series.

Main Results:

  • 27 articles were identified, detailing 48 new GD diagnoses and 12 GD recurrences post-vaccination.
  • An additional 3 papers reported 3 cases of GD relapse after vaccination.
  • The majority of identified cases involved new-onset or recurrent Graves' disease.

Conclusions:

  • Healthcare providers should be vigilant for Graves' disease and other autoimmune conditions following SARS-CoV-2 vaccination.
  • Individual genetic susceptibility appears crucial for developing post-vaccination autoimmune sequelae.
  • Potential mechanisms include autoimmune/inflammatory syndrome induced by adjuvants (ASIA), cytokine induction, molecular mimicry, and cross-reactivity.

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