GENE SEQUENCING AS A STRATEGY FOR IDENTIFYING GENETIC FACTORS ASSOCIATED WITH SERIOUS ADVERSE EVENTS AFTER COVID-19 VACCINES IN USE IN BRAZIL

This protocol proposes to investigate genetic factors that may be involved in the pathogenesis of adverse events of interest with selected covid-19 vaccines: vaccine-induced immune thrombotic thrombocytopenia, myocarditis and/or pericarditis and neurological adverse events, such as Guillain-Barré syndrome, acute disseminated encephalomyelitis and transverse myelitis, with the intention of identifying useful biomarkers in identifying people at higher risk, thus reducing the occurrence of these serious adverse events (SAE).

Inclusion Criteria:Sign the ICF by the subject or the subject's legally acceptable representative;Sign the ICF by the participant's family member;Proven vaccination with one of the vaccines for COVID-19 available by the PNI, containing information on the date of application, type (manufacturer) of vaccine received and batch (desirable);Meet the minimum criteria for a level of certainty 3, 2 or 1 in Brighton Collaboration for vaccine-induced immune thrombotic thrombocytopenia as described in 3.2.1.1 OR,Meet the minimum criteria for a level of certainty 3, 2 or 1 in Brighton Collaboration for Myocarditis and/or Pericarditis as described in 3.2.1.2 OR,Meet the minimum criteria for a level of certainty 3, 2 or 1 in Brighton Collaboration for Guillain-Barré syndrome as described in 3.2.1.3 OR,Meet the minimum criteria for a level of certainty 3, 2 or 1 in Brighton Collaboration for Acute Disseminated Encephalomyelitis as described in 3.2.1.4 OR,Meet the minimum criteria for a level of certainty 3, 2 or 1 in Brighton Collaboration for Transverse Myelitis as described in 3.2.1.5 OR,Be classified in the causality categories adopted by the PNI/MS, namely: A1, B1 or B2.Exclusion Criteria:Reports in which it is not possible to retrieve the clinical/laboratory data necessary for evaluation, due to inadequate filling of the notification or unavailability of data;Cases of death in which there are no samples available and/or suitable for carrying out the analyzes defined in the protocol;Cases in which another diagnosis is made for the adverse event of interest, being discarded as a SAE;Cases classified in causality categories (PNI/MS) as A2, A3, A4, C or D;Refusal to sign the informed consent form;