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Immunogenicity and Safety of Anti-SARS-CoV-2 mRNA Vaccines in a Cohort of Patients with Hereditary Angioedema.
Mormile, Ilaria; Gigliotti, Maria Celeste; Petraroli, Angelica; Cocchiaro, Antonio; Furno, Alessandro; Granata, Francescopaolo; Rossi, Francesca Wanda; Portella, Giuseppe; de Paulis, Amato.
Affiliation
  • Mormile I; Department of Translational Medical Sciences, University of Naples Federico II, 80131 Naples, Italy.
  • Gigliotti MC; Department of Translational Medical Sciences, University of Naples Federico II, 80131 Naples, Italy.
  • Petraroli A; Department of Translational Medical Sciences, University of Naples Federico II, 80131 Naples, Italy.
  • Cocchiaro A; Department of Translational Medical Sciences, University of Naples Federico II, 80131 Naples, Italy.
  • Furno A; Department of Translational Medical Sciences, University of Naples Federico II, 80131 Naples, Italy.
  • Granata F; Department of Translational Medical Sciences, University of Naples Federico II, 80131 Naples, Italy.
  • Rossi FW; Department of Translational Medical Sciences, University of Naples Federico II, 80131 Naples, Italy.
  • Portella G; Center for Basic and Clinical Immunology Research (CISI), University of Naples Federico II, 80131 Naples, Italy.
  • de Paulis A; WAO Center of Excellence, 80131 Naples, Italy.
Vaccines (Basel) ; 11(2)2023 Jan 18.
Article de En | MEDLINE | ID: mdl-36851094
ABSTRACT
Many factors may trigger hereditary angioedema (HAE) attacks. This study aims to gain insights into the benefits and potential risks of COVID-19 vaccination in HAE patients, focusing particularly on the possibility of triggering attacks. We enrolled 31 patients with HAE undergoing two doses of the SARS-CoV-2 mRNA Comirnaty-BioNTech/Pfizer vaccine. To evaluate the possible influence of the vaccine on disease control and attack frequency, we administered the angioedema control test (AECT) 4-week version before (T0), 21 days after the first dose (T1), and between 21 and 28 days after the second dose (T2). Despite 5 patients (16.1%) experiencing attacks within 72 h of the first dose administration, no significant variation in attack frequency was observed before and after vaccination [F(2,60) = 0.123; p = 0.799]. In addition, patients reported higher AECT scores at T1 and T2 compared to T0 [F(2,44) = 6.541; p < 0.05; post hoc p < 0.05)], indicating that the disease was rather more controlled after vaccinations than in the previous period. All patients showed a positive serological response to the vaccine without significant differences from healthy controls (U = 162; p = 0.062). These observations suggest that the vaccine administration is safe and effective in HAE patients.
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Type d'étude: Risk_factors_studies Langue: En Journal: Vaccines (Basel) Année: 2023 Type de document: Article Pays d'affiliation: Italie

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Type d'étude: Risk_factors_studies Langue: En Journal: Vaccines (Basel) Année: 2023 Type de document: Article Pays d'affiliation: Italie