Safety and cross-variant immunogenicity of a three-dose COVID-19 mRNA vaccine regimen in kidney transplant recipients

The immunogenicity of a two-dose mRNA COVID-19 vaccine regimen is low in kidney transplant (KT) recipients. Here, we provide a thorough assessment of the immunogenicity of a three-dose COVID-19 vaccine regimen in this population. We performed a prospective longitudinal study in sixty-one KT recipien...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:EBioMedicine 2021-11, Vol.73, p.103679-103679, Article 103679
Hauptverfasser: Massa, Filippo, Cremoni, Marion, Gérard, Alexandre, Grabsi, Hanen, Rogier, Lory, Blois, Mathilde, Couzin, Chloé, Hassen, Nadia Ben, Rouleau, Matthieu, Barbosa, Susana, Martinuzzi, Emanuela, Fayada, Julien, Bernard, Ghislaine, Favre, Guillaume, Hofman, Paul, Esnault, Vincent L.M., Czerkinsky, Cecil, Seitz-Polski, Barbara, Glaichenhaus, Nicolas, Sicard, Antoine
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:The immunogenicity of a two-dose mRNA COVID-19 vaccine regimen is low in kidney transplant (KT) recipients. Here, we provide a thorough assessment of the immunogenicity of a three-dose COVID-19 vaccine regimen in this population. We performed a prospective longitudinal study in sixty-one KT recipients given three doses of the BNT162b2 COVID-19 vaccine. We performed semi-structured pharmacovigilance interviews and monitored donor-specific antibodies and kidney function. We compared levels of anti-spike IgG, pseudo-neutralization activity against vaccine homologous and heterologous variants, frequency of spike-specific interferon (IFN)-γ-secreting cells, and antigen-induced cytokine production 28 days after the second and third doses. Reactions to vaccine were mild. One patient developed donor-specific anti-HLA antibodies after the second dose which could be explained by non-adherence to immunosuppressive therapy. Spike-specific IgG seroconversion raised from 44·3% (n=27) after the second dose to 62·3% (n=38) after the third dose (p
ISSN:2352-3964
2352-3964
DOI:10.1016/j.ebiom.2021.103679