Immunogenicity of BNT162b2 mRNA COVID-19 vaccine and SARS-CoV-2 infection in lung transplant recipients
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články
PubMed
34120839
PubMed Central
PMC8139179
DOI
10.1016/j.healun.2021.05.004
PII: S1053-2498(21)02318-4
Knihovny.cz E-zdroje
- Klíčová slova
- COVID-19, antibody response, immunogenicity, lung transplantation, mRNA vaccine,
- MeSH
- COVID-19 prevence a kontrola MeSH
- imunogenicita vakcíny * MeSH
- lidé středního věku MeSH
- lidé MeSH
- pooperační komplikace prevence a kontrola virologie MeSH
- transplantace plic * MeSH
- tvorba protilátek MeSH
- vakcína BNT162 MeSH
- vakcíny proti COVID-19 imunologie MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- vakcína BNT162 MeSH
- vakcíny proti COVID-19 MeSH
The immunogenicity of the novel mRNA COVID-19 vaccine in immunocompromised lung transplant recipients is still unknown. We compared the antibody response after the first and second doses of the BNT162b2 mRNA COVID-19 vaccine (Pfizer-BioNTech) with the response after natural SARS-CoV-2 infection in lung transplant recipients. None of the vaccinees tested after two doses of the mRNA BNT162b2 vaccine developed anti-SARS-CoV-2 IgG, while 85% patients presented an antibody response after SARS-CoV-2 infection. The absence of antibody response to vaccination led us to investigate the cellular response in a subset of patients. We detected SARS-CoV-2 specific T-cells in 4 out of 12 tested patients. Some patients therefore might have clinical benefit from the vaccine despite an absent antibody response. These results contrast with the excellent antibody response in immunocompetent individuals observed in mRNA BNT162b2 trials and indicate an urgent need to identify the best vaccine type and scheme for immunocompromised transplanted patients.
Zobrazit více v PubMed
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Vaccination Against SARS-CoV-2 in Lung Transplant Recipients: Immunogenicity, Efficacy and Safety
SARS-CoV-2 viral load assessment in lung transplantation