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Kinetics and persistence of cellular and humoral immune responses to SARS-CoV-2 vaccine in healthcare workers with or without prior COVID-19.
Chivu-Economescu, Mihaela; Bleotu, Coralia; Grancea, Camelia; Chiriac, Daniela; Botezatu, Anca; Iancu, Iulia V; Pitica, Ioana; Necula, Laura G; Neagu, Ana; Matei, Lilia; Dragu, Denisa; Sultana, Camelia; Radu, Elena L; Nastasie, Alina; Voicu, Oana; Ataman, Marius; Nedeianu, Saviana; Mambet, Cristina; Diaconu, Carmen C; Ruta, Simona Maria.
  • Chivu-Economescu M; Stefan S. Nicolau Institute of Virology, Bucharest, Romania.
  • Bleotu C; Stefan S. Nicolau Institute of Virology, Bucharest, Romania.
  • Grancea C; Stefan S. Nicolau Institute of Virology, Bucharest, Romania.
  • Chiriac D; Stefan S. Nicolau Institute of Virology, Bucharest, Romania.
  • Botezatu A; Stefan S. Nicolau Institute of Virology, Bucharest, Romania.
  • Iancu IV; Stefan S. Nicolau Institute of Virology, Bucharest, Romania.
  • Pitica I; Stefan S. Nicolau Institute of Virology, Bucharest, Romania.
  • Necula LG; Stefan S. Nicolau Institute of Virology, Bucharest, Romania.
  • Neagu A; Stefan S. Nicolau Institute of Virology, Bucharest, Romania.
  • Matei L; Stefan S. Nicolau Institute of Virology, Bucharest, Romania.
  • Dragu D; Stefan S. Nicolau Institute of Virology, Bucharest, Romania.
  • Sultana C; Stefan S. Nicolau Institute of Virology, Bucharest, Romania.
  • Radu EL; Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.
  • Nastasie A; Stefan S. Nicolau Institute of Virology, Bucharest, Romania.
  • Voicu O; Institute for Water Quality and Resource Management TU Wien, Vienna, Austria.
  • Ataman M; Stefan S. Nicolau Institute of Virology, Bucharest, Romania.
  • Nedeianu S; Stefan S. Nicolau Institute of Virology, Bucharest, Romania.
  • Mambet C; Stefan S. Nicolau Institute of Virology, Bucharest, Romania.
  • Diaconu CC; Stefan S. Nicolau Institute of Virology, Bucharest, Romania.
  • Ruta SM; Stefan S. Nicolau Institute of Virology, Bucharest, Romania.
J Cell Mol Med ; 26(4): 1293-1305, 2022 02.
Article in English | MEDLINE | ID: covidwho-1626165
ABSTRACT
SARS-CoV-2 vaccines are highly efficient against severe forms of the disease, hospitalization and death. Nevertheless, insufficient protection against several circulating viral variants might suggest waning immunity and the need for an additional vaccine dose. We conducted a longitudinal study on the kinetics and persistence of immune responses in healthcare workers vaccinated with two doses of BNT162b2 mRNA vaccine with or without prior SARS-CoV-2 infection. No new infections were diagnosed during follow-up. At 6 months, post-vaccination or post-infection, despite a downward trend in the level of anti-S IgG antibodies, the neutralizing activity does not decrease significantly, remaining higher than 75% (85.14% for subjects with natural infection, 88.82% for vaccinated after prior infection and 78.37% for vaccinated only). In a live-virus neutralization assay, the highest neutralization titres were present at baseline and at 6 months follow-up in persons vaccinated after prior infection. Anti-S IgA levels showed a significant descending trend in vaccinated subjects (p < 0.05) after 14 weeks. Cellular immune responses are present even in vaccinated participants with declining antibody levels (index ratio 1.1-3) or low neutralizing activity (30%-40%) at 6 months, although with lower T-cell stimulation index (p = 0.046) and IFN-γ secretion (p = 0.0007) compared to those with preserved humoral responses.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Immunity, Humoral / COVID-19 / BNT162 Vaccine / Immunity, Cellular Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines / Variants Limits: Adult / Humans / Middle aged Language: English Journal: J Cell Mol Med Journal subject: Molecular Biology Year: 2022 Document Type: Article Affiliation country: Jcmm.17186

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Immunity, Humoral / COVID-19 / BNT162 Vaccine / Immunity, Cellular Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines / Variants Limits: Adult / Humans / Middle aged Language: English Journal: J Cell Mol Med Journal subject: Molecular Biology Year: 2022 Document Type: Article Affiliation country: Jcmm.17186