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Healthcare Worker Study Cohort to Determine the Level and Durability of Cellular and Humoral Immune Responses after Two Doses of SARS-CoV-2 Vaccination.
Dentone, Chiara; Fenoglio, Daniela; Ponzano, Marta; Cerchiaro, Matteo; Altosole, Tiziana; Franciotta, Diego; Portunato, Federica; Mikulska, Malgorzata; Taramasso, Lucia; Magnasco, Laura; Uras, Chiara; Magne, Federica; Ferrera, Francesca; Scavone, Graziana; Signori, Alessio; Vena, Antonio; Visconti, Valeria; Filaci, Gilberto; Sette, Alessandro; Grifoni, Alba; Di Biagio, Antonio; Bassetti, Matteo.
  • Dentone C; Infectious Disease Clinic, IRCCS Policlinico San Martino Hospital, Largo Rosanna Benzi, 10, 16132 Genoa, Italy.
  • Fenoglio D; Department of Internal Medicine, Centre of Excellence for Biomedical Research (CEBR), University of Genoa, 16126 Genoa, Italy.
  • Ponzano M; Biotherapy Unit, IRCCS Policlinico San Martino, 16132 Genoa, Italy.
  • Cerchiaro M; Biostatistics Unit, Department of Health Science, University of Genova, 16132 Genova, Italy.
  • Altosole T; Infectious Diseases Unit, Department of Health Science (DISSAL), University of Genoa, 16126 Genoa, Italy.
  • Franciotta D; Department of Internal Medicine, Centre of Excellence for Biomedical Research (CEBR), University of Genoa, 16126 Genoa, Italy.
  • Portunato F; Autoimmunology Laboratory, IRCCS Policlinico San Martino, 16132 Genoa, Italy.
  • Mikulska M; Infectious Disease Clinic, IRCCS Policlinico San Martino Hospital, Largo Rosanna Benzi, 10, 16132 Genoa, Italy.
  • Taramasso L; Infectious Disease Clinic, IRCCS Policlinico San Martino Hospital, Largo Rosanna Benzi, 10, 16132 Genoa, Italy.
  • Magnasco L; Infectious Diseases Unit, Department of Health Science (DISSAL), University of Genoa, 16126 Genoa, Italy.
  • Uras C; Infectious Disease Clinic, IRCCS Policlinico San Martino Hospital, Largo Rosanna Benzi, 10, 16132 Genoa, Italy.
  • Magne F; Infectious Disease Clinic, IRCCS Policlinico San Martino Hospital, Largo Rosanna Benzi, 10, 16132 Genoa, Italy.
  • Ferrera F; Department of Internal Medicine, Centre of Excellence for Biomedical Research (CEBR), University of Genoa, 16126 Genoa, Italy.
  • Scavone G; Infectious Disease Clinic, IRCCS Policlinico San Martino Hospital, Largo Rosanna Benzi, 10, 16132 Genoa, Italy.
  • Signori A; Department of Internal Medicine, Centre of Excellence for Biomedical Research (CEBR), University of Genoa, 16126 Genoa, Italy.
  • Vena A; Biotherapy Unit, IRCCS Policlinico San Martino, 16132 Genoa, Italy.
  • Visconti V; Biostatistics Unit, Department of Health Science, University of Genova, 16132 Genova, Italy.
  • Filaci G; Infectious Disease Clinic, IRCCS Policlinico San Martino Hospital, Largo Rosanna Benzi, 10, 16132 Genoa, Italy.
  • Sette A; Laboratory Unit, IRCCS Policlinico San Martino, 16132 Genoa, Italy.
  • Grifoni A; Department of Internal Medicine, Centre of Excellence for Biomedical Research (CEBR), University of Genoa, 16126 Genoa, Italy.
  • Di Biagio A; Biotherapy Unit, IRCCS Policlinico San Martino, 16132 Genoa, Italy.
  • Bassetti M; Center for Infectious Disease and Vaccine Research, La Jolla Institute for Immunology (LJI), La Jolla, CA 92037, USA.
Vaccines (Basel) ; 10(11)2022 Oct 24.
Article in English | MEDLINE | ID: covidwho-2081926
ABSTRACT
We prospectively studied immunological response against SARS-CoV-2 after vaccination among healthcare workers without (group A) and with previous infection (group B). The analyses were collected at T0 (before the BNT162b2), T1 (before the second dose), T2 and T6 (1 and 6 months after the second dose). For cellular immune response, the activation-induced cell marker assay was performed with CD4 and CD8 Spike peptide megapools expressed as Stimulation Index. For humoral immune response, we determined antibodies to Spike-1 and nucleocapsid protein. The linear mixed model compared specific times to T0. The CD4+ Spike response overall rate of change was significant at T1 (p = 0.038) and at T2 (p < 0.001), while decreasing at T6. For CD8+ Spike reactivity, the interaction between the time and group was significant (p = 0.0265), and the p value for group comparison was significant at the baseline (p = 0.0030) with higher SI in previously infected subjects. Overall, the anti-S Abs significantly increased from T1 to T6 compared to T0. The group B at T6 retained high anti-S titer (p < 0.001). At T6, in both groups we found a persistent humoral response and a high CD4+ T cell response able to cross recognize SARS-COV-2 variants including epsilon, even if not a circulating virus at that time.
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Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Topics: Vaccines / Variants Language: English Year: 2022 Document Type: Article Affiliation country: Vaccines10111784

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Topics: Vaccines / Variants Language: English Year: 2022 Document Type: Article Affiliation country: Vaccines10111784