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Antibody Response to COVID-19 Booster Vaccination in Healthcare Workers.
Pani, Arianna; Romandini, Alessandra; Schianchi, Alice; Senatore, Michele; Gagliardi, Oscar M; Gazzaniga, Gianluca; Agliardi, Stefano; Conti, Tommaso; Schenardi, Paolo A; Maggi, Matteo; D'Onghia, Stefano; Panetta, Valentina; Renica, Silvia; Molteni, Silvia Nerini; Vismara, Chiara; Campisi, Daniela; Bertuzzi, Michaela; Giroldi, Simona; Zoppini, Laura; Moreno, Mauro; Merli, Marco; Bosio, Marco; Puoti, Massimo; Scaglione, Francesco.
  • Pani A; Oncology and Hemato-Oncology Department, Università degli Studi di Milano, Milan, Italy.
  • Romandini A; Oncology and Hemato-Oncology Department, Università degli Studi di Milano, Milan, Italy.
  • Schianchi A; Oncology and Hemato-Oncology Department, Università degli Studi di Milano, Milan, Italy.
  • Senatore M; Oncology and Hemato-Oncology Department, Università degli Studi di Milano, Milan, Italy.
  • Gagliardi OM; Chemical-Clinical Analysis Unit, Laboratory Medicine Department, Niguarda Hospital, Milan, Italy.
  • Gazzaniga G; Oncology and Hemato-Oncology Department, Università degli Studi di Milano, Milan, Italy.
  • Agliardi S; Oncology and Hemato-Oncology Department, Università degli Studi di Milano, Milan, Italy.
  • Conti T; Oncology and Hemato-Oncology Department, Università degli Studi di Milano, Milan, Italy.
  • Schenardi PA; Oncology and Hemato-Oncology Department, Università degli Studi di Milano, Milan, Italy.
  • Maggi M; Oncology and Hemato-Oncology Department, Università degli Studi di Milano, Milan, Italy.
  • D'Onghia S; Oncology and Hemato-Oncology Department, Università degli Studi di Milano, Milan, Italy.
  • Panetta V; Oncology and Hemato-Oncology Department, Università degli Studi di Milano, Milan, Italy.
  • Renica S; Biostatistics Office, L'altrastatistica srl - Consultancy & Training, Rome, Italy.
  • Molteni SN; Microbiology Unit, Laboratory Medicine Department, Niguarda Hospital, Milan, Italy.
  • Vismara C; Microbiology Unit, Laboratory Medicine Department, Niguarda Hospital, Milan, Italy.
  • Campisi D; Microbiology Unit, Laboratory Medicine Department, Niguarda Hospital, Milan, Italy.
  • Bertuzzi M; Microbiology Unit, Laboratory Medicine Department, Niguarda Hospital, Milan, Italy.
  • Giroldi S; Quality & Risk Control in Data Management, Azienda Socio Sanitaria Territoriale (ASST) Grande Ospedale Metropolitano Niguarda, Milan, Italy.
  • Zoppini L; Socio-sanitary Direction, Azienda Socio Sanitaria Territoriale (ASST) Grande Ospedale Metropolitano Niguarda, Milan, Italy.
  • Moreno M; Socio-sanitary Direction, Azienda Socio Sanitaria Territoriale (ASST) Grande Ospedale Metropolitano Niguarda, Milan, Italy.
  • Merli M; Healthcare Management Department, Azienda Socio Sanitaria Territoriale (ASST) Grande Ospedale Metropolitano Niguarda, Milan, Italy.
  • Bosio M; Infectious Diseases Unit, Azienda Socio Sanitaria Territoriale (ASST) Grande Ospedale Metropolitano Niguarda, Milan, Italy.
  • Puoti M; Healthcare Management Department, Azienda Socio Sanitaria Territoriale (ASST) Grande Ospedale Metropolitano Niguarda, Milan, Italy.
  • Scaglione F; Infectious Diseases Unit, Azienda Socio Sanitaria Territoriale (ASST) Grande Ospedale Metropolitano Niguarda, Milan, Italy.
Front Immunol ; 13: 872667, 2022.
Article in English | MEDLINE | ID: covidwho-1903012
ABSTRACT

Objective:

To evaluate the mean increase of anti-S IgG antibody titer between the basal, pre-booster level to the titer assessed 14 days after the booster dose of BNT162b2. Patients and

Methods:

The RENAISSANCE study is an observational, longitudinal, prospective, population-based study, conducted on healthcare workers of Niguarda Hospital in Milan, Italy who received a BNT162b2 booster dose at least 180 days after their second dose or after positivity for SARS-CoV-2 and accepted to take part in the study. The RENAISSANCE study was conducted from January 1, 2021 through December 28, 2021.

Findings:

1,738 subjects were enrolled among healthcare workers registered for the booster administration at our hospital. Overall, 0.4% of subjects were seronegative at the pre-booster evaluation, and 1 subject had a titer equal to 50 AU/ml none of the evaluated subjects was seronegative after the booster dose. Thus, the efficacy of the booster in our population was universal. Mean increase of pre- to post-booster titer was more significant in subjects who never had SARS-CoV-2 (44 times CI 95% 42-46) compared to those who had it, before (33 times, CI 95% 13-70) or after the first vaccination cycle (12 times, CI 95% 11-14). Differently from sex, age and pre-booster titers affected the post-booster antibody response. Nevertheless, the post-booster titer was very similar in all subgroups, and independent of a prior exposure to SARS-CoV-2, pre-booster titer, sex or age.

Conclusion:

Our study shows a potent universal antibody response of the booster dose of BNT162b2, regardless of pre-booster vaccine seronegativity.
Subject(s)
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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 / Antibody Formation Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study Topics: Vaccines Limits: Humans Language: English Journal: Front Immunol Year: 2022 Document Type: Article Affiliation country: Fimmu.2022.872667

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 / Antibody Formation Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study Topics: Vaccines Limits: Humans Language: English Journal: Front Immunol Year: 2022 Document Type: Article Affiliation country: Fimmu.2022.872667