Increased Mild Vaccine-Related Side Effects and Higher Specific Antibody Titers in Health Care Workers with Previous SARS-CoV-2 Infection after the mRNA BNT162b2 Vaccine.

BNT162b2 COVID-19 SARS-CoV-2 antibody titer healthcare workers side effects vaccines

Journal

Vaccines
ISSN: 2076-393X
Titre abrégé: Vaccines (Basel)
Pays: Switzerland
ID NLM: 101629355

Informations de publication

Date de publication:
02 Aug 2022
Historique:
received: 27 05 2022
revised: 28 07 2022
accepted: 29 07 2022
entrez: 26 8 2022
pubmed: 27 8 2022
medline: 27 8 2022
Statut: epublish

Résumé

Background: to evaluate whether prior SARS-CoV-2 infection affects side effects and specific antibody production after vaccination with BNT162b2. Methods: We included 1106 health care workers vaccinated with BNT162b2. We assessed whether prior SARS-CoV-2 infection affects the number and type of side effects and performed a nested case−control analysis comparing plasma levels of specific IgG titers between SARS-CoV-2-naïve and previously infected subjects after the first and the second vaccine doses. Results: After the first dose, SARS-CoV-2-naïve subjects experienced side effects more often than SARS-CoV-2 naïve subjects. Individuals with prior SARS-CoV-2 infection more often reported pain at the injection site, weakness, and fever than SARS-CoV-2-naïve subjects. After the second dose, the frequency of side effects was similar in the two groups. All subjects with prior SARS-CoV-2 infection developed either a high (>100 AU/mL) or intermediate (10−100 AU/mL) antibody titer. Among SARS-CoV-2-naïve subjects, the majority developed an intermediate titer. After the second dose, a high (>2000 AU/mL) antibody titer was more common among subjects with prior SARS-CoV-2 infection. Conclusions: vaccine-related side effects and a higher anti-SARS-CoV-2-RBD IgG titer were more common in subjects with previous infection than in SARS-CoV-2-naïve after the first, but not after the second dose of the BNT162b2 vaccine.

Identifiants

pubmed: 36016128
pii: vaccines10081238
doi: 10.3390/vaccines10081238
pmc: PMC9414957
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Ludovica Ferrari (L)

Infectious Diseases Clinic, Policlinic of Tor Vergata, 00133 Rome, Italy.

Mirko Compagno (M)

Infectious Diseases Clinic, Policlinic of Tor Vergata, 00133 Rome, Italy.

Laura Campogiani (L)

Infectious Diseases Clinic, Policlinic of Tor Vergata, 00133 Rome, Italy.

Elisabetta Teti (E)

Infectious Diseases Clinic, Policlinic of Tor Vergata, 00133 Rome, Italy.

Tiziana Mulas (T)

Infectious Diseases Clinic, Policlinic of Tor Vergata, 00133 Rome, Italy.

Davide Checchi (D)

Infectious Diseases Clinic, Policlinic of Tor Vergata, 00133 Rome, Italy.

Grazia Alessio (G)

Infectious Diseases Clinic, Policlinic of Tor Vergata, 00133 Rome, Italy.

Federica Caldara (F)

Infectious Diseases Clinic, Policlinic of Tor Vergata, 00133 Rome, Italy.

Luigi Coppola (L)

Infectious Diseases Clinic, Policlinic of Tor Vergata, 00133 Rome, Italy.

Giuseppe De Simone (G)

Infectious Diseases Clinic, Policlinic of Tor Vergata, 00133 Rome, Italy.

Laura Ceccarelli (L)

Infectious Diseases Clinic, Policlinic of Tor Vergata, 00133 Rome, Italy.

Ilaria Spalliera (I)

Infectious Diseases Clinic, Policlinic of Tor Vergata, 00133 Rome, Italy.

Pietro Vitale (P)

Infectious Diseases Clinic, Policlinic of Tor Vergata, 00133 Rome, Italy.

Sandro Grelli (S)

Department of Experimental Medicine, University of Rome Tor Vergata, 00133 Rome, Italy.
Virology Unit, Policlinic of Tor Vergata, 00133 Rome, Italy.

Massimo Andreoni (M)

Department of Systems Medicine, University of Rome Tor Vergata, Via Montpellier 1, 00133 Rome, Italy.

Loredana Sarmati (L)

Department of Systems Medicine, University of Rome Tor Vergata, Via Montpellier 1, 00133 Rome, Italy.

Marco Iannetta (M)

Department of Systems Medicine, University of Rome Tor Vergata, Via Montpellier 1, 00133 Rome, Italy.

Classifications MeSH