Virological and Serological Characterisation of SARS-CoV-2 Infections Diagnosed After mRNA BNT162b2 Vaccination Between December 2020 and March 2021.

COVID-19 Italy SARS-CoV-2 breakthrough infection neutralising antibodies vaccine viral variants

Journal

Frontiers in medicine
ISSN: 2296-858X
Titre abrégé: Front Med (Lausanne)
Pays: Switzerland
ID NLM: 101648047

Informations de publication

Date de publication:
2021
Historique:
received: 15 11 2021
accepted: 22 12 2021
entrez: 7 2 2022
pubmed: 8 2 2022
medline: 8 2 2022
Statut: epublish

Résumé

Vaccines for coronavirus disease 2019 (COVID-19) are proving to be very effective in preventing severe illness; however, although rare, post-vaccine infections have been reported. The present study focuses on virological and serological features of 94 infections that occurred in Lazio Region (Central Italy) between 27 December 2020, and 30 March 2021, after one or two doses of mRNA BNT162b2 vaccine. We evaluated clinical features, virological (viral load; viral infectiousness; genomic characterisation), and serological (anti-nucleoprotein Ig; anti-Spike RBD IgG; neutralising antibodies, nAb) characteristics of 94 post-vaccine infections at the time of diagnosis. Nasopharyngeal swabs (NPSs) and serum samples were collected in the framework of the surveillance activities on SARS-CoV-2 variants established in Lazio Region (Central Italy) and analysed at the National Institute for Infectious Diseases "L. Spallanzani" in Rome. The majority (92.6%) of the post-vaccine infections showed pauci/asymptomatic or mild clinical course, with symptoms and hospitalisation rate significantly less frequent in patients infected after full vaccination course as compared to patients who received a single dose vaccine. Although differences were not statistically significant, viral loads and isolation rates were lower in NPSs from patients infected after receiving two vaccine doses as compared to patients with one dose. Most cases (84%) had nAb in serum at the time of infection diagnosis, which is a sub-group of vaccinees, were found similarly able to neutralise Alpha and Gamma variants. Asymptomatic individuals showed higher nAb titres as compared to symptomatic cases (median titre: 1:120 vs. 1:40, respectively). Finally, the proportion of post-vaccine infections attributed either to Alpha and Gamma variants was similar to the proportion observed in the contemporary unvaccinated population in the Lazio region, and mutational analysis did not reveal enrichment of a defined set of Spike protein substitutions depending on the vaccination status. Our study conducted using real-life data, emphasised the importance of monitoring vaccine breakthrough infections, through the characterisation of virological, immunological, and clinical features associated with these events, in order to tune prevention measures in the next phase of the COVID-19 pandemic.

Sections du résumé

BACKGROUND BACKGROUND
Vaccines for coronavirus disease 2019 (COVID-19) are proving to be very effective in preventing severe illness; however, although rare, post-vaccine infections have been reported. The present study focuses on virological and serological features of 94 infections that occurred in Lazio Region (Central Italy) between 27 December 2020, and 30 March 2021, after one or two doses of mRNA BNT162b2 vaccine.
METHODS METHODS
We evaluated clinical features, virological (viral load; viral infectiousness; genomic characterisation), and serological (anti-nucleoprotein Ig; anti-Spike RBD IgG; neutralising antibodies, nAb) characteristics of 94 post-vaccine infections at the time of diagnosis. Nasopharyngeal swabs (NPSs) and serum samples were collected in the framework of the surveillance activities on SARS-CoV-2 variants established in Lazio Region (Central Italy) and analysed at the National Institute for Infectious Diseases "L. Spallanzani" in Rome.
RESULTS RESULTS
The majority (92.6%) of the post-vaccine infections showed pauci/asymptomatic or mild clinical course, with symptoms and hospitalisation rate significantly less frequent in patients infected after full vaccination course as compared to patients who received a single dose vaccine. Although differences were not statistically significant, viral loads and isolation rates were lower in NPSs from patients infected after receiving two vaccine doses as compared to patients with one dose. Most cases (84%) had nAb in serum at the time of infection diagnosis, which is a sub-group of vaccinees, were found similarly able to neutralise Alpha and Gamma variants. Asymptomatic individuals showed higher nAb titres as compared to symptomatic cases (median titre: 1:120 vs. 1:40, respectively). Finally, the proportion of post-vaccine infections attributed either to Alpha and Gamma variants was similar to the proportion observed in the contemporary unvaccinated population in the Lazio region, and mutational analysis did not reveal enrichment of a defined set of Spike protein substitutions depending on the vaccination status.
CONCLUSION CONCLUSIONS
Our study conducted using real-life data, emphasised the importance of monitoring vaccine breakthrough infections, through the characterisation of virological, immunological, and clinical features associated with these events, in order to tune prevention measures in the next phase of the COVID-19 pandemic.

Identifiants

pubmed: 35127770
doi: 10.3389/fmed.2021.815870
pmc: PMC8810639
doi:

Types de publication

Journal Article

Langues

eng

Pagination

815870

Informations de copyright

Copyright © 2022 Colavita, Meschi, Gruber, Rueca, Vairo, Matusali, Lapa, Giombini, De Carli, Spaziante, Messina, Bonfiglio, Carletti, Lalle, Fabeni, Berno, Puro, Bartolini, Di Caro, Ippolito, Capobianchi and Castilletti.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Francesca Colavita (F)

National Institute for Infectious Diseases "Lazzaro Spallanzani" IRCCS, Roma, Italy.

Silvia Meschi (S)

National Institute for Infectious Diseases "Lazzaro Spallanzani" IRCCS, Roma, Italy.

Cesare Ernesto Maria Gruber (CEM)

National Institute for Infectious Diseases "Lazzaro Spallanzani" IRCCS, Roma, Italy.

Martina Rueca (M)

National Institute for Infectious Diseases "Lazzaro Spallanzani" IRCCS, Roma, Italy.

Francesco Vairo (F)

National Institute for Infectious Diseases "Lazzaro Spallanzani" IRCCS, Roma, Italy.

Giulia Matusali (G)

National Institute for Infectious Diseases "Lazzaro Spallanzani" IRCCS, Roma, Italy.

Daniele Lapa (D)

National Institute for Infectious Diseases "Lazzaro Spallanzani" IRCCS, Roma, Italy.

Emanuela Giombini (E)

National Institute for Infectious Diseases "Lazzaro Spallanzani" IRCCS, Roma, Italy.

Gabriella De Carli (G)

National Institute for Infectious Diseases "Lazzaro Spallanzani" IRCCS, Roma, Italy.

Martina Spaziante (M)

National Institute for Infectious Diseases "Lazzaro Spallanzani" IRCCS, Roma, Italy.

Francesco Messina (F)

National Institute for Infectious Diseases "Lazzaro Spallanzani" IRCCS, Roma, Italy.

Giulia Bonfiglio (G)

National Institute for Infectious Diseases "Lazzaro Spallanzani" IRCCS, Roma, Italy.

Fabrizio Carletti (F)

National Institute for Infectious Diseases "Lazzaro Spallanzani" IRCCS, Roma, Italy.

Eleonora Lalle (E)

National Institute for Infectious Diseases "Lazzaro Spallanzani" IRCCS, Roma, Italy.

Lavinia Fabeni (L)

National Institute for Infectious Diseases "Lazzaro Spallanzani" IRCCS, Roma, Italy.

Giulia Berno (G)

National Institute for Infectious Diseases "Lazzaro Spallanzani" IRCCS, Roma, Italy.

Vincenzo Puro (V)

National Institute for Infectious Diseases "Lazzaro Spallanzani" IRCCS, Roma, Italy.

Barbara Bartolini (B)

National Institute for Infectious Diseases "Lazzaro Spallanzani" IRCCS, Roma, Italy.

Antonino Di Caro (A)

National Institute for Infectious Diseases "Lazzaro Spallanzani" IRCCS, Roma, Italy.
Unicamillus, International Medical University, Roma, Italy.

Giuseppe Ippolito (G)

National Institute for Infectious Diseases "Lazzaro Spallanzani" IRCCS, Roma, Italy.

Maria Rosaria Capobianchi (MR)

National Institute for Infectious Diseases "Lazzaro Spallanzani" IRCCS, Roma, Italy.
Unicamillus, International Medical University, Roma, Italy.

Concetta Castilletti (C)

National Institute for Infectious Diseases "Lazzaro Spallanzani" IRCCS, Roma, Italy.

Classifications MeSH