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Timing and implications for immune response to vaccine in SARS-CoV-2 breakthrough infections
COVID-19 vaccines elicit a strong anti-S antibodies response. We aim to describe antibody titers in peri-vaccination SARS-CoV-2 infections. This is a retrospective longitudinal single-cohort study. Serological tests were performed at the time of the first SARS-CoV-2 vaccine dose (T0) and 60 (T1), 12...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10122568/ https://www.ncbi.nlm.nih.gov/pubmed/37152764 http://dx.doi.org/10.1016/j.isci.2023.106716 |
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author | Arsuffi, Stefania Sansone, Emanuele Focà, Emanuele Storti, Samuele Diaferia, Teresa Bonfanti, Carlo Terlenghi, Luigina Caruso, Arnaldo Sala, Emma Castelli, Francesco De Palma, Giuseppe Quiros-Roldan, Eugenia |
author_facet | Arsuffi, Stefania Sansone, Emanuele Focà, Emanuele Storti, Samuele Diaferia, Teresa Bonfanti, Carlo Terlenghi, Luigina Caruso, Arnaldo Sala, Emma Castelli, Francesco De Palma, Giuseppe Quiros-Roldan, Eugenia |
author_sort | Arsuffi, Stefania |
collection | PubMed |
description | COVID-19 vaccines elicit a strong anti-S antibodies response. We aim to describe antibody titers in peri-vaccination SARS-CoV-2 infections. This is a retrospective longitudinal single-cohort study. Serological tests were performed at the time of the first SARS-CoV-2 vaccine dose (T0) and 60 (T1), 120 (T2), and 240 (T3) days after. The study included 4,682 subjects. Group A had the infection without an anti-S Ig response. Group B and C seroconverted for anti-N Ig between T0 and T1 and between T1 and T2, respectively. Group D was persistently anti-N Ig negative. Group B showed an initial sub-optimal response, reaching the highest titer at T3. Those who received the second dose 120 days after the infection had higher titers compared to those who received it 21 days after the first dose. The immune response depends on the number and the timing of vaccine doses, highlighting the need for a more personalized approach to vaccination. |
format | Online Article Text |
id | pubmed-10122568 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-101225682023-04-24 Timing and implications for immune response to vaccine in SARS-CoV-2 breakthrough infections Arsuffi, Stefania Sansone, Emanuele Focà, Emanuele Storti, Samuele Diaferia, Teresa Bonfanti, Carlo Terlenghi, Luigina Caruso, Arnaldo Sala, Emma Castelli, Francesco De Palma, Giuseppe Quiros-Roldan, Eugenia iScience Article COVID-19 vaccines elicit a strong anti-S antibodies response. We aim to describe antibody titers in peri-vaccination SARS-CoV-2 infections. This is a retrospective longitudinal single-cohort study. Serological tests were performed at the time of the first SARS-CoV-2 vaccine dose (T0) and 60 (T1), 120 (T2), and 240 (T3) days after. The study included 4,682 subjects. Group A had the infection without an anti-S Ig response. Group B and C seroconverted for anti-N Ig between T0 and T1 and between T1 and T2, respectively. Group D was persistently anti-N Ig negative. Group B showed an initial sub-optimal response, reaching the highest titer at T3. Those who received the second dose 120 days after the infection had higher titers compared to those who received it 21 days after the first dose. The immune response depends on the number and the timing of vaccine doses, highlighting the need for a more personalized approach to vaccination. Elsevier 2023-04-23 /pmc/articles/PMC10122568/ /pubmed/37152764 http://dx.doi.org/10.1016/j.isci.2023.106716 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Arsuffi, Stefania Sansone, Emanuele Focà, Emanuele Storti, Samuele Diaferia, Teresa Bonfanti, Carlo Terlenghi, Luigina Caruso, Arnaldo Sala, Emma Castelli, Francesco De Palma, Giuseppe Quiros-Roldan, Eugenia Timing and implications for immune response to vaccine in SARS-CoV-2 breakthrough infections |
title | Timing and implications for immune response to vaccine in SARS-CoV-2 breakthrough infections |
title_full | Timing and implications for immune response to vaccine in SARS-CoV-2 breakthrough infections |
title_fullStr | Timing and implications for immune response to vaccine in SARS-CoV-2 breakthrough infections |
title_full_unstemmed | Timing and implications for immune response to vaccine in SARS-CoV-2 breakthrough infections |
title_short | Timing and implications for immune response to vaccine in SARS-CoV-2 breakthrough infections |
title_sort | timing and implications for immune response to vaccine in sars-cov-2 breakthrough infections |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10122568/ https://www.ncbi.nlm.nih.gov/pubmed/37152764 http://dx.doi.org/10.1016/j.isci.2023.106716 |
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