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Long-term immunogenicity in previously vaccinated healthcare workers with inactivated virus vaccine after SARS-CoV-2 infection or booster vaccination

Immunity against SARS-CoV-2 infection in vaccinated individuals varies based on the vaccine type, duration after vaccination or infection, and SARS-CoV-2 variant type. We conducted a prospective observational study to evaluate the immunogenicity of a booster vaccination with AZD1222 after two doses...

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Autores principales: Terbsiri, Varalee, Putcharoen, Opass, Suwanpimolkul, Gompol, Jantarabenjakul, Watsamon, Wacharapluesadee, Supaporn, Champa, Nuntana, Thippamom, Nattakarn, Paitoonpong, Leilani
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10281697/
https://www.ncbi.nlm.nih.gov/pubmed/37361052
http://dx.doi.org/10.1016/j.jvacx.2023.100334
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author Terbsiri, Varalee
Putcharoen, Opass
Suwanpimolkul, Gompol
Jantarabenjakul, Watsamon
Wacharapluesadee, Supaporn
Champa, Nuntana
Thippamom, Nattakarn
Paitoonpong, Leilani
author_facet Terbsiri, Varalee
Putcharoen, Opass
Suwanpimolkul, Gompol
Jantarabenjakul, Watsamon
Wacharapluesadee, Supaporn
Champa, Nuntana
Thippamom, Nattakarn
Paitoonpong, Leilani
author_sort Terbsiri, Varalee
collection PubMed
description Immunity against SARS-CoV-2 infection in vaccinated individuals varies based on the vaccine type, duration after vaccination or infection, and SARS-CoV-2 variant type. We conducted a prospective observational study to evaluate the immunogenicity of a booster vaccination with AZD1222 after two doses of CoronaVac (booster group) compared to individuals who had SARS-CoV-2 infection after receiving two doses of CoronaVac (infection group). We used a surrogate virus neutralization test (sVNT) to evaluate immunity against wild-type and Omicron variant (BA.1) at 3 and 6 months after infection or booster dose. Of the 89 participants, 41 were in the infection group, and 48 were in the booster group. At 3 months post-infection or booster vaccination, the median (IQR) sVNT against wild-type was 97.87 % (97.57–97.93 %) and 97.65 % (95.38–98.00 %), p = 0.66, respectively, while the sVNT against Omicron was 18.8 % (0–47.10 %) and 24.46 (11.69–35.47 %), p = 0.72 respectively. At 6 months, the median (IQR) sVNT against wild-type was 97.68 % (95.86–97.92 %) in the infection group, higher than 94.7 % (95.38–98.00 %) in the booster group (p = 0.03). Results showed no significant difference in immunity against wild-type and Omicron at 3 months between the two groups. However, the infection group exhibited better immunity than the booster group at 6 months.
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spelling pubmed-102816972023-06-21 Long-term immunogenicity in previously vaccinated healthcare workers with inactivated virus vaccine after SARS-CoV-2 infection or booster vaccination Terbsiri, Varalee Putcharoen, Opass Suwanpimolkul, Gompol Jantarabenjakul, Watsamon Wacharapluesadee, Supaporn Champa, Nuntana Thippamom, Nattakarn Paitoonpong, Leilani Vaccine X Regular paper Immunity against SARS-CoV-2 infection in vaccinated individuals varies based on the vaccine type, duration after vaccination or infection, and SARS-CoV-2 variant type. We conducted a prospective observational study to evaluate the immunogenicity of a booster vaccination with AZD1222 after two doses of CoronaVac (booster group) compared to individuals who had SARS-CoV-2 infection after receiving two doses of CoronaVac (infection group). We used a surrogate virus neutralization test (sVNT) to evaluate immunity against wild-type and Omicron variant (BA.1) at 3 and 6 months after infection or booster dose. Of the 89 participants, 41 were in the infection group, and 48 were in the booster group. At 3 months post-infection or booster vaccination, the median (IQR) sVNT against wild-type was 97.87 % (97.57–97.93 %) and 97.65 % (95.38–98.00 %), p = 0.66, respectively, while the sVNT against Omicron was 18.8 % (0–47.10 %) and 24.46 (11.69–35.47 %), p = 0.72 respectively. At 6 months, the median (IQR) sVNT against wild-type was 97.68 % (95.86–97.92 %) in the infection group, higher than 94.7 % (95.38–98.00 %) in the booster group (p = 0.03). Results showed no significant difference in immunity against wild-type and Omicron at 3 months between the two groups. However, the infection group exhibited better immunity than the booster group at 6 months. Elsevier 2023-06-20 /pmc/articles/PMC10281697/ /pubmed/37361052 http://dx.doi.org/10.1016/j.jvacx.2023.100334 Text en © 2023 The Author(s) 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 Regular paper
Terbsiri, Varalee
Putcharoen, Opass
Suwanpimolkul, Gompol
Jantarabenjakul, Watsamon
Wacharapluesadee, Supaporn
Champa, Nuntana
Thippamom, Nattakarn
Paitoonpong, Leilani
Long-term immunogenicity in previously vaccinated healthcare workers with inactivated virus vaccine after SARS-CoV-2 infection or booster vaccination
title Long-term immunogenicity in previously vaccinated healthcare workers with inactivated virus vaccine after SARS-CoV-2 infection or booster vaccination
title_full Long-term immunogenicity in previously vaccinated healthcare workers with inactivated virus vaccine after SARS-CoV-2 infection or booster vaccination
title_fullStr Long-term immunogenicity in previously vaccinated healthcare workers with inactivated virus vaccine after SARS-CoV-2 infection or booster vaccination
title_full_unstemmed Long-term immunogenicity in previously vaccinated healthcare workers with inactivated virus vaccine after SARS-CoV-2 infection or booster vaccination
title_short Long-term immunogenicity in previously vaccinated healthcare workers with inactivated virus vaccine after SARS-CoV-2 infection or booster vaccination
title_sort long-term immunogenicity in previously vaccinated healthcare workers with inactivated virus vaccine after sars-cov-2 infection or booster vaccination
topic Regular paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10281697/
https://www.ncbi.nlm.nih.gov/pubmed/37361052
http://dx.doi.org/10.1016/j.jvacx.2023.100334
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