Investigating the impact of prior COVID-19 on IgG antibody and interferon γ responses after BBIBP-CorV vaccination in a disease endemic population: a prospective observational study

Detalhes bibliográficos
Autor(a) principal: Hasan, Zahra
Data de Publicação: 2023
Outros Autores: Masood, Kiran Iqbal, Qaiser, Shama, Khan, Erum, Hussain, Areeba, Ghous, Zara, Khan, Unab, Yameen, Maliha, Hassan, Imran, Nasir, Muhammad Imran, Qazi, Muhammad Farrukh, Memon, Haris Ali, Ali, Shiza, Baloch, Sadaf, Bhutta, Zulfiqar A., Veldhoen, Marc, Simas, J. Pedro, Mahmood, Syed Faisal, Ghias, Kulsoom, Hussain, Rabia
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.14/42685
Resumo: Background and Aims: COVID-19 vaccinations have reduced morbidity and mortality from the disease. Antibodies against severe acute respiratory syndrome coronavirus 2 (SARS‑CoV‑2) have been associated with immune protection. Seroprevalence studies revealed high immunoglobulin G (IgG) antibody levels to SARS-CoV-2 in the Pakistani population before vaccinations. We investigated the effect of BBIBP-CorV vaccination on circulating IgG antibodies and interferon (IFN)-γ from T cells measured in a cohort of healthy individuals, with respect to age, gender, and history of COVID-19. Methods: The study was conducted between April and October 2021. BBIBP-CorV vaccinated participants were followed up to 24 weeks. Antibodies to SARS-CoV-2 Spike protein and its receptor-binding domain (RBD) were measured. IFNγ secreted by whole blood stimulation of Spike protein and extended genome antigens was determined. Results: Study participants with a history of prior COVID-19 displayed a higher magnitude of IgG antibodies to Spike and RBD. IgG seropositivity was greater in those with prior COVID-19, aged 50 years or younger and in females. At 24 weeks after vaccination, 37.4% of participants showed IFN-γ responses to SARS-CoV-2 antigens. T cell IFN-γ release was higher in those with prior COVID-19 and those aged 50 years or less. Highest IFN-γ release was observed to extended genome antigens in individuals both with and without prior COVID-19. Conclusion: We found that IgG seropositivity to both Spike and RBD was affected by prior COVID-19, age and gender. Importantly, seropositive responses persisted up to 24 weeks after vaccination. Persistence of vaccine induced IgG antibodies may be linked to the high seroprevalence observed earlier in unvaccinated individuals. Increased T cell reactivity to Spike and extended genome antigens reflects cellular activation induced by BBIBP-CorV. COVID-19 vaccination may have longer lasting immune responses in populations with a higher seroprevalence. These data inform on vaccination booster policies for high-risk groups.
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spelling Investigating the impact of prior COVID-19 on IgG antibody and interferon γ responses after BBIBP-CorV vaccination in a disease endemic population: a prospective observational studyCOVID-19Immunoglobulin GInterferonsT-lymphocytesVaccinationBackground and Aims: COVID-19 vaccinations have reduced morbidity and mortality from the disease. Antibodies against severe acute respiratory syndrome coronavirus 2 (SARS‑CoV‑2) have been associated with immune protection. Seroprevalence studies revealed high immunoglobulin G (IgG) antibody levels to SARS-CoV-2 in the Pakistani population before vaccinations. We investigated the effect of BBIBP-CorV vaccination on circulating IgG antibodies and interferon (IFN)-γ from T cells measured in a cohort of healthy individuals, with respect to age, gender, and history of COVID-19. Methods: The study was conducted between April and October 2021. BBIBP-CorV vaccinated participants were followed up to 24 weeks. Antibodies to SARS-CoV-2 Spike protein and its receptor-binding domain (RBD) were measured. IFNγ secreted by whole blood stimulation of Spike protein and extended genome antigens was determined. Results: Study participants with a history of prior COVID-19 displayed a higher magnitude of IgG antibodies to Spike and RBD. IgG seropositivity was greater in those with prior COVID-19, aged 50 years or younger and in females. At 24 weeks after vaccination, 37.4% of participants showed IFN-γ responses to SARS-CoV-2 antigens. T cell IFN-γ release was higher in those with prior COVID-19 and those aged 50 years or less. Highest IFN-γ release was observed to extended genome antigens in individuals both with and without prior COVID-19. Conclusion: We found that IgG seropositivity to both Spike and RBD was affected by prior COVID-19, age and gender. Importantly, seropositive responses persisted up to 24 weeks after vaccination. Persistence of vaccine induced IgG antibodies may be linked to the high seroprevalence observed earlier in unvaccinated individuals. Increased T cell reactivity to Spike and extended genome antigens reflects cellular activation induced by BBIBP-CorV. COVID-19 vaccination may have longer lasting immune responses in populations with a higher seroprevalence. These data inform on vaccination booster policies for high-risk groups.Veritati - Repositório Institucional da Universidade Católica PortuguesaHasan, ZahraMasood, Kiran IqbalQaiser, ShamaKhan, ErumHussain, AreebaGhous, ZaraKhan, UnabYameen, MalihaHassan, ImranNasir, Muhammad ImranQazi, Muhammad FarrukhMemon, Haris AliAli, ShizaBaloch, SadafBhutta, Zulfiqar A.Veldhoen, MarcSimas, J. PedroMahmood, Syed FaisalGhias, KulsoomHussain, Rabia2023-09-27T16:18:43Z20232023-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.14/42685eng2398-883510.1002/hsr2.15218517004446737692793001065207000001info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-10-10T01:40:59Zoai:repositorio.ucp.pt:10400.14/42685Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:31:58.535380Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Investigating the impact of prior COVID-19 on IgG antibody and interferon γ responses after BBIBP-CorV vaccination in a disease endemic population: a prospective observational study
title Investigating the impact of prior COVID-19 on IgG antibody and interferon γ responses after BBIBP-CorV vaccination in a disease endemic population: a prospective observational study
spellingShingle Investigating the impact of prior COVID-19 on IgG antibody and interferon γ responses after BBIBP-CorV vaccination in a disease endemic population: a prospective observational study
Hasan, Zahra
COVID-19
Immunoglobulin G
Interferons
T-lymphocytes
Vaccination
title_short Investigating the impact of prior COVID-19 on IgG antibody and interferon γ responses after BBIBP-CorV vaccination in a disease endemic population: a prospective observational study
title_full Investigating the impact of prior COVID-19 on IgG antibody and interferon γ responses after BBIBP-CorV vaccination in a disease endemic population: a prospective observational study
title_fullStr Investigating the impact of prior COVID-19 on IgG antibody and interferon γ responses after BBIBP-CorV vaccination in a disease endemic population: a prospective observational study
title_full_unstemmed Investigating the impact of prior COVID-19 on IgG antibody and interferon γ responses after BBIBP-CorV vaccination in a disease endemic population: a prospective observational study
title_sort Investigating the impact of prior COVID-19 on IgG antibody and interferon γ responses after BBIBP-CorV vaccination in a disease endemic population: a prospective observational study
author Hasan, Zahra
author_facet Hasan, Zahra
Masood, Kiran Iqbal
Qaiser, Shama
Khan, Erum
Hussain, Areeba
Ghous, Zara
Khan, Unab
Yameen, Maliha
Hassan, Imran
Nasir, Muhammad Imran
Qazi, Muhammad Farrukh
Memon, Haris Ali
Ali, Shiza
Baloch, Sadaf
Bhutta, Zulfiqar A.
Veldhoen, Marc
Simas, J. Pedro
Mahmood, Syed Faisal
Ghias, Kulsoom
Hussain, Rabia
author_role author
author2 Masood, Kiran Iqbal
Qaiser, Shama
Khan, Erum
Hussain, Areeba
Ghous, Zara
Khan, Unab
Yameen, Maliha
Hassan, Imran
Nasir, Muhammad Imran
Qazi, Muhammad Farrukh
Memon, Haris Ali
Ali, Shiza
Baloch, Sadaf
Bhutta, Zulfiqar A.
Veldhoen, Marc
Simas, J. Pedro
Mahmood, Syed Faisal
Ghias, Kulsoom
Hussain, Rabia
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Veritati - Repositório Institucional da Universidade Católica Portuguesa
dc.contributor.author.fl_str_mv Hasan, Zahra
Masood, Kiran Iqbal
Qaiser, Shama
Khan, Erum
Hussain, Areeba
Ghous, Zara
Khan, Unab
Yameen, Maliha
Hassan, Imran
Nasir, Muhammad Imran
Qazi, Muhammad Farrukh
Memon, Haris Ali
Ali, Shiza
Baloch, Sadaf
Bhutta, Zulfiqar A.
Veldhoen, Marc
Simas, J. Pedro
Mahmood, Syed Faisal
Ghias, Kulsoom
Hussain, Rabia
dc.subject.por.fl_str_mv COVID-19
Immunoglobulin G
Interferons
T-lymphocytes
Vaccination
topic COVID-19
Immunoglobulin G
Interferons
T-lymphocytes
Vaccination
description Background and Aims: COVID-19 vaccinations have reduced morbidity and mortality from the disease. Antibodies against severe acute respiratory syndrome coronavirus 2 (SARS‑CoV‑2) have been associated with immune protection. Seroprevalence studies revealed high immunoglobulin G (IgG) antibody levels to SARS-CoV-2 in the Pakistani population before vaccinations. We investigated the effect of BBIBP-CorV vaccination on circulating IgG antibodies and interferon (IFN)-γ from T cells measured in a cohort of healthy individuals, with respect to age, gender, and history of COVID-19. Methods: The study was conducted between April and October 2021. BBIBP-CorV vaccinated participants were followed up to 24 weeks. Antibodies to SARS-CoV-2 Spike protein and its receptor-binding domain (RBD) were measured. IFNγ secreted by whole blood stimulation of Spike protein and extended genome antigens was determined. Results: Study participants with a history of prior COVID-19 displayed a higher magnitude of IgG antibodies to Spike and RBD. IgG seropositivity was greater in those with prior COVID-19, aged 50 years or younger and in females. At 24 weeks after vaccination, 37.4% of participants showed IFN-γ responses to SARS-CoV-2 antigens. T cell IFN-γ release was higher in those with prior COVID-19 and those aged 50 years or less. Highest IFN-γ release was observed to extended genome antigens in individuals both with and without prior COVID-19. Conclusion: We found that IgG seropositivity to both Spike and RBD was affected by prior COVID-19, age and gender. Importantly, seropositive responses persisted up to 24 weeks after vaccination. Persistence of vaccine induced IgG antibodies may be linked to the high seroprevalence observed earlier in unvaccinated individuals. Increased T cell reactivity to Spike and extended genome antigens reflects cellular activation induced by BBIBP-CorV. COVID-19 vaccination may have longer lasting immune responses in populations with a higher seroprevalence. These data inform on vaccination booster policies for high-risk groups.
publishDate 2023
dc.date.none.fl_str_mv 2023-09-27T16:18:43Z
2023
2023-01-01T00:00:00Z
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dc.language.iso.fl_str_mv eng
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dc.relation.none.fl_str_mv 2398-8835
10.1002/hsr2.1521
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