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Prevalence of SARS-CoV-2 antibodies after the Omicron surge, Kingston, Jamaica, 2022

A cross-sectional SARS-CoV-2 serosurvey was conducted after the Omicron surge in Jamaica using 1,540 samples collected during March – May 2022 from persons attending antenatal, STI and non-communicable diseases clinics in Kingston, Jamaica. SARS-CoV-2 spike receptor binding domain (RBD) and/or nucle...

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Autores principales: Anzinger, Joshua J., Cameron-McDermott, Suzette M., Phillips, Yakima Z.R., Mendoza, Leshawn, Anderson, Mark, Cloherty, Gavin, Strachan-Johnson, Susan, Lindo, John F., Figueroa, J. Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Author(s). Published by Elsevier Ltd. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9671617/
https://www.ncbi.nlm.nih.gov/pubmed/36415687
http://dx.doi.org/10.1016/j.jcvp.2022.100124
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author Anzinger, Joshua J.
Cameron-McDermott, Suzette M.
Phillips, Yakima Z.R.
Mendoza, Leshawn
Anderson, Mark
Cloherty, Gavin
Strachan-Johnson, Susan
Lindo, John F.
Figueroa, J. Peter
author_facet Anzinger, Joshua J.
Cameron-McDermott, Suzette M.
Phillips, Yakima Z.R.
Mendoza, Leshawn
Anderson, Mark
Cloherty, Gavin
Strachan-Johnson, Susan
Lindo, John F.
Figueroa, J. Peter
author_sort Anzinger, Joshua J.
collection PubMed
description A cross-sectional SARS-CoV-2 serosurvey was conducted after the Omicron surge in Jamaica using 1,540 samples collected during March – May 2022 from persons attending antenatal, STI and non-communicable diseases clinics in Kingston, Jamaica. SARS-CoV-2 spike receptor binding domain (RBD) and/or nucleocapsid IgG antibodies were detected for 88.4% of the study population, with 77.0% showing evidence of previous SARS-CoV-2 infection. Of persons previously infected with SARS-CoV-2 and/or with COVID-19 vaccination, 9.6% were negative for spike RBD IgG, most of which were unvaccinated previously infected persons. Amongst unvaccinated previously infected people, age was associated with testing spike RBD IgG negative. When considering all samples, median spike RBD IgG levels were 131.6 BAU/mL for unvaccinated persons with serological evidence of past infection, 90.3 BAU/mL for vaccinated persons without serological evidence of past infection, and 896.1 BAU/mL for vaccinated persons with serological evidence of past infection. Our study of the first reported SARS-CoV-2 serosurvey in Jamaica shows extensive SARS-CoV-2 population immunity, identifies a substantial portion of the population lacking spike RBD IgG, and provides additional evidence for increasing COVID-19 vaccine coverage in Jamaica.
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spelling pubmed-96716172022-11-18 Prevalence of SARS-CoV-2 antibodies after the Omicron surge, Kingston, Jamaica, 2022 Anzinger, Joshua J. Cameron-McDermott, Suzette M. Phillips, Yakima Z.R. Mendoza, Leshawn Anderson, Mark Cloherty, Gavin Strachan-Johnson, Susan Lindo, John F. Figueroa, J. Peter J Clin Virol Plus Article A cross-sectional SARS-CoV-2 serosurvey was conducted after the Omicron surge in Jamaica using 1,540 samples collected during March – May 2022 from persons attending antenatal, STI and non-communicable diseases clinics in Kingston, Jamaica. SARS-CoV-2 spike receptor binding domain (RBD) and/or nucleocapsid IgG antibodies were detected for 88.4% of the study population, with 77.0% showing evidence of previous SARS-CoV-2 infection. Of persons previously infected with SARS-CoV-2 and/or with COVID-19 vaccination, 9.6% were negative for spike RBD IgG, most of which were unvaccinated previously infected persons. Amongst unvaccinated previously infected people, age was associated with testing spike RBD IgG negative. When considering all samples, median spike RBD IgG levels were 131.6 BAU/mL for unvaccinated persons with serological evidence of past infection, 90.3 BAU/mL for vaccinated persons without serological evidence of past infection, and 896.1 BAU/mL for vaccinated persons with serological evidence of past infection. Our study of the first reported SARS-CoV-2 serosurvey in Jamaica shows extensive SARS-CoV-2 population immunity, identifies a substantial portion of the population lacking spike RBD IgG, and provides additional evidence for increasing COVID-19 vaccine coverage in Jamaica. The Author(s). Published by Elsevier Ltd. 2022-11 2022-11-17 /pmc/articles/PMC9671617/ /pubmed/36415687 http://dx.doi.org/10.1016/j.jcvp.2022.100124 Text en © 2022 The Author(s) Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Anzinger, Joshua J.
Cameron-McDermott, Suzette M.
Phillips, Yakima Z.R.
Mendoza, Leshawn
Anderson, Mark
Cloherty, Gavin
Strachan-Johnson, Susan
Lindo, John F.
Figueroa, J. Peter
Prevalence of SARS-CoV-2 antibodies after the Omicron surge, Kingston, Jamaica, 2022
title Prevalence of SARS-CoV-2 antibodies after the Omicron surge, Kingston, Jamaica, 2022
title_full Prevalence of SARS-CoV-2 antibodies after the Omicron surge, Kingston, Jamaica, 2022
title_fullStr Prevalence of SARS-CoV-2 antibodies after the Omicron surge, Kingston, Jamaica, 2022
title_full_unstemmed Prevalence of SARS-CoV-2 antibodies after the Omicron surge, Kingston, Jamaica, 2022
title_short Prevalence of SARS-CoV-2 antibodies after the Omicron surge, Kingston, Jamaica, 2022
title_sort prevalence of sars-cov-2 antibodies after the omicron surge, kingston, jamaica, 2022
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9671617/
https://www.ncbi.nlm.nih.gov/pubmed/36415687
http://dx.doi.org/10.1016/j.jcvp.2022.100124
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