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Increased Seroprevalence and Improved Antibody Responses Following Third Primary SARS-CoV-2 Immunisation: An Update From the COV-AD Study

BACKGROUND: Patients with primary and secondary antibody deficiency are vulnerable to COVID-19 and demonstrate diminished responses following two-dose SARS-CoV-2 vaccine schedules. Third primary vaccinations have been deployed to enhance their humoral and cellular immunity. OBJECTIVES: To determine...

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Autores principales: Shields, Adrian M., Faustini, Sian E., Hill, Harriet J., Al-Taei, Saly, Tanner, Chloe, Ashford, Fiona, Workman, Sarita, Moreira, Fernando, Verma, Nisha, Wagg, Hollie, Heritage, Gail, Campton, Naomi, Stamataki, Zania, Drayson, Mark T., Klenerman, Paul, Thaventhiran, James E. D., Elkhalifa, Shuayb, Goddard, Sarah, Johnston, Sarah, Huissoon, Aarnoud, Bethune, Claire, Elcombe, Suzanne, Lowe, David M., Patel, Smita Y., Savic, Sinisa, Richter, Alex G., Burns, Siobhan O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9201027/
https://www.ncbi.nlm.nih.gov/pubmed/35720400
http://dx.doi.org/10.3389/fimmu.2022.912571
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author Shields, Adrian M.
Faustini, Sian E.
Hill, Harriet J.
Al-Taei, Saly
Tanner, Chloe
Ashford, Fiona
Workman, Sarita
Moreira, Fernando
Verma, Nisha
Wagg, Hollie
Heritage, Gail
Campton, Naomi
Stamataki, Zania
Drayson, Mark T.
Klenerman, Paul
Thaventhiran, James E. D.
Elkhalifa, Shuayb
Goddard, Sarah
Johnston, Sarah
Huissoon, Aarnoud
Bethune, Claire
Elcombe, Suzanne
Lowe, David M.
Patel, Smita Y.
Savic, Sinisa
Richter, Alex G.
Burns, Siobhan O.
author_facet Shields, Adrian M.
Faustini, Sian E.
Hill, Harriet J.
Al-Taei, Saly
Tanner, Chloe
Ashford, Fiona
Workman, Sarita
Moreira, Fernando
Verma, Nisha
Wagg, Hollie
Heritage, Gail
Campton, Naomi
Stamataki, Zania
Drayson, Mark T.
Klenerman, Paul
Thaventhiran, James E. D.
Elkhalifa, Shuayb
Goddard, Sarah
Johnston, Sarah
Huissoon, Aarnoud
Bethune, Claire
Elcombe, Suzanne
Lowe, David M.
Patel, Smita Y.
Savic, Sinisa
Richter, Alex G.
Burns, Siobhan O.
author_sort Shields, Adrian M.
collection PubMed
description BACKGROUND: Patients with primary and secondary antibody deficiency are vulnerable to COVID-19 and demonstrate diminished responses following two-dose SARS-CoV-2 vaccine schedules. Third primary vaccinations have been deployed to enhance their humoral and cellular immunity. OBJECTIVES: To determine the immunogenicity of the third primary SARS-CoV-2 immunisation in a heterogeneous cohort of patients with antibody deficiency. METHODS: Participants enrolled in the COV-AD study were sampled before and after their third vaccine dose. Serological and cellular responses were determined using ELISA, live-virus neutralisation and ELISPOT assays. RESULTS: Following a two-dose schedule, 100% of healthy controls mounted a serological response to SARS-CoV-2 vaccination, however, 38.6% of individuals with antibody deficiency remained seronegative. A third primary SARS-CoV-2 vaccine significantly increased anti-spike glycoprotein antibody seroprevalence from 61.4% to 76.0%, the magnitude of the antibody response, its neutralising capacity and induced seroconversion in individuals who were seronegative after two vaccine doses. Vaccine-induced serological responses were broadly cross-reactive against the SARS-CoV-2 B.1.1.529 variant of concern, however, seroprevalence and antibody levels remained significantly lower than healthy controls. No differences in serological responses were observed between individuals who received AstraZeneca ChAdOx1 nCoV-19 and Pfizer BioNTech 162b2 during their initial two-dose vaccine schedule. SARS-CoV-2 infection-naive participants who had received a heterologous vaccine as a third dose were significantly more likely to have a detectable T cell response following their third vaccine dose (61.5% vs 11.1%). CONCLUSION: These data support the widespread use of third primary immunisations to enhance humoral immunity against SARS-CoV-2 in individuals with antibody deficiency.
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spelling pubmed-92010272022-06-17 Increased Seroprevalence and Improved Antibody Responses Following Third Primary SARS-CoV-2 Immunisation: An Update From the COV-AD Study Shields, Adrian M. Faustini, Sian E. Hill, Harriet J. Al-Taei, Saly Tanner, Chloe Ashford, Fiona Workman, Sarita Moreira, Fernando Verma, Nisha Wagg, Hollie Heritage, Gail Campton, Naomi Stamataki, Zania Drayson, Mark T. Klenerman, Paul Thaventhiran, James E. D. Elkhalifa, Shuayb Goddard, Sarah Johnston, Sarah Huissoon, Aarnoud Bethune, Claire Elcombe, Suzanne Lowe, David M. Patel, Smita Y. Savic, Sinisa Richter, Alex G. Burns, Siobhan O. Front Immunol Immunology BACKGROUND: Patients with primary and secondary antibody deficiency are vulnerable to COVID-19 and demonstrate diminished responses following two-dose SARS-CoV-2 vaccine schedules. Third primary vaccinations have been deployed to enhance their humoral and cellular immunity. OBJECTIVES: To determine the immunogenicity of the third primary SARS-CoV-2 immunisation in a heterogeneous cohort of patients with antibody deficiency. METHODS: Participants enrolled in the COV-AD study were sampled before and after their third vaccine dose. Serological and cellular responses were determined using ELISA, live-virus neutralisation and ELISPOT assays. RESULTS: Following a two-dose schedule, 100% of healthy controls mounted a serological response to SARS-CoV-2 vaccination, however, 38.6% of individuals with antibody deficiency remained seronegative. A third primary SARS-CoV-2 vaccine significantly increased anti-spike glycoprotein antibody seroprevalence from 61.4% to 76.0%, the magnitude of the antibody response, its neutralising capacity and induced seroconversion in individuals who were seronegative after two vaccine doses. Vaccine-induced serological responses were broadly cross-reactive against the SARS-CoV-2 B.1.1.529 variant of concern, however, seroprevalence and antibody levels remained significantly lower than healthy controls. No differences in serological responses were observed between individuals who received AstraZeneca ChAdOx1 nCoV-19 and Pfizer BioNTech 162b2 during their initial two-dose vaccine schedule. SARS-CoV-2 infection-naive participants who had received a heterologous vaccine as a third dose were significantly more likely to have a detectable T cell response following their third vaccine dose (61.5% vs 11.1%). CONCLUSION: These data support the widespread use of third primary immunisations to enhance humoral immunity against SARS-CoV-2 in individuals with antibody deficiency. Frontiers Media S.A. 2022-06-02 /pmc/articles/PMC9201027/ /pubmed/35720400 http://dx.doi.org/10.3389/fimmu.2022.912571 Text en Copyright © 2022 Shields, Faustini, Hill, Al-Taei, Tanner, Ashford, Workman, Moreira, Verma, Wagg, Heritage, Campton, Stamataki, Drayson, Klenerman, Thaventhiran, Elkhalifa, Goddard, Johnston, Huissoon, Bethune, Elcombe, Lowe, Patel, Savic, Richter, Burns and the COV-AD consortium https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Shields, Adrian M.
Faustini, Sian E.
Hill, Harriet J.
Al-Taei, Saly
Tanner, Chloe
Ashford, Fiona
Workman, Sarita
Moreira, Fernando
Verma, Nisha
Wagg, Hollie
Heritage, Gail
Campton, Naomi
Stamataki, Zania
Drayson, Mark T.
Klenerman, Paul
Thaventhiran, James E. D.
Elkhalifa, Shuayb
Goddard, Sarah
Johnston, Sarah
Huissoon, Aarnoud
Bethune, Claire
Elcombe, Suzanne
Lowe, David M.
Patel, Smita Y.
Savic, Sinisa
Richter, Alex G.
Burns, Siobhan O.
Increased Seroprevalence and Improved Antibody Responses Following Third Primary SARS-CoV-2 Immunisation: An Update From the COV-AD Study
title Increased Seroprevalence and Improved Antibody Responses Following Third Primary SARS-CoV-2 Immunisation: An Update From the COV-AD Study
title_full Increased Seroprevalence and Improved Antibody Responses Following Third Primary SARS-CoV-2 Immunisation: An Update From the COV-AD Study
title_fullStr Increased Seroprevalence and Improved Antibody Responses Following Third Primary SARS-CoV-2 Immunisation: An Update From the COV-AD Study
title_full_unstemmed Increased Seroprevalence and Improved Antibody Responses Following Third Primary SARS-CoV-2 Immunisation: An Update From the COV-AD Study
title_short Increased Seroprevalence and Improved Antibody Responses Following Third Primary SARS-CoV-2 Immunisation: An Update From the COV-AD Study
title_sort increased seroprevalence and improved antibody responses following third primary sars-cov-2 immunisation: an update from the cov-ad study
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9201027/
https://www.ncbi.nlm.nih.gov/pubmed/35720400
http://dx.doi.org/10.3389/fimmu.2022.912571
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