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A third dose of SARS-CoV-2 vaccine increases neutralizing antibodies against variants of concern in solid organ transplant recipients

Vaccine-induced SARS-CoV-2 antibody responses are attenuated in solid organ transplant recipients (SOTRs) and breakthrough infections are more common. Additional SARS-CoV-2 vaccine doses increase anti-spike IgG in some SOTRs, but it is uncertain whether neutralization of variants of concern (VOCs) i...

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Autores principales: Karaba, Andrew H., Zhu, Xianming, Liang, Tao, Wang, Kristy H., Rittenhouse, Alex G., Akinde, Olivia, Eby, Yolanda, Ruff, Jessica E., Blankson, Joel N., Abedon, Aura T., Alejo, Jennifer L., Cox, Andrea L., Bailey, Justin R., Thompson, Elizabeth A., Klein, Sabra L., Warren, Daniel S., Garonzik-Wang, Jacqueline M., Boyarsky, Brian J., Sitaras, Ioannis, Pekosz, Andrew, Segev, Dorry L., Tobian, Aaron A.R., Werbel, William A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Transplantation & American Society of Transplant Surgeons. Published by Elsevier Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8983554/
https://www.ncbi.nlm.nih.gov/pubmed/34951746
http://dx.doi.org/10.1111/ajt.16933
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author Karaba, Andrew H.
Zhu, Xianming
Liang, Tao
Wang, Kristy H.
Rittenhouse, Alex G.
Akinde, Olivia
Eby, Yolanda
Ruff, Jessica E.
Blankson, Joel N.
Abedon, Aura T.
Alejo, Jennifer L.
Cox, Andrea L.
Bailey, Justin R.
Thompson, Elizabeth A.
Klein, Sabra L.
Warren, Daniel S.
Garonzik-Wang, Jacqueline M.
Boyarsky, Brian J.
Sitaras, Ioannis
Pekosz, Andrew
Segev, Dorry L.
Tobian, Aaron A.R.
Werbel, William A.
author_facet Karaba, Andrew H.
Zhu, Xianming
Liang, Tao
Wang, Kristy H.
Rittenhouse, Alex G.
Akinde, Olivia
Eby, Yolanda
Ruff, Jessica E.
Blankson, Joel N.
Abedon, Aura T.
Alejo, Jennifer L.
Cox, Andrea L.
Bailey, Justin R.
Thompson, Elizabeth A.
Klein, Sabra L.
Warren, Daniel S.
Garonzik-Wang, Jacqueline M.
Boyarsky, Brian J.
Sitaras, Ioannis
Pekosz, Andrew
Segev, Dorry L.
Tobian, Aaron A.R.
Werbel, William A.
author_sort Karaba, Andrew H.
collection PubMed
description Vaccine-induced SARS-CoV-2 antibody responses are attenuated in solid organ transplant recipients (SOTRs) and breakthrough infections are more common. Additional SARS-CoV-2 vaccine doses increase anti-spike IgG in some SOTRs, but it is uncertain whether neutralization of variants of concern (VOCs) is enhanced. We tested 47 SOTRs for clinical and research anti-spike IgG, pseudoneutralization (ACE2 blocking), and live-virus neutralization (nAb) against VOCs before and after a third SARS-CoV-2 vaccine dose (70% mRNA, 30% Ad26.COV2.S) with comparison to 15 healthy controls after two mRNA vaccine doses. We used correlation analysis to compare anti-spike IgG assays and focused on thresholds associated with neutralization. A third SARS-CoV-2 vaccine dose increased median total anti-spike (1.6-fold), pseudoneutralization against VOCs (2.5-fold vs. Delta), and neutralizing antibodies (1.4-fold against Delta). However, neutralization activity was significantly lower than healthy controls (p < .001); 32% of SOTRs had zero detectable nAb against Delta after third vaccination compared to 100% for controls. Correlation with nAb was seen at anti-spike IgG >4 Log(10)(AU/ml) on the Euroimmun ELISA and >4 Log(10)(AU/ml) on the MSD research assay. These findings highlight benefits of a third vaccine dose for some SOTRs and the need for alternative strategies to improve protection in a significant subset of this population.
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spelling pubmed-89835542023-02-08 A third dose of SARS-CoV-2 vaccine increases neutralizing antibodies against variants of concern in solid organ transplant recipients Karaba, Andrew H. Zhu, Xianming Liang, Tao Wang, Kristy H. Rittenhouse, Alex G. Akinde, Olivia Eby, Yolanda Ruff, Jessica E. Blankson, Joel N. Abedon, Aura T. Alejo, Jennifer L. Cox, Andrea L. Bailey, Justin R. Thompson, Elizabeth A. Klein, Sabra L. Warren, Daniel S. Garonzik-Wang, Jacqueline M. Boyarsky, Brian J. Sitaras, Ioannis Pekosz, Andrew Segev, Dorry L. Tobian, Aaron A.R. Werbel, William A. Am J Transplant Brief Communication Vaccine-induced SARS-CoV-2 antibody responses are attenuated in solid organ transplant recipients (SOTRs) and breakthrough infections are more common. Additional SARS-CoV-2 vaccine doses increase anti-spike IgG in some SOTRs, but it is uncertain whether neutralization of variants of concern (VOCs) is enhanced. We tested 47 SOTRs for clinical and research anti-spike IgG, pseudoneutralization (ACE2 blocking), and live-virus neutralization (nAb) against VOCs before and after a third SARS-CoV-2 vaccine dose (70% mRNA, 30% Ad26.COV2.S) with comparison to 15 healthy controls after two mRNA vaccine doses. We used correlation analysis to compare anti-spike IgG assays and focused on thresholds associated with neutralization. A third SARS-CoV-2 vaccine dose increased median total anti-spike (1.6-fold), pseudoneutralization against VOCs (2.5-fold vs. Delta), and neutralizing antibodies (1.4-fold against Delta). However, neutralization activity was significantly lower than healthy controls (p < .001); 32% of SOTRs had zero detectable nAb against Delta after third vaccination compared to 100% for controls. Correlation with nAb was seen at anti-spike IgG >4 Log(10)(AU/ml) on the Euroimmun ELISA and >4 Log(10)(AU/ml) on the MSD research assay. These findings highlight benefits of a third vaccine dose for some SOTRs and the need for alternative strategies to improve protection in a significant subset of this population. American Society of Transplantation & American Society of Transplant Surgeons. Published by Elsevier Inc. 2022-04 2022-12-30 /pmc/articles/PMC8983554/ /pubmed/34951746 http://dx.doi.org/10.1111/ajt.16933 Text en Copyright © 2022 American Society of Transplantation & American Society of Transplant Surgeons. Published by Elsevier Inc. All rights reserved. Published by Elsevier B.V. All rights reserved. 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 Brief Communication
Karaba, Andrew H.
Zhu, Xianming
Liang, Tao
Wang, Kristy H.
Rittenhouse, Alex G.
Akinde, Olivia
Eby, Yolanda
Ruff, Jessica E.
Blankson, Joel N.
Abedon, Aura T.
Alejo, Jennifer L.
Cox, Andrea L.
Bailey, Justin R.
Thompson, Elizabeth A.
Klein, Sabra L.
Warren, Daniel S.
Garonzik-Wang, Jacqueline M.
Boyarsky, Brian J.
Sitaras, Ioannis
Pekosz, Andrew
Segev, Dorry L.
Tobian, Aaron A.R.
Werbel, William A.
A third dose of SARS-CoV-2 vaccine increases neutralizing antibodies against variants of concern in solid organ transplant recipients
title A third dose of SARS-CoV-2 vaccine increases neutralizing antibodies against variants of concern in solid organ transplant recipients
title_full A third dose of SARS-CoV-2 vaccine increases neutralizing antibodies against variants of concern in solid organ transplant recipients
title_fullStr A third dose of SARS-CoV-2 vaccine increases neutralizing antibodies against variants of concern in solid organ transplant recipients
title_full_unstemmed A third dose of SARS-CoV-2 vaccine increases neutralizing antibodies against variants of concern in solid organ transplant recipients
title_short A third dose of SARS-CoV-2 vaccine increases neutralizing antibodies against variants of concern in solid organ transplant recipients
title_sort third dose of sars-cov-2 vaccine increases neutralizing antibodies against variants of concern in solid organ transplant recipients
topic Brief Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8983554/
https://www.ncbi.nlm.nih.gov/pubmed/34951746
http://dx.doi.org/10.1111/ajt.16933
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