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Three-Month Follow-Up of Heterologous vs. Homologous Third SARS-CoV-2 Vaccination in Kidney Transplant Recipients: Secondary Analysis of a Randomized Controlled Trial

Response to SARS-CoV-2-vaccines in kidney-transplant recipients (KTR) is severely reduced. Heterologous3(rd) vaccination combining mRNA and vector vaccines did not increase seroconversion at 4 weeks after vaccination, but evolution of antibody levels beyond the first month remains unknown. We have r...

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Autores principales: Heinzel, Andreas, Schrezenmeier, Eva, Regele, Florina, Hu, Karin, Raab, Lukas, Eder, Michael, Aigner, Christof, Jabbour, Rhea, Aschauer, Constantin, Stefanski, Ana-Luisa, Dörner, Thomas, Budde, Klemens, Reindl-Schwaighofer, Roman, Oberbauer, Rainer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9353321/
https://www.ncbi.nlm.nih.gov/pubmed/35935786
http://dx.doi.org/10.3389/fmed.2022.936126
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author Heinzel, Andreas
Schrezenmeier, Eva
Regele, Florina
Hu, Karin
Raab, Lukas
Eder, Michael
Aigner, Christof
Jabbour, Rhea
Aschauer, Constantin
Stefanski, Ana-Luisa
Dörner, Thomas
Budde, Klemens
Reindl-Schwaighofer, Roman
Oberbauer, Rainer
author_facet Heinzel, Andreas
Schrezenmeier, Eva
Regele, Florina
Hu, Karin
Raab, Lukas
Eder, Michael
Aigner, Christof
Jabbour, Rhea
Aschauer, Constantin
Stefanski, Ana-Luisa
Dörner, Thomas
Budde, Klemens
Reindl-Schwaighofer, Roman
Oberbauer, Rainer
author_sort Heinzel, Andreas
collection PubMed
description Response to SARS-CoV-2-vaccines in kidney-transplant recipients (KTR) is severely reduced. Heterologous3(rd) vaccination combining mRNA and vector vaccines did not increase seroconversion at 4 weeks after vaccination, but evolution of antibody levels beyond the first month remains unknown. We have recently completed a randomized-controlled trial on heterologous (Ad26COVS1) vs. homologous (BNT162b2 or mRNA-1273) 3(rd) vaccination in 201 KTR not developing SARS-CoV-2-spike-protein antibodies following two doses of mRNA vaccine (EurdraCT: 2021-002927-39). Here, we report seroconversion at the second follow-up at 3 months after the 3(rd) vaccination (prespecified secondary endpoint). In addition, higher cut-off levels associated with neutralizing capacity and protective immunity were applied (i.e., > 15, > 100, > 141, and > 264 BAU/ml). A total of 169 patients were available for the 3-month follow-up. Overall, seroconversion at 3 months was similar between both groups (45 vs. 50% for mRNA and the vector group, respectively; p = 0.539). However, when applying higher cut-off levels, a significantly larger number of individuals in the vector group reached antibody levels > 141 and > 264 BAU/ml at the 3-month follow-up (141 BAU/ml: 4 vs. 15%, p = 0.009 and 264 BAU/ml: 1 vs. 10%, p = 0.018 for mRNA vs. the vector vaccine group, respectively). In line, antibody levels in seroconverted patients further increased from month 1 to month 3 in the vector group while remaining unchanged in the mRNA group (median increase: mRNA = 1.35 U/ml and vector = 27.6 U/ml, p = 0.004). Despite a similar overall seroconversion rate at 3 months following 3(rd) vaccination in KTR, a heterologous 3rd booster vaccination with Ad26COVS1 resulted in significantly higher antibody levels in responders.
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spelling pubmed-93533212022-08-06 Three-Month Follow-Up of Heterologous vs. Homologous Third SARS-CoV-2 Vaccination in Kidney Transplant Recipients: Secondary Analysis of a Randomized Controlled Trial Heinzel, Andreas Schrezenmeier, Eva Regele, Florina Hu, Karin Raab, Lukas Eder, Michael Aigner, Christof Jabbour, Rhea Aschauer, Constantin Stefanski, Ana-Luisa Dörner, Thomas Budde, Klemens Reindl-Schwaighofer, Roman Oberbauer, Rainer Front Med (Lausanne) Medicine Response to SARS-CoV-2-vaccines in kidney-transplant recipients (KTR) is severely reduced. Heterologous3(rd) vaccination combining mRNA and vector vaccines did not increase seroconversion at 4 weeks after vaccination, but evolution of antibody levels beyond the first month remains unknown. We have recently completed a randomized-controlled trial on heterologous (Ad26COVS1) vs. homologous (BNT162b2 or mRNA-1273) 3(rd) vaccination in 201 KTR not developing SARS-CoV-2-spike-protein antibodies following two doses of mRNA vaccine (EurdraCT: 2021-002927-39). Here, we report seroconversion at the second follow-up at 3 months after the 3(rd) vaccination (prespecified secondary endpoint). In addition, higher cut-off levels associated with neutralizing capacity and protective immunity were applied (i.e., > 15, > 100, > 141, and > 264 BAU/ml). A total of 169 patients were available for the 3-month follow-up. Overall, seroconversion at 3 months was similar between both groups (45 vs. 50% for mRNA and the vector group, respectively; p = 0.539). However, when applying higher cut-off levels, a significantly larger number of individuals in the vector group reached antibody levels > 141 and > 264 BAU/ml at the 3-month follow-up (141 BAU/ml: 4 vs. 15%, p = 0.009 and 264 BAU/ml: 1 vs. 10%, p = 0.018 for mRNA vs. the vector vaccine group, respectively). In line, antibody levels in seroconverted patients further increased from month 1 to month 3 in the vector group while remaining unchanged in the mRNA group (median increase: mRNA = 1.35 U/ml and vector = 27.6 U/ml, p = 0.004). Despite a similar overall seroconversion rate at 3 months following 3(rd) vaccination in KTR, a heterologous 3rd booster vaccination with Ad26COVS1 resulted in significantly higher antibody levels in responders. Frontiers Media S.A. 2022-07-22 /pmc/articles/PMC9353321/ /pubmed/35935786 http://dx.doi.org/10.3389/fmed.2022.936126 Text en Copyright © 2022 Heinzel, Schrezenmeier, Regele, Hu, Raab, Eder, Aigner, Jabbour, Aschauer, Stefanski, Dörner, Budde, Reindl-Schwaighofer and Oberbauer. 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 Medicine
Heinzel, Andreas
Schrezenmeier, Eva
Regele, Florina
Hu, Karin
Raab, Lukas
Eder, Michael
Aigner, Christof
Jabbour, Rhea
Aschauer, Constantin
Stefanski, Ana-Luisa
Dörner, Thomas
Budde, Klemens
Reindl-Schwaighofer, Roman
Oberbauer, Rainer
Three-Month Follow-Up of Heterologous vs. Homologous Third SARS-CoV-2 Vaccination in Kidney Transplant Recipients: Secondary Analysis of a Randomized Controlled Trial
title Three-Month Follow-Up of Heterologous vs. Homologous Third SARS-CoV-2 Vaccination in Kidney Transplant Recipients: Secondary Analysis of a Randomized Controlled Trial
title_full Three-Month Follow-Up of Heterologous vs. Homologous Third SARS-CoV-2 Vaccination in Kidney Transplant Recipients: Secondary Analysis of a Randomized Controlled Trial
title_fullStr Three-Month Follow-Up of Heterologous vs. Homologous Third SARS-CoV-2 Vaccination in Kidney Transplant Recipients: Secondary Analysis of a Randomized Controlled Trial
title_full_unstemmed Three-Month Follow-Up of Heterologous vs. Homologous Third SARS-CoV-2 Vaccination in Kidney Transplant Recipients: Secondary Analysis of a Randomized Controlled Trial
title_short Three-Month Follow-Up of Heterologous vs. Homologous Third SARS-CoV-2 Vaccination in Kidney Transplant Recipients: Secondary Analysis of a Randomized Controlled Trial
title_sort three-month follow-up of heterologous vs. homologous third sars-cov-2 vaccination in kidney transplant recipients: secondary analysis of a randomized controlled trial
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9353321/
https://www.ncbi.nlm.nih.gov/pubmed/35935786
http://dx.doi.org/10.3389/fmed.2022.936126
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