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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 re...
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Published in: | Frontiers in medicine 2022-07, Vol.9, p.936126-936126 |
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creator | 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 |
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. |
doi_str_mv | 10.3389/fmed.2022.936126 |
format | article |
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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.</description><identifier>ISSN: 2296-858X</identifier><identifier>EISSN: 2296-858X</identifier><identifier>DOI: 10.3389/fmed.2022.936126</identifier><identifier>PMID: 35935786</identifier><language>eng</language><publisher>Frontiers Media S.A</publisher><subject>COVID-19 ; COVID-19 vaccination ; heterologous vaccination ; kidney transplantation ; Medicine ; third vaccination</subject><ispartof>Frontiers in medicine, 2022-07, Vol.9, p.936126-936126</ispartof><rights>Copyright © 2022 Heinzel, Schretzenmeier, Regele, Hu, Raab, Eder, Aigner, Jabbour, Aschauer, Stefanski, Dörner, Budde, Reindl-Schwaighofer and Oberbauer. 2022 Heinzel, Schretzenmeier, Regele, Hu, Raab, Eder, Aigner, Jabbour, Aschauer, Stefanski, Dörner, Budde, Reindl-Schwaighofer and Oberbauer</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c439t-e1e0388c1abca5581acd2dc6433d1186a7a4be646f10a8c96df634668afac3af3</citedby><cites>FETCH-LOGICAL-c439t-e1e0388c1abca5581acd2dc6433d1186a7a4be646f10a8c96df634668afac3af3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9353321/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9353321/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids></links><search><creatorcontrib>Heinzel, Andreas</creatorcontrib><creatorcontrib>Schrezenmeier, Eva</creatorcontrib><creatorcontrib>Regele, Florina</creatorcontrib><creatorcontrib>Hu, Karin</creatorcontrib><creatorcontrib>Raab, Lukas</creatorcontrib><creatorcontrib>Eder, Michael</creatorcontrib><creatorcontrib>Aigner, Christof</creatorcontrib><creatorcontrib>Jabbour, Rhea</creatorcontrib><creatorcontrib>Aschauer, Constantin</creatorcontrib><creatorcontrib>Stefanski, Ana-Luisa</creatorcontrib><creatorcontrib>Dörner, Thomas</creatorcontrib><creatorcontrib>Budde, Klemens</creatorcontrib><creatorcontrib>Reindl-Schwaighofer, Roman</creatorcontrib><creatorcontrib>Oberbauer, Rainer</creatorcontrib><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><title>Frontiers in medicine</title><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.</description><subject>COVID-19</subject><subject>COVID-19 vaccination</subject><subject>heterologous vaccination</subject><subject>kidney transplantation</subject><subject>Medicine</subject><subject>third vaccination</subject><issn>2296-858X</issn><issn>2296-858X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpVkktvEzEUhUcIRKvSPUsv2UzwY8axWSBFEW0qipCStGJn3fiRuHLsYE-Kwg_id-KQgujK1_bVd659TtO8JXjEmJDv3daaEcWUjiTjhPIXzTmlkreiF99e_lefNZelPGCMCaN9R9jr5oz1kvVjwc-bX8tNtrb9kuKwQVcphPSjvduh5NDMDjankNZpX9BjGaFZ2v7dLjc-G7SYzBftNN23FN2D1j7C4FNEPqLP3kR7QMsMsewCxAHNrfY7b-NQPqCF1SkayAc0iRAOxZejHqA5RJO2_qc1aFrnqeKhlsvsIbxpXjkIxV4-rRfN3dWn5XTW3n69vplOblvdMTm0lljMhNAEVhr6XhDQhhrNO8YMIYLDGLqV5R13BIPQkhvHWce5AAeagWMXzc2JaxI8qF322zqmSuDVn4OU1wry4HWwyhIjnesdxYJ3vXVyRaCX0hrnMHRjW1kfT6zdflWt0vXxGcIz6POb6DdqnR5V9YYxSirg3RMgp-97Wwa19UXbUD_UVhcU5VLKXggsais-teqcSsnW_ZMhWB3Too5pUce0qFNa2G_D8LYW</recordid><startdate>20220722</startdate><enddate>20220722</enddate><creator>Heinzel, Andreas</creator><creator>Schrezenmeier, Eva</creator><creator>Regele, Florina</creator><creator>Hu, Karin</creator><creator>Raab, Lukas</creator><creator>Eder, Michael</creator><creator>Aigner, Christof</creator><creator>Jabbour, Rhea</creator><creator>Aschauer, Constantin</creator><creator>Stefanski, Ana-Luisa</creator><creator>Dörner, Thomas</creator><creator>Budde, Klemens</creator><creator>Reindl-Schwaighofer, Roman</creator><creator>Oberbauer, Rainer</creator><general>Frontiers Media S.A</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20220722</creationdate><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><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></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c439t-e1e0388c1abca5581acd2dc6433d1186a7a4be646f10a8c96df634668afac3af3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>COVID-19</topic><topic>COVID-19 vaccination</topic><topic>heterologous vaccination</topic><topic>kidney transplantation</topic><topic>Medicine</topic><topic>third vaccination</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Heinzel, Andreas</creatorcontrib><creatorcontrib>Schrezenmeier, Eva</creatorcontrib><creatorcontrib>Regele, Florina</creatorcontrib><creatorcontrib>Hu, Karin</creatorcontrib><creatorcontrib>Raab, Lukas</creatorcontrib><creatorcontrib>Eder, Michael</creatorcontrib><creatorcontrib>Aigner, Christof</creatorcontrib><creatorcontrib>Jabbour, Rhea</creatorcontrib><creatorcontrib>Aschauer, Constantin</creatorcontrib><creatorcontrib>Stefanski, Ana-Luisa</creatorcontrib><creatorcontrib>Dörner, Thomas</creatorcontrib><creatorcontrib>Budde, Klemens</creatorcontrib><creatorcontrib>Reindl-Schwaighofer, Roman</creatorcontrib><creatorcontrib>Oberbauer, Rainer</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Frontiers in medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Heinzel, Andreas</au><au>Schrezenmeier, Eva</au><au>Regele, Florina</au><au>Hu, Karin</au><au>Raab, Lukas</au><au>Eder, Michael</au><au>Aigner, Christof</au><au>Jabbour, Rhea</au><au>Aschauer, Constantin</au><au>Stefanski, Ana-Luisa</au><au>Dörner, Thomas</au><au>Budde, Klemens</au><au>Reindl-Schwaighofer, Roman</au><au>Oberbauer, Rainer</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Three-Month Follow-Up of Heterologous vs. Homologous Third SARS-CoV-2 Vaccination in Kidney Transplant Recipients: Secondary Analysis of a Randomized Controlled Trial</atitle><jtitle>Frontiers in medicine</jtitle><date>2022-07-22</date><risdate>2022</risdate><volume>9</volume><spage>936126</spage><epage>936126</epage><pages>936126-936126</pages><issn>2296-858X</issn><eissn>2296-858X</eissn><abstract>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.</abstract><pub>Frontiers Media S.A</pub><pmid>35935786</pmid><doi>10.3389/fmed.2022.936126</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | COVID-19 COVID-19 vaccination heterologous vaccination kidney transplantation Medicine third vaccination |
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 |
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