<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Karaba AH</submitter><funding>National Institute of Allergy and Infectious Diseases</funding><funding>National Institute of Diabetes and Digestive and Kidney Diseases</funding><funding>NIDDK NIH HHS</funding><funding>NIAID NIH HHS</funding><funding>National Cancer Institute</funding><funding>NCI NIH HHS</funding><funding>NIGMS NIH HHS</funding><pagination>1253-1260</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8983554</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>22(4)</volume><pubmed_abstract>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 &lt; .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&lt;sub>10&lt;/sub> (AU/ml) on the Euroimmun ELISA and >4 Log&lt;sub>10&lt;/sub> (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.</pubmed_abstract><journal>American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons</journal><pubmed_title>A third dose of SARS-CoV-2 vaccine increases neutralizing antibodies against variants of concern in solid organ transplant recipients.</pubmed_title><pmcid>PMC8983554</pmcid><funding_grant_id>K23 AI157893</funding_grant_id><funding_grant_id>HHSN272201400007C</funding_grant_id><funding_grant_id>U01 AI138897</funding_grant_id><funding_grant_id>R01AI120938S1</funding_grant_id><funding_grant_id>K23AI157893</funding_grant_id><funding_grant_id>F32 DK124941</funding_grant_id><funding_grant_id>T32DK007713</funding_grant_id><funding_grant_id>R01 AI120938</funding_grant_id><funding_grant_id>K08AI156021</funding_grant_id><funding_grant_id>T32 GM136577</funding_grant_id><funding_grant_id>F32DK124941</funding_grant_id><funding_grant_id>K08 AI156021</funding_grant_id><funding_grant_id>K23 DK115908</funding_grant_id><funding_grant_id>K24 AI144954</funding_grant_id><funding_grant_id>U54 CA260492</funding_grant_id><funding_grant_id>K24AI144954</funding_grant_id><funding_grant_id>K23DK115908</funding_grant_id><funding_grant_id>U54CA260491</funding_grant_id><funding_grant_id>T32 DK007713</funding_grant_id><pubmed_authors>Liang T</pubmed_authors><pubmed_authors>Blankson JN</pubmed_authors><pubmed_authors>Bailey JR</pubmed_authors><pubmed_authors>Rittenhouse AG</pubmed_authors><pubmed_authors>Abedon AT</pubmed_authors><pubmed_authors>Ruff JE</pubmed_authors><pubmed_authors>Tobian AAR</pubmed_authors><pubmed_authors>Alejo JL</pubmed_authors><pubmed_authors>Akinde O</pubmed_authors><pubmed_authors>Eby Y</pubmed_authors><pubmed_authors>Sitaras I</pubmed_authors><pubmed_authors>Boyarsky BJ</pubmed_authors><pubmed_authors>Garonzik-Wang JM</pubmed_authors><pubmed_authors>Cox AL</pubmed_authors><pubmed_authors>Warren DS</pubmed_authors><pubmed_authors>Zhu X</pubmed_authors><pubmed_authors>Thompson EA</pubmed_authors><pubmed_authors>Wang KH</pubmed_authors><pubmed_authors>Klein SL</pubmed_authors><pubmed_authors>Pekosz A</pubmed_authors><pubmed_authors>Segev DL</pubmed_authors><pubmed_authors>Karaba AH</pubmed_authors><pubmed_authors>Werbel WA</pubmed_authors></additional><is_claimable>false</is_claimable><name>A third dose of SARS-CoV-2 vaccine increases neutralizing antibodies against variants of concern in solid organ transplant recipients.</name><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 &lt; .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&lt;sub>10&lt;/sub> (AU/ml) on the Euroimmun ELISA and >4 Log&lt;sub>10&lt;/sub> (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.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Apr</publication><modification>2026-06-06T01:12:59.412Z</modification><creation>2025-04-05T18:50:52.546Z</creation></dates><accession>S-EPMC8983554</accession><cross_references><pubmed>34951746</pubmed><doi>10.1111/ajt.16933</doi></cross_references></HashMap>