<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Hod T</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>The effectiveness of the fourth BNT162b2 vaccination in reducing the rate and severity of coronavirus disease 2019 (COVID-19) caused by the Omicron variant in renal transplant recipients (RTRs) is unknown.&lt;h4>Methods&lt;/h4>Interviews were conducted with 447 RTRs regarding the status and timing of the fourth vaccination, prior vaccinations, and preceding COVID-19 infection. RTRs with polymerase chain reaction-confirmed COVID-19 infection from December 1, 2021, to the end of March 2022 were considered to have been infected with the Omicron variant and were interviewed to determine their disease severity. In a subgroup of 74 RTRs, the humoral response to the fourth dose was analyzed. In 30 RTRs, microneutralization assays were performed to reveal the humoral response to wild-type, Delta, and Omicron variant isolates before and after the fourth dose.&lt;h4>Results&lt;/h4>Of 447 RTRs, 144 (32.2%) were infected with the Omicron variant, with 71 (49.3%) of the infected RTRs having received the fourth vaccine dose. RTRs who did not receive the fourth dose before the infection had more serious illness. In a subgroup of 74 RTRs, the fourth dose elicited a positive humoral response in 94.6% (70/74), with a significant increase in geometric mean titer for receptor-binding domain immunoglobulin G and neutralizing antibodies (P &lt; 0.001). The humoral responses to the Omicron variant before and after the fourth dose were significantly lower than the responses to the wild-type and the Delta variants.&lt;h4>Conclusion&lt;/h4>Overall, the fourth BNT162b2 dose was effective in reducing the rate and severity of Omicron disease in RTRs, despite the reduced humoral response to the variant.</pubmed_abstract><journal>Transplantation</journal><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9746231</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Humoral Response to the Fourth BNT162b2 Vaccination and Link Between the Fourth Dose, Omicron Infection, and Disease Severity in Renal Transplant Recipients.</pubmed_title><pmcid>PMC9746231</pmcid><pubmed_authors>Atari N</pubmed_authors><pubmed_authors>Halperin R</pubmed_authors><pubmed_authors>Lustig Y</pubmed_authors><pubmed_authors>Benjamini O</pubmed_authors><pubmed_authors>Mor E</pubmed_authors><pubmed_authors>Grossman E</pubmed_authors><pubmed_authors>Olmer L</pubmed_authors><pubmed_authors>Mandelboim M</pubmed_authors><pubmed_authors>Asraf K</pubmed_authors><pubmed_authors>Indenbaum V</pubmed_authors><pubmed_authors>Doolman R</pubmed_authors><pubmed_authors>Ben-David A</pubmed_authors><pubmed_authors>Rahav G</pubmed_authors><pubmed_authors>Hod T</pubmed_authors><pubmed_authors>Beckerman P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Humoral Response to the Fourth BNT162b2 Vaccination and Link Between the Fourth Dose, Omicron Infection, and Disease Severity in Renal Transplant Recipients.</name><description>&lt;h4>Background&lt;/h4>The effectiveness of the fourth BNT162b2 vaccination in reducing the rate and severity of coronavirus disease 2019 (COVID-19) caused by the Omicron variant in renal transplant recipients (RTRs) is unknown.&lt;h4>Methods&lt;/h4>Interviews were conducted with 447 RTRs regarding the status and timing of the fourth vaccination, prior vaccinations, and preceding COVID-19 infection. RTRs with polymerase chain reaction-confirmed COVID-19 infection from December 1, 2021, to the end of March 2022 were considered to have been infected with the Omicron variant and were interviewed to determine their disease severity. In a subgroup of 74 RTRs, the humoral response to the fourth dose was analyzed. In 30 RTRs, microneutralization assays were performed to reveal the humoral response to wild-type, Delta, and Omicron variant isolates before and after the fourth dose.&lt;h4>Results&lt;/h4>Of 447 RTRs, 144 (32.2%) were infected with the Omicron variant, with 71 (49.3%) of the infected RTRs having received the fourth vaccine dose. RTRs who did not receive the fourth dose before the infection had more serious illness. In a subgroup of 74 RTRs, the fourth dose elicited a positive humoral response in 94.6% (70/74), with a significant increase in geometric mean titer for receptor-binding domain immunoglobulin G and neutralizing antibodies (P &lt; 0.001). The humoral responses to the Omicron variant before and after the fourth dose were significantly lower than the responses to the wild-type and the Delta variants.&lt;h4>Conclusion&lt;/h4>Overall, the fourth BNT162b2 dose was effective in reducing the rate and severity of Omicron disease in RTRs, despite the reduced humoral response to the variant.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Oct</publication><modification>2025-04-04T19:11:19.251Z</modification><creation>2025-02-19T00:47:19.833Z</creation></dates><accession>S-EPMC9746231</accession><cross_references><pubmed>36367927</pubmed><doi>10.1097/TP.0000000000004383</doi></cross_references></HashMap>