<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>197(3)</volume><submitter>Ujjani C</submitter><funding>Fred Hutchinson Cancer Research Center</funding><funding>Andy Hill CARE Fund</funding><pubmed_abstract>Prior reports evaluating SARS-CoV-2 vaccine efficacy in chronic lymphocytic leukaemia (CLL) used semiquantitative measurements of anti-S to evaluate immunity; however, neutralization assays were used to assess functional immunity in the trials leading to vaccine approval. Here, we identified decreased rates of seroconversion in vaccinated CLL patients and lower anti-S levels compared to healthy controls. Notably, we demonstrated similar results with the Roche anti-S assay and neutralization activity. Durable responses were seen at six months; augmentation with boosters was possible in responding patients. Absence of normal B cells, frequently seen in patients receiving Bruton tyrosine kinase and B-cell lymphoma 2 inhibitors, was a strong predictor of lack of seroconversion.</pubmed_abstract><journal>British journal of haematology</journal><pagination>306-309</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9111753</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The impact of B-cell-directed therapy on SARS-CoV-2 vaccine efficacy in chronic lymphocytic leukaemia.</pubmed_title><pmcid>PMC9111753</pmcid><pubmed_authors>Sorensen T</pubmed_authors><pubmed_authors>Lee S</pubmed_authors><pubmed_authors>Huang ML</pubmed_authors><pubmed_authors>Tu B</pubmed_authors><pubmed_authors>Smith SD</pubmed_authors><pubmed_authors>Hill JA</pubmed_authors><pubmed_authors>Lynch RC</pubmed_authors><pubmed_authors>Zhu H</pubmed_authors><pubmed_authors>Till BG</pubmed_authors><pubmed_authors>Ujjani C</pubmed_authors><pubmed_authors>Stevenson PA</pubmed_authors><pubmed_authors>Grainger C</pubmed_authors><pubmed_authors>Warren EH</pubmed_authors><pubmed_authors>Shadman M</pubmed_authors><pubmed_authors>Gausman D</pubmed_authors><pubmed_authors>Poh C</pubmed_authors><pubmed_authors>Gopal AK</pubmed_authors><pubmed_authors>Nielsen L</pubmed_authors><pubmed_authors>Greninger A</pubmed_authors><pubmed_authors>Gooley T</pubmed_authors></additional><is_claimable>false</is_claimable><name>The impact of B-cell-directed therapy on SARS-CoV-2 vaccine efficacy in chronic lymphocytic leukaemia.</name><description>Prior reports evaluating SARS-CoV-2 vaccine efficacy in chronic lymphocytic leukaemia (CLL) used semiquantitative measurements of anti-S to evaluate immunity; however, neutralization assays were used to assess functional immunity in the trials leading to vaccine approval. Here, we identified decreased rates of seroconversion in vaccinated CLL patients and lower anti-S levels compared to healthy controls. Notably, we demonstrated similar results with the Roche anti-S assay and neutralization activity. Durable responses were seen at six months; augmentation with boosters was possible in responding patients. Absence of normal B cells, frequently seen in patients receiving Bruton tyrosine kinase and B-cell lymphoma 2 inhibitors, was a strong predictor of lack of seroconversion.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 May</publication><modification>2026-05-31T20:59:49.529Z</modification><creation>2025-02-19T04:21:04.195Z</creation></dates><accession>S-EPMC9111753</accession><cross_references><pubmed>35149986</pubmed><doi>10.1111/bjh.18088</doi></cross_references></HashMap>