<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>28(5)</volume><submitter>Ram R</submitter><pubmed_abstract>Patients with delayed B-cell reconstitution/B-cell aplasia after cellular therapy show decreased immunogenicity to the BNT162b2 mRNA COVID-19 vaccine. We prospectively evaluated both humoral and cellular immune response to a third vaccine dose in patients after allogeneic HCT (n = 10) or CD19-based chimeric antigen receptor T cells (CAR-T) therapy (n = 6) with low absolute B cell numbers and who failed to mount a humeral response after 2 vaccine doses. Humoral response was documented in 40% and 17% after allogeneic HCT and CAR-T therapy, respectively. None of the patients with complete B-cell aplasia developed anti-vaccine antibodies. Cellular response was documented in all patients after allogeneic HCT and in 83% of the patients after CAR-T. T-cell subclasses levels were not predictive fo</pubmed_abstract><journal>Transplantation and cellular therapy</journal><pagination>278.e1-278.e4</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8848544</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Immunogenicity of a Third Dose of the BNT162b2 mRNA Covid-19 Vaccine in Patients with Impaired B Cell Reconstitution After Cellular Therapy-A Single Center Prospective Cohort Study.</pubmed_title><pmcid>PMC8848544</pmcid><pubmed_authors>Freund T</pubmed_authors><pubmed_authors>Bar-On Y</pubmed_authors><pubmed_authors>Ram R</pubmed_authors><pubmed_authors>Halperin T</pubmed_authors><pubmed_authors>Beyar-Katz O</pubmed_authors><pubmed_authors>Ben-Ami R</pubmed_authors><pubmed_authors>Eilaty N</pubmed_authors><pubmed_authors>Gold R</pubmed_authors><pubmed_authors>Hagin D</pubmed_authors><pubmed_authors>Glait-Santar C</pubmed_authors><pubmed_authors>Kay S</pubmed_authors><pubmed_authors>Amit O</pubmed_authors></additional><is_claimable>false</is_claimable><name>Immunogenicity of a Third Dose of the BNT162b2 mRNA Covid-19 Vaccine in Patients with Impaired B Cell Reconstitution After Cellular Therapy-A Single Center Prospective Cohort Study.</name><description>Patients with delayed B-cell reconstitution/B-cell aplasia after cellular therapy show decreased immunogenicity to the BNT162b2 mRNA COVID-19 vaccine. We prospectively evaluated both humoral and cellular immune response to a third vaccine dose in patients after allogeneic HCT (n = 10) or CD19-based chimeric antigen receptor T cells (CAR-T) therapy (n = 6) with low absolute B cell numbers and who failed to mount a humeral response after 2 vaccine doses. Humoral response was documented in 40% and 17% after allogeneic HCT and CAR-T therapy, respectively. None of the patients with complete B-cell aplasia developed anti-vaccine antibodies. Cellular response was documented in all patients after allogeneic HCT and in 83% of the patients after CAR-T. T-cell subclasses levels were not predictive fo</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 May</publication><modification>2026-05-03T03:16:27.02Z</modification><creation>2024-10-19T13:18:35.471Z</creation></dates><accession>S-EPMC8848544</accession><cross_references><pubmed>35182795</pubmed><doi>10.1016/j.jtct.2022.02.012</doi></cross_references></HashMap>