<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Rakshit S</submitter><funding>NIAID NIH HHS</funding><pagination>985938</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9577398</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13</volume><pubmed_abstract>This proof-of-concept study tested if prior BCG revaccination can qualitatively and quantitively enhance antibody and T-cell responses induced by Oxford/AstraZeneca ChAdOx1nCoV-19 or COVISHIELD™, an efficacious and the most widely distributed vaccine in India. We compared COVISHIELD™ induced longitudinal immune responses in 21 BCG re-vaccinees (BCG-RV) and 13 BCG-non-revaccinees (BCG-NRV), all of whom were BCG vaccinated at birth; latent tuberculosis negative and SARS-CoV-2 seronegative prior to COVISHIELD™ vaccination. Compared to BCG-NRV, BCG-RV displayed significantly higher and persistent spike-specific neutralizing (n) Ab titers and polyfunctional CD4+ and CD8+ T-cells for eight months post COVISHIELD™ booster, including distinct CD4+IFN-γ+ and CD4+IFN-γ- effector memory (EM) subsets </pubmed_abstract><journal>Frontiers in immunology</journal><pubmed_title>Evidence for the heterologous benefits of prior BCG vaccination on COVISHIELD™ vaccine-induced immune responses in SARS-CoV-2 seronegative young Indian adults.</pubmed_title><pmcid>PMC9577398</pmcid><funding_grant_id>UM1 AI068618</funding_grant_id><pubmed_authors>Maguire TJA</pubmed_authors><pubmed_authors>Ottenhoff THM</pubmed_authors><pubmed_authors>Rao S</pubmed_authors><pubmed_authors>Adiga V</pubmed_authors><pubmed_authors>Shivalingaiah S</pubmed_authors><pubmed_authors>Parthiban C</pubmed_authors><pubmed_authors>Rakshit S</pubmed_authors><pubmed_authors>Joosten SA</pubmed_authors><pubmed_authors>Ahmed A</pubmed_authors><pubmed_authors>McElrath MJ</pubmed_authors><pubmed_authors>Netea MG</pubmed_authors><pubmed_authors>Geckin B</pubmed_authors><pubmed_authors>Chetan Kumar N</pubmed_authors><pubmed_authors>Dasgupta P</pubmed_authors><pubmed_authors>Vyakarnam A</pubmed_authors><pubmed_authors>van Meijgaarden KE</pubmed_authors><pubmed_authors>Babji S</pubmed_authors><pubmed_authors>D'Souza G</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Doores KJ</pubmed_authors><pubmed_authors>De Rosa SC</pubmed_authors><pubmed_authors>Dwarkanath P</pubmed_authors><pubmed_authors>Stuart KD</pubmed_authors><pubmed_authors>Dias M</pubmed_authors><pubmed_authors>Zoodsma M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Evidence for the heterologous benefits of prior BCG vaccination on COVISHIELD™ vaccine-induced immune responses in SARS-CoV-2 seronegative young Indian adults.</name><description>This proof-of-concept study tested if prior BCG revaccination can qualitatively and quantitively enhance antibody and T-cell responses induced by Oxford/AstraZeneca ChAdOx1nCoV-19 or COVISHIELD™, an efficacious and the most widely distributed vaccine in India. We compared COVISHIELD™ induced longitudinal immune responses in 21 BCG re-vaccinees (BCG-RV) and 13 BCG-non-revaccinees (BCG-NRV), all of whom were BCG vaccinated at birth; latent tuberculosis negative and SARS-CoV-2 seronegative prior to COVISHIELD™ vaccination. Compared to BCG-NRV, BCG-RV displayed significantly higher and persistent spike-specific neutralizing (n) Ab titers and polyfunctional CD4+ and CD8+ T-cells for eight months post COVISHIELD™ booster, including distinct CD4+IFN-γ+ and CD4+IFN-γ- effector memory (EM) subsets </description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2026-05-08T03:10:24.496Z</modification><creation>2025-02-19T03:23:00.591Z</creation></dates><accession>S-EPMC9577398</accession><cross_references><pubmed>36268023</pubmed><doi>10.3389/fimmu.2022.985938</doi></cross_references></HashMap>