<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>22(1)</volume><submitter>Aiello A</submitter><pubmed_abstract>Aging is frequently characterized by an inadequate primary vaccine response, likely due to immunosenescence and inflamm-aging, a low-level, chronic inflammatory state. Both aspects increase the susceptibility of older adults to viral and bacterial infections, resulting in a higher frequency and severity of infectious diseases. In this preliminary study, a cohort of 52 individuals was recruited and divided into two groups: young (age range 21-35) and older adults (> 60 years old). Peripheral blood mononuclear cells (PBMCs) were collected before (time 0, T0) and after (time 1, T1) the immunization with a tetravalent influenza vaccine. Then, T cell immunophenotyping analysis was conducted to investigate how aging and influenza vaccination influence T cell responses. Additionally, the anti-inf</pubmed_abstract><journal>Immunity &amp; ageing : I &amp; A</journal><pagination>13</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11938677</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Enhancing flu vaccine responses in older adults: preliminary insights from the ISOLDA study on immunosenescence and antioxidant and anti-inflammatory approaches.</pubmed_title><pmcid>PMC11938677</pmcid><pubmed_authors>Manna MP</pubmed_authors><pubmed_authors>Calabro A</pubmed_authors><pubmed_authors>Azgomi MS</pubmed_authors><pubmed_authors>Procopio A</pubmed_authors><pubmed_authors>Ligotti ME</pubmed_authors><pubmed_authors>Dieli F</pubmed_authors><pubmed_authors>Accardi G</pubmed_authors><pubmed_authors>Caruso C</pubmed_authors><pubmed_authors>Aiello A</pubmed_authors><pubmed_authors>Candore G</pubmed_authors><pubmed_authors>Caccamo N</pubmed_authors></additional><is_claimable>false</is_claimable><name>Enhancing flu vaccine responses in older adults: preliminary insights from the ISOLDA study on immunosenescence and antioxidant and anti-inflammatory approaches.</name><description>Aging is frequently characterized by an inadequate primary vaccine response, likely due to immunosenescence and inflamm-aging, a low-level, chronic inflammatory state. Both aspects increase the susceptibility of older adults to viral and bacterial infections, resulting in a higher frequency and severity of infectious diseases. In this preliminary study, a cohort of 52 individuals was recruited and divided into two groups: young (age range 21-35) and older adults (> 60 years old). Peripheral blood mononuclear cells (PBMCs) were collected before (time 0, T0) and after (time 1, T1) the immunization with a tetravalent influenza vaccine. Then, T cell immunophenotyping analysis was conducted to investigate how aging and influenza vaccination influence T cell responses. Additionally, the anti-inf</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Mar</publication><modification>2025-07-13T03:04:34.318Z</modification><creation>2025-07-13T03:04:34.318Z</creation></dates><accession>S-EPMC11938677</accession><cross_references><pubmed>40140897</pubmed><doi>10.1186/s12979-025-00506-y</doi></cross_references></HashMap>