<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Albe JR</submitter><funding>NIAID NIH HHS</funding><pubmed_abstract>Enhancing regulatory T cell (Treg) function offers a compelling therapeutic strategy for autoimmune disease. Engineered IL-2 muteins selectively expand functional Tregs with minimal impact on other immune cells, but their potential to compromise antiviral immunity remains largely unexplored. Here, we used a murine model of Influenza A virus (Flu) infection to determine how IL-2 mutein shapes T cell responses to respiratory virus infection. IL-2 mutein administration prior to infection suppressed Flu-specific (Flu-sp) CD8 T cell responses and altered their localization and phenotype within the lungs, without affecting bystander CD8 T cells. This suppression correlated with reduced antigen presentation molecule expression on conventional dendritic cells (cDCs) early after infection but did n</pubmed_abstract><journal>bioRxiv : the preprint server for biology</journal><pagination>2025.06.10.658962</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12458323</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Divergent effects of a Treg-selective IL-2 mutein on Influenza specific T cell responses.</pubmed_title><pmcid>PMC12458323</pmcid><funding_grant_id>R01 AI154773</funding_grant_id><funding_grant_id>R21 AI172140</funding_grant_id><pubmed_authors>Ziegler SF</pubmed_authors><pubmed_authors>Weinstein KN</pubmed_authors><pubmed_authors>Sarkar S</pubmed_authors><pubmed_authors>Chaudhary A</pubmed_authors><pubmed_authors>Campbell DJ</pubmed_authors><pubmed_authors>Kalia V</pubmed_authors><pubmed_authors>Albe JR</pubmed_authors><pubmed_authors>Khanna A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Divergent effects of a Treg-selective IL-2 mutein on Influenza specific T cell responses.</name><description>Enhancing regulatory T cell (Treg) function offers a compelling therapeutic strategy for autoimmune disease. Engineered IL-2 muteins selectively expand functional Tregs with minimal impact on other immune cells, but their potential to compromise antiviral immunity remains largely unexplored. Here, we used a murine model of Influenza A virus (Flu) infection to determine how IL-2 mutein shapes T cell responses to respiratory virus infection. IL-2 mutein administration prior to infection suppressed Flu-specific (Flu-sp) CD8 T cell responses and altered their localization and phenotype within the lungs, without affecting bystander CD8 T cells. This suppression correlated with reduced antigen presentation molecule expression on conventional dendritic cells (cDCs) early after infection but did n</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-05-31T03:12:22.114Z</modification><creation>2026-05-31T03:07:50.808Z</creation></dates><accession>S-EPMC12458323</accession><cross_references><pubmed>41000731</pubmed><doi>10.1101/2025.06.10.658962</doi></cross_references></HashMap>