{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Rivera Ballesteros O"],"funding":["European Research Council"],"pagination":["eady8316"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC12778062"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["12(2)"],"pubmed_abstract":["CXCR5<sup>+</sup> CD8<sup>+</sup> T cells emerged as key mediators of antiviral immunity in the context of chronic infection. However, their functional attributes and tissue distribution remain incompletely defined, especially in relation to antigen specificity. Here, we investigated the anatomical localization and antiviral properties of CXCR5<sup>+</sup> CD8<sup>+</sup> T cells across multiple sites throughout the human body, with an emphasis on oropharyngeal lymphoid tissues. Tonsils harbored the highest frequencies of CXCR5<sup>+</sup> CD8<sup>+</sup> T cells compared to other tissues, many of which expressed Granzyme K and concurrently displayed tissue residency features, as demonstrated by single cell profiling. Irrespective of clonal identity and virus specificity, CD8<sup>+</sup> T"],"journal":["Science advances"],"pubmed_title":["CXCR5 identifies stem-like resident memory CD8⁺ T cells enriched for latent EBV specificity in tonsils."],"pmcid":["PMC12778062"],"funding_grant_id":["101041484"],"pubmed_authors":["Llewellyn-Lacey S","Constantz C","Michaelsson J","Mouchtaridi E","Marchalot A","Raineri EJM","Sandberg JK","Kammann T","Cai C","Sekine T","Buggert M","Nilsen V","White E","Ko Y","Niessl J","Marquardt N","Jorns C","Rieble L","Price DA","Muller TR","Driving J","Adamo S","Rivera Ballesteros O","Mily A","Wild N","Gao Y","Mjosberg J","Tibbitt C","Stamper C","Brownlie D"],"additional_accession":[]},"is_claimable":false,"name":"CXCR5 identifies stem-like resident memory CD8⁺ T cells enriched for latent EBV specificity in tonsils.","description":"CXCR5<sup>+</sup> CD8<sup>+</sup> T cells emerged as key mediators of antiviral immunity in the context of chronic infection. However, their functional attributes and tissue distribution remain incompletely defined, especially in relation to antigen specificity. Here, we investigated the anatomical localization and antiviral properties of CXCR5<sup>+</sup> CD8<sup>+</sup> T cells across multiple sites throughout the human body, with an emphasis on oropharyngeal lymphoid tissues. Tonsils harbored the highest frequencies of CXCR5<sup>+</sup> CD8<sup>+</sup> T cells compared to other tissues, many of which expressed Granzyme K and concurrently displayed tissue residency features, as demonstrated by single cell profiling. Irrespective of clonal identity and virus specificity, CD8<sup>+</sup> T","dates":{"release":"2026-01-01T00:00:00Z","publication":"2026 Jan","modification":"2026-06-09T05:31:39.931Z","creation":"2026-06-09T03:06:48.866Z"},"accession":"S-EPMC12778062","cross_references":{"pubmed":["41499499"],"doi":["10.1126/sciadv.ady8316"]}}