CXCR5 identifies stem-like resident memory CD8⁺ T cells enriched for latent EBV specificity in tonsils.
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Rivera Ballesteros O, Rieble L, Cai C, Sekine T, Nilsén V, Adamo S, Müller TR, Constantz C, Niessl J, White E, Ko Y, Kammann T, Mouchtaridi E, Gao Y, Mily A, Raineri EJM, Stamper C, Marchalot A, Wild N, Brownlie D, Llewellyn-Lacey S, Tibbitt C, Michaëlsson J, Marquardt N, Mjösberg J, Jorns C, Sandberg JK, Driving J, Price DA, Buggert M
Sci Adv 12 (2) eady8316 [2026-01-09; online 2026-01-07]
CXCR5+ CD8+ 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+ CD8+ T cells across multiple sites throughout the human body, with an emphasis on oropharyngeal lymphoid tissues. Tonsils harbored the highest frequencies of CXCR5+ CD8+ 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+ T cells expressed CXCR5 more commonly in tonsils compared to vascular circulation. CXCR5 expression was particularly prominent among tonsil-localized CD8+ T cells targeting Epstein-Barr virus (EBV) latent antigens and associated with a PD-1+ resident stem-like phenotype. These data identify a CXCR5+ tissue-resident memory CD8+ T cell subset in human tonsils with a potential role in immune surveillance of EBV.
NGI Stockholm (Genomics Production) [Service]
National Genomics Infrastructure [Service]
PubMed 41499499
DOI 10.1126/sciadv.ady8316
Crossref 10.1126/sciadv.ady8316