CXCR5 identifies stem-like resident memory CD8⁺ T cells enriched for latent EBV specificity in tonsils

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 cells expressed CXCR5 more commonly in tonsils compared to vascular circulation. CXCR5 expression was particularly prominent among tonsil-localized CD8<sup>+</sup> T cells targeting Epstein-Barr virus (EBV) latent antigens and associated with a PD-1<sup>+</sup> resident stem-like phenotype. These data identify a CXCR5<sup>+</sup> tissue-resident memory CD8<sup>+</sup> T cell subset in human tonsils with a potential role in immune surveillance of EBV.

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Publication Details

Journal
Science Advances
Published
2026-01-07
DOI
https://doi.org/10.1126/sciadv.ady8316
Primary Topic
Chemokine receptors and signaling
Type
article
Field-Weighted Citation Impact
0.00
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article

CXCR5 identifies stem-like resident memory CD8⁺ T cells enriched for latent EBV specificity in tonsils

Nicole Marquardt, Jakob Michaëlsson, Christopher E. Stamper, Eoghann White et al.
Science Advances
Chemokine receptors and signaling
article

CXCR5 identifies stem-like resident memory CD8⁺ T cells enriched for latent EBV specificity in tonsils

Nicole Marquardt, Jakob Michaëlsson, Christopher E. Stamper, Eoghann White, Carl Jorns, Demi Brownlie, Vera Nilsén, Julia Niessl, Sarah Adamo, Yu Gao, Tobias Kammann, Johan K. Sandberg, Takuya Sekine, Christian M. Constantz, Elli Mouchtaridi, Thomas Müller, Mily Akhirunnesa, DL Price, YouBeen Ko, Nicole Wild, Olga Rivera Ballesteros, Marcus Buggert, Jenny Mjösberg, Chris Tibbitt, Anne Marchalot, Sian Llewellyn-Lacey, Elisa J. M. Raineri, Curtis Cai, Jenny Driving, Lisa Rieble
article en

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 cells expressed CXCR5 more commonly in tonsils compared to vascular circulation. CXCR5 expression was particularly prominent among tonsil-localized CD8<sup>+</sup> T cells targeting Epstein-Barr virus (EBV) latent antigens and associated with a PD-1<sup>+</sup> resident stem-like phenotype. These data identify a CXCR5<sup>+</sup> tissue-resident memory CD8<sup>+</sup> T cell subset in human tonsils with a potential role in immune surveillance of EBV.

Science AdvancesVol. 12(2)
Statistics Sweden (SE), Karolinska University Hospital (SE), Sun Yat-sen University (CN), University Hospital of Wales (GB), University Hospital of Basel (CH), Karolinska Institutet (SE), The First Affiliated Hospital, Sun Yat-sen University (CN), Cardiff University (GB)
Openalex Percentile: Top 96%
Chemokine receptors and signaling
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