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

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

PMC · DOI: 10.1126/sciadv.ady8316 · 2026-01-07

## TL;DR

CXCR5+ CD8+ T cells in tonsils have stem-like features and are especially good at targeting EBV, a common virus.

## Contribution

Identifies a CXCR5+ tissue-resident memory CD8+ T cell subset in tonsils with EBV-specific immune surveillance potential.

## Key findings

- Tonsils have the highest frequency of CXCR5+ CD8+ T cells compared to other tissues.
- CXCR5+ CD8+ T cells in tonsils show a PD-1+ resident stem-like phenotype and target EBV latent antigens.
- CXCR5 expression is more common in tonsil CD8+ T cells than in circulating cells, regardless of clonal identity.

## Abstract

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.

CXCR5+ memory CD8+ T cells in tonsils show stem-like resident traits and enrich for latent EBV antigen specificity.

## Linked entities

- **Proteins:** CXCR5 (C-X-C motif chemokine receptor 5), PDCD1 (programmed cell death 1)

## Full-text entities

- **Genes:** GZMK (granzyme K) [NCBI Gene 3003] {aka GrK, TRYP2}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, CXCR5 (C-X-C motif chemokine receptor 5) [NCBI Gene 643] {aka BLR1, CD185, MDR15}, PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}
- **Diseases:** chronic (MESH:D002908), infection (MESH:D007239)
- **Species:** Homo sapiens (human, species) [taxon 9606], human gammaherpesvirus 4 (Epstein Barr virus, no rank) [taxon 10376]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12778062/full.md

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Source: https://tomesphere.com/paper/PMC12778062