Temporal profiling of human lymphoid tissues reveals coordinated defence to viral challenge

Coates, M. L.; Richoz, N.; Tuong, Z. K.; Bowyer, G.; Lee, C. Y. C.; Ferdinand, J. R.; Gillman, E.; McClure, M.; Di Marco Barros, R.; Stewart, B. J.; Clatworthy, M. R.

doi:10.1101/2023.09.15.558006

bioRxiv · 10.1101/2023.09.15.558006

Temporal profiling of human lymphoid tissues reveals coordinated defence to viral challenge

Coates, M. L.·Richoz, N.·Tuong, Z. K.·Bowyer, G.·Lee, C. Y. C.·Ferdinand, J. R.·Gillman, E.·McClure, M.·Di Marco Barros, R.·Stewart, B. J.·Clatworthy, M. R.

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Abstract

Adaptive immunity is generated in lymphoid organs, but how these structures defend themselves during infection in humans is unknown. The nasal epithelium is a major site of viral entry, with adenoid nasal-associated lymphoid tissue (NALT) generating early adaptive responses. Here, using a nasopharyngeal biopsy, we examined longitudinal immune responses in NALT following viral challenge, using SARS-CoV-2 infection as a natural experimental model. In acute infection, infiltrating monocytes formed a subepithelial and peri-follicular shield, recruiting NET-forming neutrophils, whilst tissue macrophages expressed pro-repair molecules during convalescence to promote the restoration of tissue integrity. Germinal centre B cells expressed anti-viral transcripts that inversely correlated with fate-defining transcription factors. Among T cells, tissue-resident memory CD8 T cells alone showed clonal expansion and maintained cytotoxic transcriptional programmes into convalescence. Together our study provides a unique insight into how human nasal adaptive immune responses are generated and sustained in the face of viral challenge.

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Coates, M. L., Richoz, N., Tuong, Z. K., Bowyer, G., Lee, C. Y. C., Ferdinand, J. R., Gillman, E., McClure, M., Di Marco Barros, R., Stewart, B. J., Clatworthy, M. R.. 2023-09-17. Temporal profiling of human lymphoid tissues reveals coordinated defence to viral challenge. https://doi.org/10.1101/2023.09.15.558006

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