bioRxiv · 10.64898/2026.05.05.722858
High-resolution single-cell atlas of the human B cell compartment and immune microenvironment across tissues
Abstract
The immune system is a dynamic network of diverse cell types distributed across tissues. While mouse studies have highlighted the importance of tissue-localized B-cell responses in infection and tissue repair, research on human B cells has remained largely confined to peripheral blood. Here, we specifically investigated the human B-cell compartment and its interactions with the immune microenvironment across 10 tissues, using single-cell RNA sequencing and paired B-cell receptor sequencing. We mapped the full spectrum of B-cell populations and revealed diverse differentiation trajectories spanning naive, memory, and plasma cell types. Germinal center B cells and plasma cells showed tissue-specific adaptations in transcriptional states, isotype usage, and functional profiles. Plasma cell isotypes influenced both effector functions and predicted interactions with T cells. Finally, we defined tissue-specific residency gene modules that outperformed existing memory B-cell signatures. Together, this dataset serves as a foundation for systematically studying tissue-localized B cells and reveals how local microenvironments shape humoral immunity.
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de Campos Mata, L., Yong, S., Du, L., Wan, H., Marani, E., Nilsen, V., Sekine, T., Marchalot, A., Tibbitt, C., Kammann, T., Mouchtaridi, E., Brownlie, D., Marquardt, N., Flodström-Tullberg, M., Sandberg, J. K., Lutolf, M. P., Cabon, L., Mjösberg, J., Jorns, C., Buggert, M., Hammarström, L., Ye, X., Pan-Hammarström, Q.. 2026-05-08. High-resolution single-cell atlas of the human B cell compartment and immune microenvironment across tissues. https://doi.org/10.64898/2026.05.05.722858
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