A single-cell cytokine dictionary of human peripheral blood
Oesinghaus, L.; Becker, S.; Vornholz, L.; Papalexi, E.; Pangallo, J.; Moinfar, A. A.; Liu, J.; Fleur, A. L.; Shulman, M.; Marrujo, S.; Hariadi, B.; Curca, C.; Suyama, A.; Nigos, M.; Sanderson, O.; Nguyen, H.; Tran, V. K.; Sapre, A. A.; Kaplan, O.; Schroeder, S.; Salvino, A.; Gallareta-Olivares, G.; Koehler, R.; Geiss, G.; Rosenberg, A. B.; Roco, C. M.; Seelig, G.; Theis, F.
Show abstract
Cytokines orchestrate immune responses, yet we still lack a comprehensive understanding of their specific effects across human immune cells due to their pleiotropy, context dependence and extensive functional redundancy. Here, we present a Human Cytokine Dictionary, created from high-resolution single-cell transcriptomes of 9,697,974 human peripheral blood mononuclear cells (PBMC) from 12 donors stimulated in vitro with 90 different cytokines. We describe donor-specific response variation and uncover robust consensus cytokine signatures across individuals. We then delineate similarities between cytokine response profiles, and derive cytokine-induced immune programs that organize responsive genes into data-driven, biologically interpretable functional modules. By integrating cell type-specific responses with expression of cytokines, we infer higher-order cell-to-cell and cytokine-to-cytokine communication networks exemplified by an IL-32-{beta}-initiated signaling cascade, which rewires myeloid programs by inducing neutrophil-recruiting factors while suppressing Th1-responses and promoting IL-10-family cytokines. Finally, we show how the Human Cytokine Dictionary enables the interpretation of cytokine-driven immune responses in other studies and disease contexts, including systemic lupus erythematosus, multiple sclerosis, and non-small cell lung carcinoma. Together, the Human Cytokine Dictionary constitutes the first comprehensive cell type-resolved transcriptional screen of human cytokine responses and provides an essential open-access, easy-to-use community resource with accompanying software package to advance our understanding of cytokine biology in human disease and guide therapeutic discovery.
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