作者
Ramon Massoni-Badosa,Sergio Aguilar-Fernández,Juan C. Nieto,Paula Soler-Vila,Marc Elosua-Bayés,Doménica Marchese,Marta Kulis,Amaia Vilas‐Zornoza,Marco M. Bühler,Sonal Rashmi,Clara Alsinet,Ginevra Caratù,Cátia Moutinho,Sara Ruiz,Patricia Lorden,Giulia Lunazzi,Dolors Colomer,Gerard Frigola,Will Blevins,Lucia Romero-Rivero,Víctor Jiménez-Martínez,Anna Vidal,Judith Mateos-Jaimez,Alba Maiqués-Díaz,Sara Ovejero,Jérôme Moreaux,Sara Palomino,David Gómez-Cabrero,Xabier Agirre,Marc A. Weniger,Hamish W. King,Lucy C. Garner,Fédérico Marini,Francisco Javier Cervera‐Paz,Peter Baptista,Isabel Vilaseca,Cecilia Rosales,Sílvia Ruiz-Gaspà,Benjamin James Talks,Keval Sidhpura,Anna Pascual Reguant,Anja E. Hauser,Muzlifah Haniffa,Felipe Prósper,Ralf Küppers,Marta Gut,Elı́as Campo,José I. Martín‐Subero,Holger Heyn
摘要
Palatine tonsils are secondary lymphoid organs (SLOs) representing the first line of immunological defense against inhaled or ingested pathogens. We generated an atlas of the human tonsil composed of >556,000 cells profiled across five different data modalities, including single-cell transcriptome, epigenome, proteome, and immune repertoire sequencing, as well as spatial transcriptomics. This census identified 121 cell types and states, defined developmental trajectories, and enabled an understanding of the functional units of the tonsil. Exemplarily, we stratified myeloid slan-like subtypes, established a BCL6 enhancer as locally active in follicle-associated T and B cells, and identified SIX5 as putative transcriptional regulator of plasma cell maturation. Analyses of a validation cohort confirmed the presence, annotation, and markers of tonsillar cell types and provided evidence of age-related compositional shifts. We demonstrate the value of this resource by annotating cells from B cell-derived mantle cell lymphomas, linking transcriptional heterogeneity to normal B cell differentiation states of the human tonsil.