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Single-cell RNA sequencing reveals induction of distinct trained-immunity programs in human monocytes

Trained immunity refers to the long-lasting memory traits of innate immunity. Recent studies have shown that trained immunity is orchestrated by sustained changes in epigenetic marks and metabolic pathways, leading to an altered transcriptional response to a second challenge. However, the potential...

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Detalles Bibliográficos
Autores principales: Zhang, Bowen, Moorlag, Simone J.C.F.M, Dominguez-Andres, Jorge, Bulut, Özlem, Kilic, Gizem, Liu, Zhaoli, van Crevel, Reinout, Xu, Cheng-Jian, Joosten, Leo A.B., Netea, Mihai G., Li, Yang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Clinical Investigation 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8970681/
https://www.ncbi.nlm.nih.gov/pubmed/35133977
http://dx.doi.org/10.1172/JCI147719
Descripción
Sumario:Trained immunity refers to the long-lasting memory traits of innate immunity. Recent studies have shown that trained immunity is orchestrated by sustained changes in epigenetic marks and metabolic pathways, leading to an altered transcriptional response to a second challenge. However, the potential heterogeneity of trained-immunity induction in innate immune cells has not been explored. In this study, we demonstrate cellular transcriptional programs in response to 4 different inducers of trained immunity in monocyte populations at single-cell resolution. Specifically, we identified 3 monocyte subpopulations upon the induction of trained immunity, and replicated these findings in an in vivo study. In addition, we found gene signatures consistent with these functional programs in patients with ulcerative colitis, sepsis, and COVID-19, suggesting the impact of trained-immunity programs in immune-mediated diseases.