dc.creatorUniversidad San Sebastián
dc.creatorUniversidad San Sebastián
dc.creatorUniversidad San Sebastián
dc.creatorUniversidad San Sebastián
dc.creatorUniversidad San Sebastián
dc.creatorUniversidad San Sebastián
dc.creatorUniversidad San Sebastián
dc.creatorUniversidad San Sebastián
dc.creatorBourdely, Pierre
dc.creatorAnselmi, Giorgio
dc.creatorVaivode, Kristine
dc.creatorRamos, Rodrigo Nalio
dc.creatorMissolo-Koussou, Yoann
dc.creatorHidalgo, Sofia
dc.creatorTosselo, Jimena
dc.creatorNuñez, Nicolas
dc.creatorRicher, Wilfrid
dc.creatorVincent-Salomon, Anne
dc.creatorSaxena, Alka
dc.creatorWood, Kristie
dc.creatorLladser, Alvaro
dc.creatorPiaggio, Eliane
dc.creatorHelft, Julie
dc.creatorGuermonprez, Pierre
dc.date.accessioned2023-05-24T04:26:34Z
dc.date.available2023-05-24T04:26:34Z
dc.date.created2023-05-24T04:26:34Z
dc.date.issued2020-08-18
dc.identifier1074-7613
dc.identifierhttps://repositorio.uss.cl/handle/uss/4219
dc.identifier10.1016/j.immuni.2020.06.002
dc.description.abstractBourdely et al. identify human CD88−CD1c+CD163+ DC3s as a pro-inflammatory phagocyte lineage sharing features with monocytes and conventional DCs. DC3s efficiently induce differentiation of CD103+CD8+ T cells in vitro, and their infiltration correlates with CD8+CD69+CD103+ TRM accumulation in breast tumors.
dc.languageeng
dc.relationImmunity
dc.titleTranscriptional and Functional Analysis of CD1c+ Human Dendritic Cells Identifies a CD163+ Subset Priming CD8+CD103+ T Cells
dc.typeArtículo


Este ítem pertenece a la siguiente institución