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- W194928101 endingPage "27" @default.
- W194928101 startingPage "11" @default.
- W194928101 abstract "Naïve CD8 T cells differentiate in response to antigen stimulation. They acquire the capacity to express multiple effector molecules and mediate effector functions that contribute to infection control. Once antigen loads are reduced they revert progressively to a less activated status and eventually reach a steady-state referred to as memory that is very different from that of naive cells. Indeed, these memory cells are ready-to-go populations that acquired the capacity to respond more efficiently to antigen stimulation. They modify their cell cycle machinery in order to divide faster; they likely improve DNA repair and other cell survival mechanisms in order to survive during division and thus to generate much larger clones of effector cells; finally, they also mediate effector functions much faster. These modifications are the consequence of changes in the expression of multiple genes, i.e., on the utilization of a new transcription program." @default.
- W194928101 created "2016-06-24" @default.
- W194928101 creator A5037710215 @default.
- W194928101 creator A5055632646 @default.
- W194928101 creator A5058985066 @default.
- W194928101 creator A5080431922 @default.
- W194928101 date "2010-01-01" @default.
- W194928101 modified "2023-10-16" @default.
- W194928101 title "Transcriptional Regulation during CD8 T-Cell Immune Responses" @default.
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- W194928101 doi "https://doi.org/10.1007/978-1-4419-6451-9_2" @default.
- W194928101 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/20795537" @default.