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- W2114872137 endingPage "538" @default.
- W2114872137 startingPage "505" @default.
- W2114872137 abstract "Mammalian lymphoid immunity is mediated by fast and slow responders to pathogens. Fast innate lymphocytes are active within hours after infections in mucosal tissues. Slow adaptive lymphocytes are conventional T and B cells with clonal antigen receptors that function days after pathogen exposure. A transcription factor (TF) regulatory network guiding early T cell development is at the core of effector function diversification in all innate lymphocytes, and the kinetics of immune responses is set by developmental programming. Operational units within the innate lymphoid system are not classified by the types of pathogen-sensing machineries but rather by discrete effector functions programmed by regulatory TF networks. Based on the evolutionary history of TFs of the regulatory networks, fast effectors likely arose earlier in the evolution of animals to fortify body barriers, and in mammals they often develop in fetal ontogeny prior to the establishment of fully competent adaptive immunity." @default.
- W2114872137 created "2016-06-24" @default.
- W2114872137 creator A5062608381 @default.
- W2114872137 creator A5069181181 @default.
- W2114872137 date "2015-03-21" @default.
- W2114872137 modified "2023-10-18" @default.
- W2114872137 title "Transcription Factor Networks Directing the Development, Function, and Evolution of Innate Lymphoid Effectors" @default.
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