2023
DOI: 10.1016/j.coi.2023.102296
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Inborn errors of human transcription factors governing IFN-γ antimycobacterial immunity

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Cited by 8 publications
(2 citation statements)
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“…Of note, IRF8 is a member of a family of nine transcription factors characterized by a conserved N‐terminal domain 16,36,37 . Although STAT1 is expressed widely, IRF8 expression is observed in lymphoid‐cell lineages as well as in various other tissue types, including the brain and heart 38–40 . IFNγ and TLR4‐A are key factors in starting atherosclerosis and plaque formation by activating STAT and IRF transcription factors that regulate the immune response 41–44 .…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Of note, IRF8 is a member of a family of nine transcription factors characterized by a conserved N‐terminal domain 16,36,37 . Although STAT1 is expressed widely, IRF8 expression is observed in lymphoid‐cell lineages as well as in various other tissue types, including the brain and heart 38–40 . IFNγ and TLR4‐A are key factors in starting atherosclerosis and plaque formation by activating STAT and IRF transcription factors that regulate the immune response 41–44 .…”
Section: Discussionmentioning
confidence: 99%
“…16,36,37 Although STAT1 is expressed widely, IRF8 expression is observed in lymphoidcell lineages as well as in various other tissue types, including the brain and heart. [38][39][40] IFNγ and TLR4-A are key factors in starting atherosclerosis and plaque formation by activating STAT and IRF transcription factors that regulate the immune response. [41][42][43][44] Specifically, STAT1 and IRF8 have emerged as key regulators of inflammation, particularly within immune cell populations.…”
Section: In Vitro Experiments Validated the Role Of Irf8 As An Immune...mentioning
confidence: 99%