2022
DOI: 10.1016/j.bbrc.2022.06.038
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IL-1R1 blockade attenuates liver injury through inhibiting the recruitment of myeloid-derived suppressor cells in sepsis

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Cited by 4 publications
(2 citation statements)
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“…CD247 is poorly expressed in septic mice [ 47 ] and is a promising target for the prognosis of sepsis in LPS-induced septic mice [ 48 ]. IL1R1 is upregulated in microglial cells of rats with sepsis-associated encephalopathy [ 49 ]; inhibiting IL1R1 can attenuate liver injury in septic mice [ 50 ]. CD28 expression is abnormally downregulated in sepsis, and activation of CD28 helps to improve the survival rate of septic mice [ 51 ].…”
Section: Discussionmentioning
confidence: 99%
“…CD247 is poorly expressed in septic mice [ 47 ] and is a promising target for the prognosis of sepsis in LPS-induced septic mice [ 48 ]. IL1R1 is upregulated in microglial cells of rats with sepsis-associated encephalopathy [ 49 ]; inhibiting IL1R1 can attenuate liver injury in septic mice [ 50 ]. CD28 expression is abnormally downregulated in sepsis, and activation of CD28 helps to improve the survival rate of septic mice [ 51 ].…”
Section: Discussionmentioning
confidence: 99%
“…The expression of IL-1R1 protein is known to regulate inflammation by facilitating the uptake of IL-1β [ 63 ]. IL1R1 has been implicated in various diseases, including liver injury [ 64 ], kidney injury [ 65 ], ischemic injury [ 36 ] and neurodegeneration [ 66 ]. Here, it was first verified that IL1R1 mediates microglial activation in TN.…”
Section: Discussionmentioning
confidence: 99%