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Role of IL-6 in the commitment of T cell subsets
被引:52
|作者:
Korn, Thomas
[1
,2
,3
]
Hiltensperger, Michael
[1
]
机构:
[1] Tech Univ Munich, Klinikum Rechts Isar, Inst Expt Neuroimmunol, Ismaninger Str 22, D-81675 Munich, Germany
[2] Tech Univ Munich, Klinikum Rechts Isar, Dept Neurol, Ismaninger Str 2, D-81675 Munich, Germany
[3] Munich Cluster Syst Neurol SyNergy, Feodor Lynen Str 17, D-81377 Munich, Germany
来源:
关键词:
IL-6;
Th17;
cell;
T follicular helper cell;
Treg cell;
IL-6 cluster signaling;
Host defence;
Autoimmunity;
SOLUBLE INTERLEUKIN-6 RECEPTOR;
NEUROMYELITIS-OPTICA;
TGF-BETA;
T(H)17 CELLS;
TH17;
CELLS;
GENERATION;
PLASTICITY;
RESPONSES;
CYTOKINE;
DIFFERENTIATION;
D O I:
10.1016/j.cyto.2021.155654
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
IL-6 gained much attention with the discovery that this cytokine is a non-redundant differentiation factor for Th17 cells and T follicular helper cells. Adaptive immune responses to fungi and extracellular bacteria are impaired in the absence of IL-6. IL-6 is also required for the induction of ROR-gamma t+ Treg cells, which are gatekeepers of homeostasis in the gut lamina propria in the presence of commensal bacteria. Conversely, severe immunopathology in T cell-mediated autoimmunity is mediated by Th17 cells that rely on IL-6 for their generation and maintenance. Recently, it has been discovered that the differentiation of these distinct T helper cell subsets may be linked to distinct signaling modalities of IL-6. Here, we summarize the current knowledge on the mode of action of IL-6 in the differentiation and maintenance of T cell subsets and propose that a contextdependent understanding of the impact of IL-6 on T cell subsets might inform rational IL-6-directed interventions in autoimmunity and chronic inflammation.
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