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IL-23 调控关节炎中的免疫细胞激活。

IL-23 orchestrating immune cell activation in arthritis.

机构信息

Institute of Infection, Immunity and Inflammation, College of Medical Veterinary and Life Sciences, University of Glasgow, Glasgow, UK.

出版信息

Rheumatology (Oxford). 2021 Oct 19;60(Suppl 4):iv4-iv15. doi: 10.1093/rheumatology/keab266.

Abstract

IL-23 is a cytokine member of the IL-12 superfamily. These heterodimeric cytokines offer broad immune regulatory activity with potential effector function in inflammatory arthritis. IL-23 is a pro-inflammatory cytokine secreted by dendritic cells and macrophages. It plays a key role in both innate and adaptive immunity. By promoting and maintaining T cell differentiation into Th17 T cells, IL-23 is a key player in the pathogenesis of rheumatic diseases. Data from pre-clinical IL-23 knockout models show the major importance of IL-23 in development of arthritis. The induction and maintenance of type 17 cells, which secrete IL-17A and other pro-inflammatory cytokines, contributes to local synovial inflammation and skin inflammation in PsA, and perhaps in RA. Commensurate with this, therapeutic strategies targeting IL-23 have proven efficient in PsA in several studies, albeit not yet in RA.

摘要

白细胞介素-23(IL-23)是白细胞介素-12 超家族的细胞因子成员。这些异二聚体细胞因子具有广泛的免疫调节活性,在炎症性关节炎中具有潜在的效应功能。白细胞介素-23 是树突状细胞和巨噬细胞分泌的促炎细胞因子。它在先天免疫和适应性免疫中都起着关键作用。通过促进和维持 T 细胞向 Th17 T 细胞的分化,白细胞介素-23 是风湿性疾病发病机制中的关键因素。来自临床前白细胞介素-23 敲除模型的数据表明,白细胞介素-23 在关节炎发展中的重要性。17 型细胞的诱导和维持,其分泌白细胞介素-17A 和其他促炎细胞因子,有助于 PsA 中的局部滑膜炎症和皮肤炎症,也许在 RA 中也是如此。与此相一致的是,针对白细胞介素-23 的治疗策略已被证明在几项 PsA 研究中有效,尽管尚未在 RA 中得到证实。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/334e/8527242/2196db849c7f/keab266f1.jpg

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