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白细胞介素-6在炎症、自身免疫和癌症中的作用

IL-6 in inflammation, autoimmunity and cancer.

作者信息

Hirano Toshio

机构信息

National Institutes for Quantum and Radiological Science and Technology, Anagawa, Inage-ku, Chiba, Japan.

Division of Molecular Psychoimmunology, Institute for Genetic Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan.

出版信息

Int Immunol. 2021 Mar 1;33(3):127-148. doi: 10.1093/intimm/dxaa078.

Abstract

IL-6 is involved both in immune responses and in inflammation, hematopoiesis, bone metabolism and embryonic development. IL-6 plays roles in chronic inflammation (closely related to chronic inflammatory diseases, autoimmune diseases and cancer) and even in the cytokine storm of corona virus disease 2019 (COVID-19). Acute inflammation during the immune response and wound healing is a well-controlled response, whereas chronic inflammation and the cytokine storm are uncontrolled inflammatory responses. Non-immune and immune cells, cytokines such as IL-1β, IL-6 and tumor necrosis factor alpha (TNFα) and transcription factors nuclear factor-kappa B (NF-κB) and signal transducer and activator of transcription 3 (STAT3) play central roles in inflammation. Synergistic interactions between NF-κB and STAT3 induce the hyper-activation of NF-κB followed by the production of various inflammatory cytokines. Because IL-6 is an NF-κB target, simultaneous activation of NF-κB and STAT3 in non-immune cells triggers a positive feedback loop of NF-κB activation by the IL-6-STAT3 axis. This positive feedback loop is called the IL-6 amplifier (IL-6 Amp) and is a key player in the local initiation model, which states that local initiators, such as senescence, obesity, stressors, infection, injury and smoking, trigger diseases by promoting interactions between non-immune cells and immune cells. This model counters dogma that holds that autoimmunity and oncogenesis are triggered by the breakdown of tissue-specific immune tolerance and oncogenic mutations, respectively. The IL-6 Amp is activated by a variety of local initiators, demonstrating that the IL-6-STAT3 axis is a critical target for treating diseases.

摘要

白细胞介素-6(IL-6)参与免疫反应、炎症、造血、骨代谢和胚胎发育。IL-6在慢性炎症(与慢性炎症性疾病、自身免疫性疾病和癌症密切相关)甚至2019冠状病毒病(COVID-19)的细胞因子风暴中发挥作用。免疫反应和伤口愈合过程中的急性炎症是一种受到良好控制的反应,而慢性炎症和细胞因子风暴则是不受控制的炎症反应。非免疫细胞和免疫细胞、细胞因子如白细胞介素-1β(IL-1β)、IL-6和肿瘤坏死因子-α(TNFα)以及转录因子核因子-κB(NF-κB)和信号转导及转录激活因子3(STAT3)在炎症中起核心作用。NF-κB和STAT3之间的协同相互作用诱导NF-κB的过度激活,随后产生各种炎症细胞因子。由于IL-6是NF-κB的靶标,非免疫细胞中NF-κB和STAT3的同时激活通过IL-6-STAT3轴触发NF-κB激活的正反馈回路。这种正反馈回路称为IL-6放大器(IL-6 Amp),是局部起始模型中的关键因素,该模型指出衰老、肥胖、应激源、感染、损伤和吸烟等局部起始因素通过促进非免疫细胞与免疫细胞之间的相互作用引发疾病。该模型与认为自身免疫和肿瘤发生分别由组织特异性免疫耐受的破坏和致癌突变引发的教条相反。IL-6 Amp被多种局部起始因素激活,表明IL-6-STAT3轴是治疗疾病的关键靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ac9/7936067/b752287f5854/dxaa078_fig1.jpg

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