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Interleukin-6 in non-infectious uveitis: Biology, experimentalevidence and treatment strategies.

作者信息

Yu Xiaoyang, Duan Runping, Jiang Loujing, Wang Tianfu, Li Zhaohuai, Zhang Bowen, Su Wenru, Lin Ying

机构信息

Guangzhou University of Chinese Medicine, Guangzhou 510060, China.

State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou 510060, China.

出版信息

Biochem Pharmacol. 2024 Dec;230(Pt 2):116605. doi: 10.1016/j.bcp.2024.116605. Epub 2024 Nov 2.

DOI:10.1016/j.bcp.2024.116605
PMID:39491564
Abstract

Uveitis is the leading cause of visual impairment worldwide. Interleukin-6 (IL-6), which is upregulated in response to inflammation, is one of the most important inflammatory cytokines associated with uveitis. Two major IL-6 receptors (IL-6R) mediate the pro-inflammatory and anti-inflammatory biological effects of IL-6. This review summarized multiple perspectives on the mechanism of IL-6-mediated uveitis, based on experimental evidence from clinical and animal models. It includes discussions on the roles of the downstream IL-6 signaling pathway, immunocytes, and the blood-retinal barrier. Therapeutic strategies aimed at blocking the action of IL-6 have progressed in clinical practice. However, due to the adverse events associated with existing biologics including infections, drugs that selectively inhibit intraocular IL-6 still require further development. The novel concept of converting the pro-inflammatory effects of IL-6 into protective effects also requires further research. In addition, the relationship between the trans-presentation of IL-6R and T-helper17 cells in uveitis remains unexplored. This review aims to consolidate our current understanding of the biology, signaling pathways, experimental models, and immune pathogenesis related to IL-6 and uveitis. We also discuss clinical strategies focused on blocking IL-6 as a treatment for uveitis. Targeting IL-6 provides unlimited potential for improving the diagnosis, treatment, and prognosis of uveitis.

摘要

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引用本文的文献

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