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冠状动脉疾病中靶向白细胞介素-27的最新见解

Recent Insights Into Targeting Interleukin-27 in Coronary Artery Disease.

作者信息

Liang Wei-Lin, Liu Liang, Liang Bo

机构信息

Department of Cardiology, Guangyuan Hospital of Chinese Medicine, Guangyuan, China.

Department of Nephrology, Chongqing Key Laboratory of Prevention and Treatment of Kidney Disease, Chongqing Clinical Research Center of Kidney and Urology Diseases, Xinqiao Hospital, Army Medical University (Third Military Medical University), Chongqing, China.

出版信息

J Cardiovasc Transl Res. 2025 Jul 7. doi: 10.1007/s12265-025-10656-5.

Abstract

Coronary artery disease (CAD) is increasingly recognized as a chronic inflammatory condition. Interleukin-27 (IL-27), a cytokine from the IL-12 and IL-6 families, plays a dual role in CAD pathogenesis. It exacerbates disease by interacting with IL-1β and activating the NLRP3 inflammasome, promoting inflammation and tissue damage. Conversely, IL-27 can delay disease progression by engaging STAT1/3 signalling, suppressing inflammation, and promoting tissue repair. Future research should focus on elucidating IL-27's specific biological functions, interactions with molecular targets, and clinical implications in CAD. This will enhance understanding of CAD and support the development of improved diagnostic and therapeutic strategies.

摘要

冠状动脉疾病(CAD)越来越被认为是一种慢性炎症性疾病。白细胞介素-27(IL-27)是一种来自IL-12和IL-6家族的细胞因子,在CAD发病机制中起双重作用。它通过与IL-1β相互作用并激活NLRP3炎性小体来加重疾病,促进炎症和组织损伤。相反,IL-27可以通过参与STAT1/3信号传导、抑制炎症和促进组织修复来延缓疾病进展。未来的研究应集中于阐明IL-27在CAD中的具体生物学功能、与分子靶点的相互作用以及临床意义。这将增进对CAD的理解,并支持改进诊断和治疗策略的开发。

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