Fanzhou Ren, Yuding Luo, Pingchuan Liu, Hai Xiong, Xu Liu, Jian Wang
North Sichuan Medical College, Nanchong, China.
Department of Neurology, Ya'an People's Hospital, Ya'an, China.
Ann Med. 2025 Dec;57(1):2543519. doi: 10.1080/07853890.2025.2543519. Epub 2025 Aug 8.
Post-stroke cognitive impairment (PSCI) is a prevalent complication that impairs stroke survivors' quality of life and rehabilitation. Growing evidence highlights the crucial role of inflammation in PSCI pathogenesis. The tumor necrosis factor (TNF) signaling pathway, especially tumor necrosis factor-α (TNF-α), has gained attention for its role in neuroinflammatory diseases. TNF pathway activation is strongly associated with neuronal injury and neuroinflammation in stroke, suggesting its involvement in PSCI. However, the exact mechanisms by which TNF signaling contributes to PSCI remain unclear.
This review summarizes recent evidence on the TNF signaling pathway to elucidate its molecular mechanisms, analyze its role in PSCI pathogenesis, and examine associated inflammatory responses and their functional consequences. We also explores potential therapeutic targets, offering novel perspectives for PSCI intervention.
A comprehensive literature search was conducted across electronic databases including PubMed, Web of Science, Embase, and MEDLINE to identify relevant studies. We systematically reviewed recent research investigating the role and mechanisms of the TNF signaling pathway in PSCI. Eligible studies were rigorously screened, followed by data extraction and quality assessment using standardized criteria.
The TNF signaling pathway is complex and heterogeneous in PSCI, potentially attributable to variations in study designs, samples, experimental models, and interventions. Emerging evidence supports the therapeutic potential of pharmacological and biological agents targeting this pathway. These findings highlight the need for integrated clinical and basic research to strengthen the foundation for early diagnosis, prevention, and treatment of PSCI, and to guide evidence-based clinical decisions.
卒中后认知障碍(PSCI)是一种常见的并发症,会损害卒中幸存者的生活质量和康复效果。越来越多的证据表明炎症在PSCI发病机制中起关键作用。肿瘤坏死因子(TNF)信号通路,尤其是肿瘤坏死因子-α(TNF-α),因其在神经炎症性疾病中的作用而受到关注。TNF通路激活与卒中后的神经元损伤和神经炎症密切相关,提示其参与了PSCI的发生。然而,TNF信号通路导致PSCI的确切机制仍不清楚。
本综述总结了关于TNF信号通路的最新证据,以阐明其分子机制,分析其在PSCI发病机制中的作用,并研究相关的炎症反应及其功能后果。我们还探讨了潜在的治疗靶点,为PSCI的干预提供新的视角。
在包括PubMed、Web of Science、Embase和MEDLINE在内的电子数据库中进行了全面的文献检索,以识别相关研究。我们系统地回顾了最近关于TNF信号通路在PSCI中的作用和机制的研究。对符合条件的研究进行严格筛选,然后使用标准化标准进行数据提取和质量评估。
TNF信号通路在PSCI中是复杂且异质性的,这可能归因于研究设计、样本、实验模型和干预措施的差异。新出现的证据支持针对该通路的药理和生物制剂的治疗潜力。这些发现凸显了整合临床和基础研究的必要性,以加强PSCI早期诊断、预防和治疗的基础,并指导基于证据的临床决策。