训练免疫:脓毒症防治的免疫调控新策略OA
Trained immunity:A novel immunomodulatory strategy for sepsis prevention and treatment
脓毒症是一种由感染诱发、以宿主免疫反应失调为核心特征的危及生命的综合征,其病死率长期居高不下,是重症医学领域面临的重大挑战.传统治疗策略主要聚焦于抗感染和器官功能支持,对免疫失衡这一核心病理环节的干预手段有限,临床疗效亟待突破.近年来,"训练免疫"概念的提出及其分子机制的不断阐明,为脓毒症的防治提供了全新的理论基础.训练免疫是指先天免疫细胞在初次接受刺激后,通过代谢重编程和表观遗传重塑,获得增强或减弱的二次应答能力,从而形成一种非抗原特异性的免疫记忆.这一过程可通过增强宿主防御、提高病原体清除效率,在一定条件下对脓毒症的防治发挥积极作用.本文系统阐述了训练免疫的基本概念及其分子机制,重点阐述其在脓毒症发生、发展中的作用,并探讨基于训练免疫调控的新型治疗策略,旨在为脓毒症的精准免疫治疗提供理论依据和新思路.
Sepsis is a life-threatening syndrome triggered by infection,and characterized by a dysregulated host immune response.It remains a major challenge in critical care medicine with persistently high mortality rates.Traditional therapeutic strategies have focused mainly on anti-infection and organ support,offering limited interventions for the core pathological process of immune imbalance,leaving clinical efficacy in urgent need of breakthrough.In recent years,the concept of"trained immunity"and the ongoing elucidation of its molecular mechanisms have provided a novel theoretical foundation for the prevention and treatment of sepsis.Trained immunity refers to the ability of innate immune cells to develop enhanced or diminished secondary response capabilities after an initial stimulus,through metabolic reprogramming and epigenetic remodeling,thereby establishing a form of non-antigen-specific immune memory.This process may exert positive effects on sepsis management by enhancing host defense and improving pathogen clearance efficiency under certain conditions.This article systematically reviews the fundamental concepts and molecular mechanisms of trained immunity,with a focus on its role in the onset,progression,and outcome of sepsis.Furthermore,it explores novel therapeutic strategies based on the modulation of trained immunity,aiming to provide a theoretical basis and new perspectives for precise immunotherapy in sepsis.
刘靖华
南方医科大学基础医学院,广州 510515
训练免疫脓毒症免疫调控代谢重编程表观遗传修饰
trained immunitysepsisimmune regulationmetabolic reprogrammingepigenetic modification
《感染、炎症、修复》 2026 (2)
111-114,4
国家自然科学基金资助项目(82472199)
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