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社区获得性肺炎中的白细胞介素:从生物标志物到精准医学

Interleukins in Community-Acquired Pneumonia: From Biomarkers to Precision Medicine

Frontiers in Oncology 等信源发布 2026-02-06 08:02

可切换为仅中文


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Community-acquired pneumonia (CAP) is still a leading cause of death due to infection globally, yet precise severity assessment remains a significant clinical problem. More than any other group of cytokines, interleukins are central to the regulation of inflammation and shed light on this intricate pathology.

社区获得性肺炎(CAP)仍然是全球范围内因感染导致死亡的主要原因之一,但精确的严重程度评估仍然是一个重要的临床问题。在所有细胞因子中,白细胞介素对炎症调节起着核心作用,并为这一复杂的病理过程提供了重要线索。

In the present review we summarize the biological and clinical characteristics of some of the principal interleukins (ILs) in CAP, classified primarily according to their physiological activity as pro-inflammatory (IL-2, IL-6, IL-8 and IL-12), anti-inflammatory (IL-7, IL-10 and IL-37), dual-action (IL-4 and IL-17), and emerging factors (IL-3, IL-27 and IL-33).

在本综述中,我们总结了一些主要白细胞介素(ILs)在CAP中的生物学和临床特征,主要根据其生理活性分类为促炎型(IL-2、IL-6、IL-8和IL-12)、抗炎型(IL-7、IL-10和IL-37)、双重作用型(IL-4和IL-17)以及新兴因子(IL-3、IL-27和IL-33)。

Additionally, recent multimodal approaches are discussed such as combining cytokines with organ dysfunction parameters (MR-proADM) or revealing host-response patterns to inform antibiotic and corticosteroid management. We propose that the field needs to transition to immunological endotyping, multi-omics (integrating genetics and lung microbiome), and artificial intelligence (AI) models based on dynamic patient data to achieve precision medicine in CAP management..

此外,还讨论了最近的多模式方法,例如将细胞因子与器官功能障碍参数(MR-proADM)结合,或揭示宿主反应模式以指导抗生素和皮质类固醇的管理。我们认为,该领域需要过渡到免疫学内型、多组学(整合遗传学和肺微生物组)以及基于动态患者数据的人工智能(AI)模型,以实现CAP管理中的精准医学。