微生物群,慢性炎症和健康:炎症组学和炎症组学对精准医学和卫生保健的承诺

hLife Pub Date : 2025-04-15 DOI:10.1016/j.hlife.2025.04.004
Huan Zhang , Bing Jun Yang Lee , Tong Wang , Xuesong Xiang , Yafang Tan , Yanping Han , Yujing Bi , Fachao Zhi , Xin Wang , Fang He , Seppo J. Salminen , Baoli Zhu , Ruifu Yang
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引用次数: 0

摘要

术语“炎症组”(整体炎症网络)和“炎症组学”(一个新的组学领域)被提出来解码生态失调驱动的慢性炎症及其疾病联系。炎症组学探索微生物群-免疫串扰,特别是先天免疫相互作用,揭示了失调的微生物群落如何引发慢性炎症潜在疾病,如炎症性肠病、代谢性疾病和神经变性。这门学科超越了传统的炎症范式,通过剖析连接生态失调和全身性炎症的分子途径,实现早期检测和精确干预。它整合了宿主-微生物相互作用的进化观点,强调人体是一个对压力敏感的“器官”。挑战包括标准化炎性组分析,将研究结果转化为临床工具,以及推进多组学技术。通过连接微生物生态学、免疫学和系统医学,炎症组学具有变革性的潜力,可以将医疗保健从被动治疗转变为主动、个性化的预防,针对慢性炎症体失调形成的疾病起源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Microbiota, chronic inflammation, and health: The promise of inflammatome and inflammatomics for precision medicine and health care

Microbiota, chronic inflammation, and health: The promise of inflammatome and inflammatomics for precision medicine and health care
The terms “inflammatome” (holistic inflammation networks) and “inflammatomics” (a novel omics field) were proposed to decode dysbiosis-driven chronic inflammation and its disease links. Inflammatomics explores microbiota–immune crosstalk, particularly innate immune interactions, revealing how dysregulated microbial communities trigger chronic inflammation underlying disorders like inflammatory bowel disease, metabolic diseases, and neurodegeneration. This discipline transcends traditional inflammation paradigms by dissecting molecular pathways connecting dysbiosis to systemic inflammation, enabling early detection and precision interventions. It integrates evolutionary perspectives on host–microbe interactions, emphasizing the human body as a stress-sensitive “organ”. Challenges include standardizing inflammatome profiling, translating findings into clinical tools, and advancing multiomics technologies. By bridging microbial ecology, immunology, and systems medicine, inflammatomics holds a transformative potential to shift health care from reactive treatment to proactive, personalized prevention, targeting disease origins shaped by chronic inflammatome dysregulation.
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