2025/04/15 by Huan Zhang, B. J. Yang Lee, Tong Wang +10 · 1 voice
Biochemistry, Genetics and Molecular Biology · Medicine · Neuroscience · #Dietary Effects on Health #Gut microbiota and health #Tryptophan and brain disorders
paper · doi:10.1016/j.hlife.2025.04.004
openalex publication_date 2025/04/15 · openalex created_date 2025/04/16 · openalex updated_date 2026/07/23
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. • Proposed “inflammatome” (holistic inflammation network) & “inflammatomics” (decoding dysbiosis-driven chronic inflammation). • Microbiota–immune crosstalk modulates inflammation and disease progression, informing targeted therapeutic strategies. • Chronic inflammation underlies metabolic/neurodegenerative disorders, revealing shared pathomechanisms. • Inflammatomics enables precision medicine via early detection, personalized interventions, and predictive biomarkers.