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Updated: May 19, 2026

Intravenous Endotoxin Challenge in Healthy Humans: An Experimental Platform to Investigate and Modulate Systemic Inflammation
Published on: May 16, 2016
The theory of the inflammatory ecosystem
Phei Er Saw1, Erwei Song2,3,4,5,6
1Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Guangdong-Hong Kong Joint Laboratory for RNA Medicine, Breast Tumor Center, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, 510120, China.
None:
Chronic inflammatory diseases are increasingly recognized as dynamic and spatially complex disorders involving diverse immune and nonimmune components. In this review, we introduce the concept of the inflammatory ecosystem as a framework for understanding how inflammation is organized across distinct anatomical and functional zones, termed inflammazones-ranging from local to systemic. We first examine how immune cells, through activation, differentiation, and mimicry, transition into inflammatory phenotypes. We then explore the transformation of non-immune cells-such as keratinocytes, fibroblasts, and endothelial cells-into active participants in inflammation, facilitated by intercellular crosstalk and cytokine exchange. Central to these processes are biophysical and molecular mechanisms such as phase separation, signalosome formation, and exosome-mediated communication, which organize and amplify inflammatory signals. We further delineate how these cellular events lead to pathological changes in organ-specific contexts, using diseases like sarcoidosis and psoriasis as model systems. Finally, we discuss the therapeutic implications of this ecosystem-based approach, highlighting how zone-specific interventions and multi-omics-guided precision medicine can transform the treatment landscape of inflammatory diseases. This conceptual model advances our understanding of inflammation as an integrated, spatially regulated process with broad clinical relevance.
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