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Updated: Apr 7, 2026

Author Spotlight: Unveiling the Polyfunctionality and Heterogeneity in Immune Responses
Published on: March 8, 2024
Eicosanoid storm in infection and inflammation.
Edward A Dennis1, Paul C Norris1
1Department of Chemistry and Biochemistry and Department of Pharmacology, School of Medicine, University of California at San Diego, La Jolla, California 92093, USA.
Immune responses involve complex lipid mediator networks. Recent lipidomics research reveals eicosanoids and docosanoids with anti-inflammatory roles, advancing understanding of inflammation and its treatment.
Area of Science:
- Immunology
- Lipidomics
- Molecular Signaling
Background:
- Immune responses to infection and injury rely on intricate molecular signaling networks.
- Eicosanoids, derived from polyunsaturated fatty acids, form a complex bioactive lipid signaling network.
- Historically viewed as pro-inflammatory, eicosanoids also possess anti-inflammatory and pro-resolution functions.
Purpose of the Study:
- To review the dual role of eicosanoids in immune responses.
- To highlight advances in lipidomics for understanding eicosanoid signaling.
- To discuss the induction of eicosanoid storms by infectious agents.
Main Methods:
- Review of current literature on eicosanoid and docosanoid signaling.
- Analysis of lipidomics data in the context of immune responses.
- Examination of inflammatory receptor activation by infectious agents.
Main Results:
- Eicosanoid signaling networks are complex, with both pro-inflammatory and anti-inflammatory mediators.
- Lipidomics has identified novel eicosanoids and docosanoids with crucial anti-inflammatory functions.
- Infectious agents can induce a "storm" of pro- and anti-inflammatory eicosanoids via receptor activation.
Conclusions:
- Eicosanoid and docosanoid signaling are critical regulators of the immune response.
- Understanding these lipid mediators offers therapeutic potential for inflammatory conditions.
- The dual role of eicosanoids necessitates a nuanced view of their contribution to immunity.
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