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Resolution of inflammation: An organizing principle in biology and medicine

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PHARMACOLOGY & THERAPEUTICS
卷 227, 期 -, 页码 -

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PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.pharmthera.2021.107879

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资金

  1. NIH [R24 DA018055, R01GM123508, R01GM038765]
  2. NIH Credit Unions Kids at Heart Team
  3. C.J. Buckley Pediatric Brain Tumor Fund
  4. Joe Andruzzi Foundation
  5. Professional Staff Congress-City University of New York (PSC-CUNY) [TRADB-49-271]

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The resolution of inflammation is a critical endogenous process that protects host tissues from chronic inflammation, with failure of resolution being a key mechanism for progression of inflammation-driven diseases. Specialized pro-resolving mediators derived from essential polyunsaturated fatty acids regulate endogenous resolution programs by limiting neutrophil infiltration and promoting immune cell-mediated clearance, highlighting their therapeutic potential across various inflammatory diseases including cancer.
The resolution of inflammation has emerged as a critical endogenous process that protects host tissues from prolonged or excessive inflammation that can become chronic. Failure of the resolution of inflammation is a key pathological mechanism that drives the progression of numerous inflammation-driven diseases. Essential polyunsaturated fatty acid (PUFA)-derived autacoid mediators termed 'specialized pro-resolving mediators' (SPMs) regulate endogenous resolution programs by limiting further neutrophil tissue infiltration and stimulating local immune cell (e.g., macrophage)-mediated clearance of apoptotic polymorphonuclear neutrophils, cellular debris, and microbes, as well as counter-regulating eicosanoid/cytokine production. The SPM superfamily encompasses lipoxins, resolvins, protectins, and maresins. Our understanding of the resolution phase of acute inflammation has grown exponentially in the past three decades with the discovery of novel pro-resolving lipid mediators, their pro-efferocytosis mechanisms, and their receptors. Technological advancement has further facilitated lipid mediator metabolipidomic based profiling of healthy and diseased human tissues, highlighting the extraordinary therapeutic potential of SPMs across a broad array of inflammatory diseases including cancer. As current front-line cancer therapies such as surgery, chemotherapy, and radiation may induce various unwanted side effects such as robust pro-inflammatory and pro-tumorigenic host responses, characterizing SPMs and their receptors as novel therapeutic targets may have important implications as a new direction for host targeted cancer therapy. Here, we discuss the origins of inflammation resolution, key discoveries and the failure of resolution mechanisms in diseases with an emphasis on cancer, and future directions focused on novel therapeutic applications for this exciting and rapidly expanding field. (C) 2021 Elsevier Inc. All rights reserved.

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