AI Article Synopsis

  • Non-resolving inflammation significantly contributes to health issues in cystic fibrosis (CF), a severe genetic disorder.
  • Specialized pro-resolving lipid mediators (SPMs) like lipoxins, resolvins, protectins, and maresins play a crucial role in managing inflammation by promoting healing and reducing harmful immune responses.
  • Research indicates that SPMs might serve as promising non-immunosuppressive treatments to improve inflammation and infection control in CF patients, highlighting the potential for new therapeutic strategies.

Article Abstract

Non-resolving inflammation is the main mechanism of morbidity and mortality among patients suffering from cystic fibrosis (CF), the most common life-threatening human genetic disease. Resolution of inflammation is an active process timely controlled by endogenous specialized pro-resolving lipid mediators (SPMs) produced locally in inflammatory loci to restrain this innate response, prevent further damages to the host, and permit return to homeostasis. Lipoxins, resolvins, protectins, and maresins are SPM derived from polyunsaturated fatty acids that limit excessive leukocyte infiltration and pro-inflammatory signals, stimulate innate microbial killing, and enhance resolution. Their unique chemical structures, receptors, and bioactions are being elucidated. Accruing data indicate that SPMs carry protective functions against unrelenting inflammation and infections in preclinical models and human CF systems. Here, we reviewed their roles and actions in controlling resolution of inflammation, evidence for their impairment in CF, and proofs of principle for their exploitation as innovative, non-immunosuppressive drugs to address inflammation and infections in CF.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6454233PMC
http://dx.doi.org/10.3389/fphar.2019.00252DOI Listing

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