Triggering the Resolution of Immune Mediated Inflammatory Diseases: Can Targeting Leukocyte Migration Be the Answer?

11-beta hydroxysteroid dehydrogenase PEPITEM glucocorticoids inflammation leukocytes migration resolution sphingosine-1-phosphate

Journal

Frontiers in pharmacology
ISSN: 1663-9812
Titre abrégé: Front Pharmacol
Pays: Switzerland
ID NLM: 101548923

Informations de publication

Date de publication:
2019
Historique:
received: 06 10 2018
accepted: 14 02 2019
entrez: 19 3 2019
pubmed: 19 3 2019
medline: 19 3 2019
Statut: epublish

Résumé

Leukocyte recruitment is a pivotal process in the regulation and resolution of an inflammatory episode. It is vital for the protective responses to microbial infection and tissue damage, but is the unwanted reaction contributing to pathology in many immune mediated inflammatory diseases (IMIDs). Indeed, it is now recognized that patients with IMIDs have defects in at least one, if not multiple, check-points regulating the entry and exit of leukocytes from the inflamed site. In this review, we will explore our understanding of the imbalance in recruitment that permits the accumulation and persistence of leukocytes in IMIDs. We will highlight old and novel pharmacological tools targeting these processes in an attempt to trigger resolution of the inflammatory response. In this context, we will focus on cytokines, chemokines, known pro-resolving lipid mediators and potential novel lipids (e.g., sphingosine-1-phosphate), along with the actions of glucocorticoids mediated by 11-beta hydroxysteroid dehydrogenase 1 and 2.

Identifiants

pubmed: 30881306
doi: 10.3389/fphar.2019.00184
pmc: PMC6407428
doi:

Types de publication

Journal Article

Langues

eng

Pagination

184

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Auteurs

Sophie J Hopkin (SJ)

Institute of Cardiovascular Sciences, University of Birmingham, Birmingham, United Kingdom.

Jonathan W Lewis (JW)

Rheumatology Research Group, Arthritis Research UK Centre of Excellence in the Pathogenesis of Rheumatoid Arthritis, Institute of Inflammation and Ageing, University of Birmingham, Birmingham, United Kingdom.

Franziska Krautter (F)

Institute of Cardiovascular Sciences, University of Birmingham, Birmingham, United Kingdom.

Myriam Chimen (M)

Institute of Cardiovascular Sciences, University of Birmingham, Birmingham, United Kingdom.

Helen M McGettrick (HM)

Rheumatology Research Group, Arthritis Research UK Centre of Excellence in the Pathogenesis of Rheumatoid Arthritis, Institute of Inflammation and Ageing, University of Birmingham, Birmingham, United Kingdom.

Classifications MeSH