The Chemokine, CCL20, and Its Receptor, CCR6, in the Pathogenesis and Treatment of Psoriasis and Psoriatic Arthritis.

autoimmune disease cell signaling chemokines migration psoriasis

Journal

Journal of psoriasis and psoriatic arthritis
ISSN: 2475-5311
Titre abrégé: J Psoriasis Psoriatic Arthritis
Pays: United States
ID NLM: 101695066

Informations de publication

Date de publication:
Jul 2023
Historique:
medline: 1 7 2023
pubmed: 1 7 2023
entrez: 19 9 2024
Statut: ppublish

Résumé

Chemokines represent a superfamily of immune-modulatory small protein molecules that regulate leukocyte migration to inflammatory sites through their chemoattractant and cell signaling properties. This review focuses on the immunological functions of the CCR6 chemokine receptor and is chemokine ligand, CCL20, that contribute to it role in inflammation in human psoriasis. Peer-reviewed relevant articles are searched and selected from 2000 to 2022 using the search engines including PubMed and Google Scholar. After selectively reviewing and evaluating over seventy articles, a comprehensive overview on the immunology of CCL20-CCR6 axis in psoriasis and psoriatic arthritis, the X-ray crystal structures of CCL20 monomers, and the potential of developing clinical therapies targeting this axis is summarized. Over the past decade, preclinical studies carried out in animal models of psoriasis involving agents targeting CCL20-CCR6 axis have yielded promising results. Other studies that this axis may play a role in a number of other autoimmune diseases, including rheumatoid arthritis, suggesting a rationale for further investigation into this key signaling/migratory pathway.

Sections du résumé

Background UNASSIGNED
Chemokines represent a superfamily of immune-modulatory small protein molecules that regulate leukocyte migration to inflammatory sites through their chemoattractant and cell signaling properties. This review focuses on the immunological functions of the CCR6 chemokine receptor and is chemokine ligand, CCL20, that contribute to it role in inflammation in human psoriasis.
Methods UNASSIGNED
Peer-reviewed relevant articles are searched and selected from 2000 to 2022 using the search engines including PubMed and Google Scholar.
Results UNASSIGNED
After selectively reviewing and evaluating over seventy articles, a comprehensive overview on the immunology of CCL20-CCR6 axis in psoriasis and psoriatic arthritis, the X-ray crystal structures of CCL20 monomers, and the potential of developing clinical therapies targeting this axis is summarized.
Conclusions UNASSIGNED
Over the past decade, preclinical studies carried out in animal models of psoriasis involving agents targeting CCL20-CCR6 axis have yielded promising results. Other studies that this axis may play a role in a number of other autoimmune diseases, including rheumatoid arthritis, suggesting a rationale for further investigation into this key signaling/migratory pathway.

Identifiants

pubmed: 39296310
doi: 10.1177/24755303231159106
pii: 10.1177_24755303231159106
pmc: PMC11361516
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

107-117

Informations de copyright

© The Author(s) 2023.

Déclaration de conflit d'intérêts

The author(s) declared the following potential conflicts of interest with respect to the research, authorship, and/or publication of this article: STH, BFV, and FCP have financial interest in and are officers of XLock Biosciences, which produces the CCL20LD.

Auteurs

Zhen-Rui Shi (ZR)

Department of Dermatology, Sun Yat-sen Memorial Hospital, Guang-zhou, China.

Tomotaka Mabuchi (T)

Department of Dermatology, Tokai University School of Medicine, Isehara, Japan.

Sarah J Riutta (SJ)

Department of Biochemistry, Medical College of Wisconsin, Milwaukee, WI, USA.

Xuesong Wu (X)

Department of Dermatology, University of California Davis School of Medicine, Sacramento, CA, USA.

Francis C Peterson (FC)

Department of Biochemistry, Medical College of Wisconsin, Milwaukee, WI, USA.

Brian F Volkman (BF)

Department of Biochemistry, Medical College of Wisconsin, Milwaukee, WI, USA.

Sam T Hwang (ST)

Department of Dermatology, University of California Davis School of Medicine, Sacramento, CA, USA.

Classifications MeSH