Immune Modulation of Monocytes Dampens the IL-17
Animals
Antigens, Ly
/ metabolism
Disease Models, Animal
Humans
Imiquimod
/ administration & dosage
Immunologic Factors
/ pharmacology
Interleukin-17
/ metabolism
Interleukin-1beta
/ metabolism
Interleukin-23
/ metabolism
Intraepithelial Lymphocytes
/ immunology
Macrophages
/ immunology
Male
Mice
Monocytes
/ drug effects
Psoriasis
/ chemically induced
Severity of Illness Index
Skin
/ cytology
Journal
The Journal of investigative dermatology
ISSN: 1523-1747
Titre abrégé: J Invest Dermatol
Pays: United States
ID NLM: 0426720
Informations de publication
Date de publication:
12 2020
12 2020
Historique:
received:
09
01
2020
revised:
12
03
2020
accepted:
17
03
2020
pubmed:
12
5
2020
medline:
2
4
2021
entrez:
12
5
2020
Statut:
ppublish
Résumé
Psoriasis is a chronic inflammatory autoimmune skin condition that affects millions of people worldwide. It is driven by IL-17-producing CD4 and γδ T cells and targeted by current anti-IL-17 or anti-IL-23 mAb therapies. These treatments are expensive, increase the risk of opportunistic infections, and do not specifically target the inflammatory cascade. Other cells, including inflammatory monocytes, have been shown to migrate to psoriatic plaques in both human disease and the imiquimod-induced mouse model and could thus constitute potential alternative therapeutic targets. In the mouse, immune modifying particles (IMPs) specifically target Ly6C
Identifiants
pubmed: 32389535
pii: S0022-202X(20)31456-1
doi: 10.1016/j.jid.2020.03.973
pii:
doi:
Substances chimiques
Antigens, Ly
0
IL1B protein, mouse
0
Immunologic Factors
0
Interleukin-17
0
Interleukin-1beta
0
Interleukin-23
0
Ly-6C antigen, mouse
0
Imiquimod
P1QW714R7M
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
2398-2407.e1Informations de copyright
Copyright © 2020 The Authors. Published by Elsevier Inc. All rights reserved.