Abstract |
Allergic diseases arise from a complex interplay between immune system and environmental factors. A link between the pathogenesis of allergic diseases and type 2 immune responses has become evident, with conventional and pathogenic type 2 helper T (Th2) cells involved in both. Recently, there has been a significant development in therapeutic agents for allergic diseases: IL-5 and IL-5 receptor antagonists, Janus kinase ( JAK) inhibitors, and sublingual immunotherapy (SLIT). Mepolizumab, an IL-5, and Benralizumab, an IL-5 receptor antagonist, modulate eosinophilic inflammation mediated by IL-5-producing Th2 cells. Delgocitinib shows that JAK-associated signaling is essential for the inflammatory reaction in atopic dermatitis, one of the common allergic diseases. SLIT has a significant effect on allergic rhinitis by reducing pathogenic Th2 cell numbers. More recently, novel molecules that are involved in pathogenic Th2 cell-mediated allergic diseases have been identified. These include calcitonin gene-related peptide (CGRP), reactive oxygen species (ROS) scavenging machinery regulated by the Txnip-Nrf2-Blvrb axis, and myosin light chain 9 (Myl9), which interacts with CD69. This review provides an updated view of the recent research on treatment of allergic diseases and their cause: conventional and pathogenic Th2 cells.
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Authors | Atsushi Onodera, Kota Kokubo, Mikiko Okano, Miki Onoue, Masahiro Kiuchi, Chiaki Iwamura, Tomohisa Iinuma, Motoko Y Kimura, Nobuyuki Ebihara, Toyoyuki Hanazawa, Toshinori Nakayama, Kiyoshi Hirahara |
Journal | Pharmacology & therapeutics
(Pharmacol Ther)
Vol. 247
Pg. 108445
(Jul 2023)
ISSN: 1879-016X [Electronic] England |
PMID | 37201737
(Publication Type: Journal Article, Review)
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Copyright | Copyright © 2023 Elsevier Inc. All rights reserved. |
Chemical References |
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Topics |
- Humans
- Cytokines
- Interleukin-5
(therapeutic use)
- Hypersensitivity
(drug therapy)
- Th2 Cells
- Dermatitis, Atopic
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