Drug-induced mast cell eradication: A novel approach to treat mast cell activation disorders?
KIT
Mast cell activation syndrome
Mast cells
avapritinib
midostaurin
tyrosine kinase inhibitor
Journal
The Journal of allergy and clinical immunology
ISSN: 1097-6825
Titre abrégé: J Allergy Clin Immunol
Pays: United States
ID NLM: 1275002
Informations de publication
Date de publication:
06 2022
06 2022
Historique:
received:
17
02
2022
revised:
28
03
2022
accepted:
06
04
2022
pubmed:
15
4
2022
medline:
9
6
2022
entrez:
14
4
2022
Statut:
ppublish
Résumé
Mast cell (MC) activation is a key event in allergic reactions, other inflammatory states, and MC activation syndromes. MC-stabilizing agents, mediator-targeting drugs, and drugs interfering with mediator effects are often prescribed for these patients. However, the clinical efficacy of these drugs varies depending on the numbers of involved MCs and the underlying pathology. One straightforward approach would be to eradicate the primary target cell. To date however, no MC-eradicating treatment approach has been developed for patients with MC activation disorders. Nevertheless, recent data suggest that long-term treatment with agents effectively inhibiting KIT function results in the virtual eradication of tissue MCs and a sustained decrease in serum tryptase levels. In many of these patients, MC depletion is associated with a substantial improvement in mediator-induced symptoms. In patients with an underlying KIT D816V-positive mastocytosis, such MC eradication requires an effective inhibitor of KIT D816V, such as avapritinib. However, the use of KIT inhibitors must be balanced against their potential side effects. Here we discuss MC-eradicating strategies in various disease models, the feasibility of this approach, available clinical data, and future prospects for the use of KIT-targeting drugs in MC activation disorders.
Identifiants
pubmed: 35421448
pii: S0091-6749(22)00451-1
doi: 10.1016/j.jaci.2022.04.003
pii:
doi:
Substances chimiques
Proto-Oncogene Proteins c-kit
EC 2.7.10.1
Staurosporine
H88EPA0A3N
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1866-1874Informations de copyright
Copyright © 2022 The Authors. Published by Elsevier Inc. All rights reserved.