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CRTH2 antagonists in asthma: current perspectives

Chemoattractant receptor-homologous molecule expressed on T(H)2 cells (CRTH2) binds to prostaglandin D(2). CRTH2 is expressed on various cell types including eosinophils, mast cells, and basophils. CRTH2 and prostaglandin D(2) are involved in allergic inflammation and eosinophil activation. Orally a...

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Detalles Bibliográficos
Autores principales: Singh, Dave, Ravi, Arjun, Southworth, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5733922/
https://www.ncbi.nlm.nih.gov/pubmed/29276415
http://dx.doi.org/10.2147/CPAA.S119295
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author Singh, Dave
Ravi, Arjun
Southworth, Thomas
author_facet Singh, Dave
Ravi, Arjun
Southworth, Thomas
author_sort Singh, Dave
collection PubMed
description Chemoattractant receptor-homologous molecule expressed on T(H)2 cells (CRTH2) binds to prostaglandin D(2). CRTH2 is expressed on various cell types including eosinophils, mast cells, and basophils. CRTH2 and prostaglandin D(2) are involved in allergic inflammation and eosinophil activation. Orally administered CRTH2 antagonists are in clinical development for the treatment of asthma. The biology and clinical trial data indicate that CRTH2 antagonists should be targeted toward eosinophilic asthma. This article reviews the clinical evidence for CRTH2 involvement in asthma pathophysiology and clinical trials of CRTH2 antagonists in asthma. CRTH2 antagonists could provide a practical alternative to biological treatments for patients with severe asthma. Future perspectives for this class of drug are considered, including the selection of the subgroup of patients most likely to show a meaningful treatment response.
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spelling pubmed-57339222017-12-22 CRTH2 antagonists in asthma: current perspectives Singh, Dave Ravi, Arjun Southworth, Thomas Clin Pharmacol Review Chemoattractant receptor-homologous molecule expressed on T(H)2 cells (CRTH2) binds to prostaglandin D(2). CRTH2 is expressed on various cell types including eosinophils, mast cells, and basophils. CRTH2 and prostaglandin D(2) are involved in allergic inflammation and eosinophil activation. Orally administered CRTH2 antagonists are in clinical development for the treatment of asthma. The biology and clinical trial data indicate that CRTH2 antagonists should be targeted toward eosinophilic asthma. This article reviews the clinical evidence for CRTH2 involvement in asthma pathophysiology and clinical trials of CRTH2 antagonists in asthma. CRTH2 antagonists could provide a practical alternative to biological treatments for patients with severe asthma. Future perspectives for this class of drug are considered, including the selection of the subgroup of patients most likely to show a meaningful treatment response. Dove Medical Press 2017-12-15 /pmc/articles/PMC5733922/ /pubmed/29276415 http://dx.doi.org/10.2147/CPAA.S119295 Text en © 2017 Singh et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Review
Singh, Dave
Ravi, Arjun
Southworth, Thomas
CRTH2 antagonists in asthma: current perspectives
title CRTH2 antagonists in asthma: current perspectives
title_full CRTH2 antagonists in asthma: current perspectives
title_fullStr CRTH2 antagonists in asthma: current perspectives
title_full_unstemmed CRTH2 antagonists in asthma: current perspectives
title_short CRTH2 antagonists in asthma: current perspectives
title_sort crth2 antagonists in asthma: current perspectives
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5733922/
https://www.ncbi.nlm.nih.gov/pubmed/29276415
http://dx.doi.org/10.2147/CPAA.S119295
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