Abstract
Asthma is a chronic airway disease resulting from inappropriate Th2-cell biased activation. Interleukin (IL)-4, IL-5 and IL-13 produced by Th2 cells contribute to the inflammatory process. Attempts for inhibiting interleukin-4 or IL- 5 gave disappointing results. The simultaneous inhibition of several Th2-cytokines could be a more promising issue. Several arguments support the concept that Th2-cells express selective markers that could be targeted in asthma. Our group showed that Th2-cells selectively up-regulated dihydropyridine-sensitive Ca2+ (DHP-Ca) channels essential for Ca2+ signaling and type-2 cytokine production. Indeed, DHP-Ca antagonist effectively prevented or even reverted airway inflammation, airway remodeling and airway hyperresponsiveness in experimental models of asthma. Although it remains to be formally demonstrated that human lung infiltrating T-lymphocytes in asthmatic patients express DHP- Ca2+ channels, we hypothesize that targeting DHP-Ca channels in T-lymphocytes could represent an efficient strategy in the treatment of asthma.This review article also discussed patents relevant to the field.
Keywords: Asthma, dihydropyridine receptors or dihydropyridine-sensitive Ca2+ channels, airway hyperresponsiveness, calcium signaling, Th2-lymphocytes, interleukins 4, 5 and 13
Recent Patents on Inflammation & Allergy Drug Discovery
Title: Dihydropyridine Receptor Blockade in the Treatment of Asthma
Volume: 2 Issue: 2
Author(s): Lucette Pelletier and Jean-Charles Guery
Affiliation:
Keywords: Asthma, dihydropyridine receptors or dihydropyridine-sensitive Ca2+ channels, airway hyperresponsiveness, calcium signaling, Th2-lymphocytes, interleukins 4, 5 and 13
Abstract: Asthma is a chronic airway disease resulting from inappropriate Th2-cell biased activation. Interleukin (IL)-4, IL-5 and IL-13 produced by Th2 cells contribute to the inflammatory process. Attempts for inhibiting interleukin-4 or IL- 5 gave disappointing results. The simultaneous inhibition of several Th2-cytokines could be a more promising issue. Several arguments support the concept that Th2-cells express selective markers that could be targeted in asthma. Our group showed that Th2-cells selectively up-regulated dihydropyridine-sensitive Ca2+ (DHP-Ca) channels essential for Ca2+ signaling and type-2 cytokine production. Indeed, DHP-Ca antagonist effectively prevented or even reverted airway inflammation, airway remodeling and airway hyperresponsiveness in experimental models of asthma. Although it remains to be formally demonstrated that human lung infiltrating T-lymphocytes in asthmatic patients express DHP- Ca2+ channels, we hypothesize that targeting DHP-Ca channels in T-lymphocytes could represent an efficient strategy in the treatment of asthma.This review article also discussed patents relevant to the field.
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Cite this article as:
Pelletier Lucette and Guery Jean-Charles, Dihydropyridine Receptor Blockade in the Treatment of Asthma, Recent Patents on Inflammation & Allergy Drug Discovery 2008; 2 (2) . https://dx.doi.org/10.2174/187221308784543638
DOI https://dx.doi.org/10.2174/187221308784543638 |
Print ISSN 1872-213X |
Publisher Name Bentham Science Publisher |
Online ISSN 2212-2710 |
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