Recent research and developmental strategy of anti-asthma drugs

被引:25
|
作者
Nagai, Hiroichi [1 ]
机构
[1] Gifu Jr Coll Hlth Sci, Gifu 5008281, Japan
关键词
Asthma; Allergic inflammation; Glucocorticoid; Controller; Reliever; Immunomodulator; Lipid mediator; SUPLATAST TOSILATE IPD-1151T; INDUCED AIRWAY HYPERRESPONSIVENESS; EXPERIMENTAL ALLERGIC REACTIONS; THROMBOXANE A(2) RECEPTOR; CYSTEINYL LEUKOTRIENE RECEPTOR; TH2 CYTOKINE INHIBITOR; GUINEA-PIGS; ATOPIC-DERMATITIS; CPG OLIGODEOXYNUCLEOTIDES; ANTIALLERGIC AGENT;
D O I
10.1016/j.pharmthera.2011.09.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Extensive research over the past decade has provided information about the pharmacotherapy of bronchial asthma (BA). Anti-asthma drugs are classified into two categories: relievers (for the relief of asthma attack symptoms) and controllers (for the prevention of asthma symptoms). This paper aims to review the recent advancements of anti-asthma drugs that are controller medicines. The controllers mainly act on immune and inflammatory responses in BA development. 1) Immunomodulators. Drugs that act on the immune response are classified into two categories: immuno-suppressors and immunomodulators, including immunopotentiators. The immunomodulation of the Th1 and Th2 imbalance is the first strategy of the controller because allergic BA is thought to be caused by Th2-polarized immunity. Suplatast is a novel immunomodulator that can adjust the imbalance in the Th1/Th2 immune response and shows clear clinical efficacy against BA. The immunomodulator approach has shifted from a more theoretical and conceptual model to one supported by evidence of clinical efficacy. 2) Anti-inflammatory agents. Corticosteroids, mast cell stabilizers and autacoid inhibitors are anti-inflammatory agents for BA. The clinical superiority of the combined therapy of inhaled corticosteroids and long-acting beta2 agonists is evident. This combined therapy shows a potent synergic anti-inflammatory effect compared to the effect by corticosteroids alone. Currently, the anti-inflammatory agents for BA under development are drugs affecting lipid mediators. The prostaglandin (PG) D2 antagonist, PGE2, EP3 agonist and PGI2 agonist are being considered in addition to well-established leukotriene and thromboxane A2 inhibitors. New development strategies and therapeutics for controllers are described in this review. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:70 / 78
页数:9
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