New targets for drug development in asthma

被引:186
作者
Adcock, Ian M. [1 ,2 ]
Caramori, Gaetano [3 ]
Chung, K. Fan [1 ,2 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Airways Dis Sect, Natl Heart & Lung Inst, London SW3 6LY, England
[2] Kings & Imperial Coll, MRC Asthma UK Ctr Allerg Mech Asthma, London, ON, Canada
[3] Univ Ferrara, Ctr Res Asthma & COPD, I-44100 Ferrara, Italy
基金
英国惠康基金; 英国医学研究理事会;
关键词
D O I
10.1016/S0140-6736(08)61449-X
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Asthma is a chronic inflammatory disease that affects about 300 million people worldwide, a total that is expected to rise to about 400 million over the next 15-20 years. Most asthmatic individuals respond well to the currently available treatments of inhaled corticosteroids and beta-adrenergic agonists; however, 5-10% have severe disease that responds poorly. Improved knowledge of asthma mechanisms has led to the recognition of different asthma phenotypes that might reflect distinct types of inflammation, explaining the effectiveness of anti-leucotrienes and the anti-IgE monoclonal antibody omalizumab in some patients. However, more knowledge of the inflammatory mechanisms within the airways is required. Improvements in available therapies-such as the development of fast-onset, once-a-day combination drugs with better safety profiles-will occur. Other drugs, such as inhaled p38 MAPK inhibitors and anti-oxidants, that target specific pathways or mediators could prove useful as monotherapies, but could also, in combination with corticosteroids, reduce the corticosteroid insensitivity often seen in severe asthma. Biological agents directed against the interleukin-13 pathway and new immunoregulatory agents that modulate functions of T-regulatory and T-helper-17 cells are likely to be successful. Patient-specific treatments will depend on the development of discriminatory handprints of distinct asthma subtypes and are probably over the horizon. Although a cure is unlikely to be developed in the near future, a greater understanding of disease mechanisms could bring such a situation nearer to reality.
引用
收藏
页码:1073 / 1087
页数:15
相关论文
共 142 条
  • [21] Effects of recombinant human interleukin-12 on eosinophils, airway hyper-responsiveness, and the late asthmatic response
    Bryan, SA
    O'Connor, BJ
    Matti, S
    Leckie, MJ
    Kanabar, V
    Khan, J
    Warrington, SJ
    Renzetti, L
    Rames, A
    Bock, JA
    Boyce, MJ
    Hansel, TT
    Holgate, ST
    Barnes, PJ
    [J]. LANCET, 2000, 356 (9248) : 2149 - 2153
  • [22] Bundschuh DS, 2001, J PHARMACOL EXP THER, V297, P280
  • [23] Expression of GATA family of transcription factors in T-cells, monocytes and bronchial biopsies
    Caramori, G
    Lim, S
    Ito, K
    Tomita, K
    Oates, T
    Jazrawi, E
    Chung, KF
    Barnes, PJ
    Adcock, IM
    [J]. EUROPEAN RESPIRATORY JOURNAL, 2001, 18 (03) : 466 - 473
  • [24] New drugs targeting Th2 lymphocytes in asthma
    Gaetano Caramori
    David Groneberg
    Kazuhiro Ito
    Paolo Casolari
    Ian M Adcock
    Alberto Papi
    [J]. Journal of Occupational Medicine and Toxicology, 3 (Suppl 1)
  • [25] T-cell effector pathways in allergic diseases: Transcriptional mechanisms and therapeutic targets
    Chatila, Talal A.
    Li, Ning
    Garcia-Llore, Maria
    Kim, Hyon-Jeen
    Nel, Andre E.
    [J]. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2008, 121 (04) : 812 - 823
  • [26] Chung K Fan, 2004, Treat Respir Med, V3, P279, DOI 10.2165/00151829-200403050-00002
  • [27] Phosphodiesterase inhibitors in airways disease
    Chung, KF
    [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 2006, 533 (1-3) : 110 - 117
  • [28] Chung KF, 1999, EUR RESPIR J, V13, P1198
  • [29] Epithelial cell proliferation contributes to airway remodelina in severe asthma
    Cohen, Lance
    Xueping, E.
    Tarsi, Jaime
    Ramkumar, Thiruvamoor
    Horiuchi, Todd K.
    Cochran, Rebecca
    DeMartino, Steve
    Schechtman, Kenneth B.
    Hussain, Iftikhar
    Holtzman, Michael J.
    Castro, Mario
    [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2007, 176 (02) : 138 - 145
  • [30] Histone acetylase and deacetylase activity in alveolar macrophages and blood mononocytes in asthma
    Cosío, BG
    Mann, B
    Ito, K
    Jazrawi, E
    Barnes, PJ
    Chung, KF
    Adcock, IM
    [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2004, 170 (02) : 141 - 147