Immunologic Therapeutic Interventions in Asthma Impact on Natural History

被引:6
作者
Bourdin, Arnaud [1 ,2 ]
Humbert, Marc [3 ]
Chanez, Pascal [4 ]
机构
[1] CHU Montpellier, Serv Malad Resp, Hop Arnaud de Villeneuve, Dept Resp Dis, Montpellier, France
[2] Univ Montpellier 1 & 2, CHU Arnaud de Villeneuve, INSERM, Physiol & Med Expt Coeur & Muscles U1046, Montpellier, France
[3] Univ Paris 11, Hop Antoine Beclere, Assistance Publ Hop Paris,INSERM,U999, Serv Pneumol & Reanimat Resp,Ctr Natl Reference H, F-92140 Clamart, France
[4] Aix Marseille Univ, Dept Malad Resp, AP HM, Lab Immunol,CNRS,INSERM,U1067,UMR7733, Marseille, France
关键词
Asthma; Immunology; Therapeutic intervention; PLACEBO-CONTROLLED TRIAL; NECROSIS-FACTOR-ALPHA; IL-5; MESSENGER-RNA; CORTICOSTEROID-DEPENDENT ASTHMA; THYMIC STROMAL LYMPHOPOIETIN; SEVERE PERSISTENT ASTHMA; GENOME-WIDE ASSOCIATION; CD8(+) T-CELLS; AIRWAY INFLAMMATION; MAST-CELLS;
D O I
10.1016/j.ccm.2012.06.004
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
100201 [内科学];
摘要
The discovery of new pathobiological pathways involved in asthma chronicity and reliefs offers novel therapeutic avenues. Enhanced phenotyping criteria associated with simple biologic characterization allowed to test targeted interventions in selected patients. Long-term studies are de facto lacking but required to address their impact on the natural history of the disease. Here, the authors review all potential available therapeutics based on immunologic pathways involved in asthma pathophysiology during the last decade.
引用
收藏
页码:585 / +
页数:14
相关论文
共 139 条
[1]
ALEXANDER AG, 1995, EUR RESPIR J, V8, P574
[2]
TRIAL OF CYCLOSPORINE IN CORTICOSTEROID-DEPENDENT CHRONIC SEVERE ASTHMA [J].
ALEXANDER, AG ;
BARNES, NC ;
KAY, AB .
LANCET, 1992, 339 (8789) :324-328
[3]
Multitargeted approach using antisense oligonucleotides for the treatment of asthma [J].
Allakhverdi, Z. ;
Allam, M. ;
Guimond, A. ;
Ferrari, N. ;
Zemzoumi, K. ;
Seguin, R. ;
Paquet, L. ;
Renzi, P. M. .
OLIGONUCLEOTIDE THERAPEUTICS, 2006, 1082 :62-73
[4]
Thymic stfomal lymphopoietin is released by human epithelial cells in response to microbes, trauma, or inflammation and potently activates mast cells [J].
Allakhverdi, Zoulfia ;
Comeau, Michael R. ;
Jessup, Heidi K. ;
Yoon, Bo-Rin Park ;
Brewer, Avery ;
Chartier, Suzanne ;
Paquette, Nicole ;
Ziegler, Steven F. ;
Sarfati, Marika ;
Delespesse, Guy .
JOURNAL OF EXPERIMENTAL MEDICINE, 2007, 204 (02) :253-258
[5]
Antoniu SA, 2010, CURR OPIN MOL THER, V12, P233
[6]
IgE expression pattern in lung: Relation to systemic IgE and asthma phenotypes [J].
Balzar, Silvana ;
Strand, Matthew ;
Rhodes, Diane ;
Wenzel, Sally E. .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2007, 119 (04) :855-862
[7]
[8]
Stability of asthma control with regular treatment: an analysis of the Gaining Optimal Asthma controL (GOAL) study [J].
Bateman, E. D. ;
Bousquet, J. ;
Busse, W. W. ;
Clark, T. J. H. ;
Gul, N. ;
Gibbs, M. ;
Pedersen, S. .
ALLERGY, 2008, 63 (07) :932-938
[9]
Can guideline-defined asthma control be achieved? The gaining optimal asthma control study [J].
Bateman, ED ;
Boushey, HA ;
Bousquet, J ;
Busse, WW ;
Clark, TJH ;
Pauwels, RA ;
Pedersen, SE .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2004, 170 (08) :836-844
[10]
Diagnosis and definition of severe refractory asthma: an international consensus statement from the Innovative Medicine Initiative (IMI) [J].
Bel, Elisabeth H. ;
Sousa, Ana ;
Fleming, Louise ;
Bush, Andrew ;
Chung, K. Fan ;
Versnel, Jennifer ;
Wagener, Ariane H. ;
Wagers, Scott S. ;
Sterk, Peter J. ;
Compton, Chris H. .
THORAX, 2011, 66 (10) :910-917