Gene therapy strategies for asthma

被引:20
作者
Demoly, P [1 ]
Mathieu, M [1 ]
Curiel, DT [1 ]
Godard, P [1 ]
Bousquet, J [1 ]
Michel, FB [1 ]
机构
[1] UNIV ALABAMA, GENE THERAPY PROGRAM, BIRMINGHAM, AL USA
关键词
asthma; gene therapy; bronchial epithelium; inflammation; lymphocytes; adhesion molecules; cytokines;
D O I
10.1038/sj.gt.3300419
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Asthma is a disease which is increasing in frequency and severity despite the incontestable advances in the understanding of its physiology and treatment. New therapeutic strategies are therefore required and at the time when a new treatment, that of gene therapy, is giving hope for the treatment of so far incurable illnesses, it would seem to us to be useful to discuss the possible use of this treatment in severe asthma and in particular in the case of the most severe asthmatic patients requiring continuous oral steroid treatment (referred to as steroid-dependent). These patients are those who require particular medical attention, a they often need to be admitted to hospital and they represent over 50% of the fetal costs associated with asthma. No satisfactory alternative therapy is currently available. in this regard, a variety of gene-based strategies have recently-been proposed for inflammatory and immunologic disorders. It is thus the purpose of this review to consider ifs application to asthma therapy although there are very few published works that directly bear on gene therapy linked to asthma. After a brief outline of the epidemiology of asthma, its genetics and the available animal models, we will focus on its immunopathology slanting the discussion towards the possibility of a gene-based treatment.
引用
收藏
页码:507 / 516
页数:10
相关论文
共 95 条
[1]   ALPHA(4)-INTEGRINS MEDIATE ANTIGEN-INDUCED LATE BRONCHIAL RESPONSES AND PROLONGED AIRWAY HYPERRESPONSIVENESS IN SHEEP [J].
ABRAHAM, WM ;
SIELCZAK, MW ;
AHMED, A ;
CORTES, A ;
LAUREDO, IT ;
KIM, J ;
PEPINSKY, B ;
BENJAMIN, CD ;
LEONE, DR ;
LOBB, RR ;
WELLER, PF .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 93 (02) :776-787
[2]   ABNORMAL GLUCOCORTICOID RECEPTOR ACTIVATOR PROTEIN-1 INTERACTION IN STEROID-RESISTANT ASTHMA [J].
ADCOCK, IM ;
LANE, SJ ;
BROWN, CR ;
LEE, TH ;
BARNES, PJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 182 (06) :1951-1958
[3]  
ADCOCK IM, 1995, J IMMUNOL, V154, P3500
[4]   STEROID-RESISTANT ASTHMA - IMMUNOLOGICAL AND PHARMACOLOGICAL FEATURES [J].
ALVAREZ, J ;
SURS, W ;
LEUNG, DYM ;
IKLE, D ;
GELFAND, EW ;
SZEFLER, SJ .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1992, 89 (03) :714-721
[5]  
ARRIGHI HM, 1995, ANN ALLERG ASTHMA IM, V74, P321
[6]   AN INTERLEUKIN-4 (IL-4) MUTANT PROTEIN INHIBITS BOTH IL-4 OR IL-13-INDUCED HUMAN IMMUNOGLOBULIN-G4 (IGG4) AND IGE SYNTHESIS AND B-CELL PROLIFERATION - SUPPORT FOR A COMMON COMPONENT SHARED BY IL-4 AND IL-13 RECEPTORS [J].
AVERSA, G ;
PUNNONEN, J ;
COCKS, BG ;
MALEFYT, RD ;
VEGA, F ;
ZURAWSKI, SM ;
ZURAWSKI, G ;
DEVRIES, JE .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 178 (06) :2213-2218
[7]   GLUCOCORTICOID RESISTANCE IN ASTHMA [J].
BARNES, PJ ;
GREENING, AP ;
CROMPTON, GK .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1995, 152 (06) :S125-S140
[8]   Lung inflammation and epithelial changes in a murine model of atopic asthma [J].
Blyth, DI ;
Pedrick, MS ;
Savage, TJ ;
Hessel, EM ;
Fattah, D .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1996, 14 (05) :425-438
[9]   RECOMBINANT GAMMA INTERFERON IN TREATMENT OF PATIENTS WITH ATOPIC-DERMATITIS AND ELEVATED IGE LEVELS [J].
BOGUNIEWICZ, M ;
JAFFE, HS ;
IZU, A ;
SULLIVAN, MJ ;
YORK, D ;
GEHA, RS ;
LEUNG, DYM .
AMERICAN JOURNAL OF MEDICINE, 1990, 88 (04) :365-370
[10]  
BOGUNIEWICZ M, 1993, J ALLERGY CLIN IMMUN, V91, P226