Macrolide and occult infection in asthma

被引:20
作者
Cazzola, M
Matera, MG
Blasi, F
机构
[1] A Cardarelli Hosp, Dept Resp Med, Unit Pneumol & Allergol, Naples, Italy
[2] Univ Naples 2, Sch Med, Dept Expt Med, Unit Pharmacol, Naples, Italy
[3] Univ Milan, Inst Care & Res, Polyclin Hosp, Inst Resp Med, Milan, Italy
关键词
atypical pathogens; occult infection; asthma; macrolide;
D O I
10.1097/00063198-200401000-00003
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Purpose of review A small percentage of asthma exacerbations are linked with infection by an atypical bacterium, such as Chlamydia pneumoniae or Mycoplasma pneumoniae. These bacteria also have been proposed to cause occult chronic lower airway inflammation and to initiate nonatopic asthma in adults. Consequently, the logical procedure would be to eliminate these pathogens as soon and as thoroughly as possible using antibiotics. Nonetheless, antibiotics are not recommended even for the treatment of acute asthma exacerbations except as needed for comorbid conditions. These discrepancies highlight the need to define the role, if any, of antimicrobials that are active against atypical pathogens, mainly macrolides, but also tetracyclines and fluoroquinolones, in the treatment of asthma. Recent findings Macrolides are antibiotics with both antimicrobial and anti inflammatory activities. Some studies have documented that these agents could be useful in the treatment of occult infection in asthma because of their antimicrobial activity against atypical pathogens. They could also lead to reduction of the airways inflammation by decreasing the transcription of mRNA for a variety of cytokines and inhibiting interleukin-8 release by eosinophils, and therefore improvement of symptoms and pulmonary function. These effects are not caused by bronchodilation, elevation of serum theophylline level, or steroid-sparing mechanism. Summary The available clinical evidence seems to support use of macrolides in the treatment of asthma because of their antimicrobial activity. However, studies that may confirm this hypothesis are scarce and with limited scientific value because of their open, uncontrolled design.
引用
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页码:7 / 14
页数:8
相关论文
共 71 条
[1]   Interleukin-8 gene repression by clarithromycin is mediated by the activator protein-1 binding site in human bronchial epithelial cells [J].
Abe, S ;
Nakamura, H ;
Inoue, S ;
Takeda, H ;
Saito, H ;
Kato, S ;
Mukaida, N ;
Matsushima, K ;
Tomoike, H .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2000, 22 (01) :51-60
[2]   Eosinophil apoptosis caused by theophylline, glucocorticoids, and macrolides after stimulation with IL-5 [J].
Adachi, T ;
Motojima, S ;
Hirata, A ;
Fukuda, T ;
Kihara, N ;
Kosaku, A ;
Ohtake, H ;
Makino, S .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1996, 98 (06) :S207-S215
[3]   Clarithromycin suppresses bronchial hyperresponsiveness associated with eosinophilic inflammation in patients with asthma [J].
Amayasu, H ;
Yoshida, S ;
Ebana, S ;
Yamamoto, Y ;
Nishikawa, T ;
Shoji, T ;
Nakagawa, H ;
Hasegawa, H ;
Nakabayashi, M ;
Ishizaki, Y .
ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY, 2000, 84 (06) :594-598
[4]  
ANDRADE WP, 1983, ANN ALLERGY, V51, P515
[5]   Seroprevalence of chronic Chlamydia pneumoniae infection in patients affected by chronic stable asthma [J].
Barbaro, MPF ;
Resta, O ;
Aliani, M ;
Guido, P ;
Izzo, C ;
Logroscino, C ;
Epifani, V ;
Bisconti, M ;
Gerardi, R ;
Del Prete, R ;
Miragliotta, G .
CLINICAL MICROBIOLOGY AND INFECTION, 2002, 8 (06) :358-362
[6]   Transcription factors and asthma [J].
Barnes, PJ ;
Adcock, IM .
EUROPEAN RESPIRATORY JOURNAL, 1998, 12 (01) :221-234
[7]   A SOLUBLE 60-KILODALTON ANTIGEN OF CHLAMYDIA-SPP IS A HOMOLOG OF ESCHERICHIA-COLI GROEL [J].
BAVOIL, P ;
STEPHENS, RS ;
FALKOW, S .
MOLECULAR MICROBIOLOGY, 1990, 4 (03) :461-469
[8]   Anti-Chlamydia pneumoniae heat shock protein 10 antibodies in asthmatic adults [J].
Betsou, F ;
Sueur, JM ;
Orfila, J .
FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY, 2003, 35 (02) :107-111
[9]   Trial of roxithromycin in subjects with asthma and serological evidence of infection with Chlamydia pneumoniae [J].
Black, PN ;
Blasi, F ;
Jenkins, CR ;
Scicchitano, R ;
Mills, GD ;
Rubinfeld, AR ;
Ruffin, RE ;
Mullins, PR ;
Dangain, J ;
Cooper, BC ;
David, DB ;
Allegra, L .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2001, 164 (04) :536-541
[10]  
Blasi F, 2001, Monaldi Arch Chest Dis, V56, P276