Mycoplasma pneumoniae and Chlamydia pneumoniae in asthma -: Effect of clarithromycin

被引:256
作者
Kraft, M
Cassell, GH
Pak, J
Martin, RJ
机构
[1] Natl Jewish Med & Res Ctr, Dept Med, Denver, CO 80206 USA
[2] Univ Colorado, Hlth Sci Ctr, Denver, CO 80202 USA
[3] Univ Alabama Birmingham, Dept Microbiol, Birmingham, AL 35294 USA
关键词
airway; asthma; bronchoscopy; chlamydia; mycoplasma;
D O I
10.1378/chest.121.6.1782
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Study objectives: To determine the effect of clarithromycin therapy in patients with asthma. Design: Randomized, double blind, placebo-controlled trial. Setting: A tertiary referral center. Patients or participants: Fifty-five subjects with chronic, stable asthma recruited from the general Denver, CO, community. Interventions: Patients underwent airway evaluation for Mycoplasma pneumoniae and Chlamydia pneumoniae by polymerase chain reaction (PCR) and culture, followed by treatment with clarithromycin, 500 bid, or placebo for 6 weeks. Measurements and results: Outcome variables were lung function, sinusitis as measured by CT, and the inflammatory mediators tumor necrosis factor (TNF)-alpha, interleukin (IL)-2, IL-4, IL-5, and IL-12 messenger RNA (mRNA) measured via in situ hybridization, in airway biopsies, and BAL. Mycoplasma or chlamydia were detected by PCR in 31 of 55 asthmatics. Treatment resulted in a significant improvement in the FEV1, but only in the PCR-positive subjects (2.50 +/- 0.16 to 2.69 +/- 0.19 L, mean SEM; p = 0.05). This was not appreciated in the PCR-negative subjects (2.59 +/- 0.24 to 2.54 +/- 0.18 L, p = 0.85) or the PCR-positive or PCR-negative subjects who received placebo. Sinus CTs revealed no change in sinusitis with clarithromycin treatment. In situ hybridization revealed no significant difference in baseline airway tissue or BAL-mediator expression between the PCR-positive and PCR-negative subjects. However, the PCR-positive subjects who received clarithromycin demonstrated a reduction in TNF-alpha (p = 0.006), IL-5 (p = 0.007), and IL-12 (p = 0.004) mRNA in BAL and TNF-alpha mRNA in airway tissue (p = 0.0009). The PCR-negative subjects who received clarithromycin only demonstrated a reduction in TNF-alpha (p = 0.01) and IL-12 (p = 0.002) mRNA in BAL and TNF-alpha mRNA in airway tissue (p = 0.004). There were no significant differences in cytokine expression in those subjects who received placebo. Conclusions: These observations support the hypothesis that clarithromycin therapy improves lung function, but only in those subjects with positive PCR findings for M pneumoniae or C pneumoniae.
引用
收藏
页码:1782 / 1788
页数:7
相关论文
共 46 条
[1]   ACUTE EXACERBATIONS OF ASTHMA IN ADULTS - ROLE OF CHLAMYDIA-PNEUMONIAE INFECTION [J].
ALLEGRA, L ;
BLASI, F ;
CENTANNI, S ;
COSENTINI, R ;
DENTI, F ;
RACCANELLI, R ;
TARSIA, P ;
VALENTI, V .
EUROPEAN RESPIRATORY JOURNAL, 1994, 7 (12) :2165-2168
[2]  
ALVAREZ J, 1990, Journal of Allergy and Clinical Immunology, V85, P195
[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]  
[Anonymous], 1987, AM REV RESPIR DIS, V136, P225
[5]  
BERKOVICH S, 1970, ANN ALLERGY, V28, P43
[6]  
BLACK PN, 1996, EUR RESPIR REV, V6, P240
[7]   Chlamydia pneumoniae and asthma [J].
Cook, PJ ;
Davies, P ;
Tunnicliffe, W ;
Ayres, JG ;
Honeybourne, D ;
Wise, R .
THORAX, 1998, 53 (04) :254-259
[8]   Chronic Chlamydia pneumoniae infection and asthma exacerbations in children [J].
Cunningham, AF ;
Johnston, SL ;
Julious, SA ;
Lampe, FC ;
Ward, ME .
EUROPEAN RESPIRATORY JOURNAL, 1998, 11 (02) :345-349
[9]   DETECTION OF ANTI-CHLAMYDIA PNEUMONIAE IGE IN CHILDREN WITH REACTIVE AIRWAY DISEASE [J].
EMRE, U ;
SOKOLOVSKAYA, N ;
ROBLIN, PM ;
SCHACHTER, J ;
HAMMERSCHLAG, MR .
JOURNAL OF INFECTIOUS DISEASES, 1995, 172 (01) :265-267
[10]   THE ASSOCIATION OF CHLAMYDIA-PNEUMONIAE INFECTION AND REACTIVE AIRWAY DISEASE IN CHILDREN [J].
EMRE, U ;
ROBLIN, RM ;
GELLING, M ;
DUMORNAY, W ;
RAO, M ;
HAMMERSCHLAG, MR ;
SCHACHTER, J .
ARCHIVES OF PEDIATRICS & ADOLESCENT MEDICINE, 1994, 148 (07) :727-732