Effect of 6 Months of Erythromycin Treatment on Inflammatory Cells in Induced Sputum and Exacerbations in Chronic Obstructive Pulmonary Disease

Background: Chronic obstructive pulmonary disease (COPD) is characterized by airway inflammation and is associated with acute exacerbations. Macrolide antibiotics have been shown to exhibit anti-inflammatory effects in some chronic airway inflammatory diseases. Objective: The aim of this study was t...

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Published inRespiration Vol. 80; no. 6; pp. 445 - 452
Main Authors He, Zhi-Yi, Ou, Li-Mei, Zhang, Jian-Quan, Bai, Jing, Liu, Guang-Nan, Li, Mei-Hua, Deng, Jing-Min, MacNee, William, Zhong, Xiao-Ning
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Published Basel, Switzerland Karger 01.01.2010
S. Karger AG
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Abstract Background: Chronic obstructive pulmonary disease (COPD) is characterized by airway inflammation and is associated with acute exacerbations. Macrolide antibiotics have been shown to exhibit anti-inflammatory effects in some chronic airway inflammatory diseases. Objective: The aim of this study was to assess the effect of treatment with erythromycin on airway inflammation and health outcome in COPD patients. Methods: We conducted a randomized, placebo-controlled, double-blind trial of erythromycin for a period of 6 months. Thirty-six COPD patients were randomized to treatment with oral erythromycin (125 mg, three times/day) or placebo. The primary outcomes were neutrophil number in sputum and exacerbations. Results: Thirty-one patients completed the study. At the end of treatment, neutrophil counts in the sputum were significantly decreased in the group treated with erythromycin compared with placebo-treated patients (p = 0.005). Total cells in the sputum and neutrophil elastase in sputum supernatant were also significantly decreased in those treated with erythromycin compared with the placebo group (p = 0.021 and p = 0.024, respectively). The mean exacerbation rate was lower in the erythromycin group than in the placebo group (relative risk = 0.554, p = 0.042). Kaplan-Meier survival analysis showed that erythromycin significantly delayed the time to the first COPD exacerbation compared with placebo (p = 0.032). Conclusions: Erythromycin treatment in COPD patients can reduce airway inflammation and decrease exacerbations and may therefore be useful in the management of COPD.
AbstractList Chronic obstructive pulmonary disease (COPD) is characterized by airway inflammation and is associated with acute exacerbations. Macrolide antibiotics have been shown to exhibit anti-inflammatory effects in some chronic airway inflammatory diseases.BACKGROUNDChronic obstructive pulmonary disease (COPD) is characterized by airway inflammation and is associated with acute exacerbations. Macrolide antibiotics have been shown to exhibit anti-inflammatory effects in some chronic airway inflammatory diseases.The aim of this study was to assess the effect of treatment with erythromycin on airway inflammation and health outcome in COPD patients.OBJECTIVEThe aim of this study was to assess the effect of treatment with erythromycin on airway inflammation and health outcome in COPD patients.We conducted a randomized, placebo-controlled, double-blind trial of erythromycin for a period of 6 months. Thirty-six COPD patients were randomized to treatment with oral erythromycin (125 mg, three times/day) or placebo. The primary outcomes were neutrophil number in sputum and exacerbations.METHODSWe conducted a randomized, placebo-controlled, double-blind trial of erythromycin for a period of 6 months. Thirty-six COPD patients were randomized to treatment with oral erythromycin (125 mg, three times/day) or placebo. The primary outcomes were neutrophil number in sputum and exacerbations.Thirty-one patients completed the study. At the end of treatment, neutrophil counts in the sputum were significantly decreased in the group treated with erythromycin compared with placebo-treated patients (p = 0.005). Total cells in the sputum and neutrophil elastase in sputum supernatant were also significantly decreased in those treated with erythromycin compared with the placebo group (p = 0.021 and p = 0.024, respectively). The mean exacerbation rate was lower in the erythromycin group than in the placebo group (relative risk = 0.554, p = 0.042). Kaplan-Meier survival analysis showed that erythromycin significantly delayed the time to the first COPD exacerbation compared with placebo (p = 0.032).RESULTSThirty-one patients completed the study. At the end of treatment, neutrophil counts in the sputum were significantly decreased in the group treated with erythromycin compared with placebo-treated patients (p = 0.005). Total cells in the sputum and neutrophil elastase in sputum supernatant were also significantly decreased in those treated with erythromycin compared with the placebo group (p = 0.021 and p = 0.024, respectively). The mean exacerbation rate was lower in the erythromycin group than in the placebo group (relative risk = 0.554, p = 0.042). Kaplan-Meier survival analysis showed that erythromycin significantly delayed the time to the first COPD exacerbation compared with placebo (p = 0.032).Erythromycin treatment in COPD patients can reduce airway inflammation and decrease exacerbations and may therefore be useful in the management of COPD.CONCLUSIONSErythromycin treatment in COPD patients can reduce airway inflammation and decrease exacerbations and may therefore be useful in the management of COPD.
Background: Chronic obstructive pulmonary disease (COPD) is characterized by airway inflammation and is associated with acute exacerbations. Macrolide antibiotics have been shown to exhibit anti-inflammatory effects in some chronic airway inflammatory diseases. Objective: The aim of this study was to assess the effect of treatment with erythromycin on airway inflammation and health outcome in COPD patients. Methods: We conducted a randomized, placebo-controlled, double-blind trial of erythromycin for a period of 6 months. Thirty-six COPD patients were randomized to treatment with oral erythromycin (125 mg, three times/day) or placebo. The primary outcomes were neutrophil number in sputum and exacerbations. Results: Thirty-one patients completed the study. At the end of treatment, neutrophil counts in the sputum were significantly decreased in the group treated with erythromycin compared with placebo-treated patients (p = 0.005). Total cells in the sputum and neutrophil elastase in sputum supernatant were also significantly decreased in those treated with erythromycin compared with the placebo group (p = 0.021 and p = 0.024, respectively). The mean exacerbation rate was lower in the erythromycin group than in the placebo group (relative risk = 0.554, p = 0.042). Kaplan-Meier survival analysis showed that erythromycin significantly delayed the time to the first COPD exacerbation compared with placebo (p = 0.032). Conclusions: Erythromycin treatment in COPD patients can reduce airway inflammation and decrease exacerbations and may therefore be useful in the management of COPD. [PUBLICATION ABSTRACT]
Background: Chronic obstructive pulmonary disease (COPD) is characterized by airway inflammation and is associated with acute exacerbations. Macrolide antibiotics have been shown to exhibit anti-inflammatory effects in some chronic airway inflammatory diseases. Objective: The aim of this study was to assess the effect of treatment with erythromycin on airway inflammation and health outcome in COPD patients. Methods: We conducted a randomized, placebo-controlled, double-blind trial of erythromycin for a period of 6 months. Thirty-six COPD patients were randomized to treatment with oral erythromycin (125 mg, three times/day) or placebo. The primary outcomes were neutrophil number in sputum and exacerbations. Results: Thirty-one patients completed the study. At the end of treatment, neutrophil counts in the sputum were significantly decreased in the group treated with erythromycin compared with placebo-treated patients (p = 0.005). Total cells in the sputum and neutrophil elastase in sputum supernatant were also significantly decreased in those treated with erythromycin compared with the placebo group (p = 0.021 and p = 0.024, respectively). The mean exacerbation rate was lower in the erythromycin group than in the placebo group (relative risk = 0.554, p = 0.042). Kaplan-Meier survival analysis showed that erythromycin significantly delayed the time to the first COPD exacerbation compared with placebo (p = 0.032). Conclusions: Erythromycin treatment in COPD patients can reduce airway inflammation and decrease exacerbations and may therefore be useful in the management of COPD.
Chronic obstructive pulmonary disease (COPD) is characterized by airway inflammation and is associated with acute exacerbations. Macrolide antibiotics have been shown to exhibit anti-inflammatory effects in some chronic airway inflammatory diseases. The aim of this study was to assess the effect of treatment with erythromycin on airway inflammation and health outcome in COPD patients. We conducted a randomized, placebo-controlled, double-blind trial of erythromycin for a period of 6 months. Thirty-six COPD patients were randomized to treatment with oral erythromycin (125 mg, three times/day) or placebo. The primary outcomes were neutrophil number in sputum and exacerbations. Thirty-one patients completed the study. At the end of treatment, neutrophil counts in the sputum were significantly decreased in the group treated with erythromycin compared with placebo-treated patients (p = 0.005). Total cells in the sputum and neutrophil elastase in sputum supernatant were also significantly decreased in those treated with erythromycin compared with the placebo group (p = 0.021 and p = 0.024, respectively). The mean exacerbation rate was lower in the erythromycin group than in the placebo group (relative risk = 0.554, p = 0.042). Kaplan-Meier survival analysis showed that erythromycin significantly delayed the time to the first COPD exacerbation compared with placebo (p = 0.032). Erythromycin treatment in COPD patients can reduce airway inflammation and decrease exacerbations and may therefore be useful in the management of COPD.
Author MacNee, William
Ou, Li-Mei
He, Zhi-Yi
Li, Mei-Hua
Bai, Jing
Liu, Guang-Nan
Deng, Jing-Min
Zhong, Xiao-Ning
Zhang, Jian-Quan
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Issue 6
Keywords Exacerbation, respiratory
Chronic obstructive pulmonary disease
Airway inflammation
Anti-inflammatory effects
Macrolides
Neutrophils
Lung disease
Respiratory disease
Antiinflammatory agent
Granulocyte
Inflammation
Erythromycin
Macrolide
Antibiotic
Treatment
Sputum
Bronchus disease
Inflammatory cell
Neutrophil
Antibacterial agent
Pneumology
Language English
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References Keatings VM, Barnes PJ: Granulocyte activation markers in induced sputum: comparison between chronic obstructive pulmonary disease, asthma, and normal subjects. Am J Respir Crit Care Med 1997;155:449–453.9032177
Sant’Anna CA, Stelmach R, Zanetti Feltrin MI, Filho WJ, Chiba T, Cukier A: Evaluation of health-related quality of life in low-income patients with COPD receiving long-term oxygen therapy. Chest 2003;123:136–141.1252761410.1378%2Fchest.123.1.136
Sethi S, Murphy TF: Infection in the pathogenesis and course of chronic obstructive pulmonary disease. N Engl J Med 2008;359:2355–2365.1903888110.1056%2FNEJMra0800353
Giamarellos-Bourboulis EJ: Macrolides beyond the conventional antimicrobials: a class of potent immunomodulators. Int J Antimicrob Agents 2008;31:12–20.1793594910.1016%2Fj.ijantimicag.2007.08.001
Banerjee D, Honeybourne D, Khair OA: The effect of oral clarithromycin on bronchial airway inflammation in moderate-to-severe stable COPD: a randomized controlled trial. Treat Respir Med 2004;3:59–65.1517489410.2165%2F00151829-200403010-00007
Rabe KF, Hurd S, Anzueto A, Barnes PJ, Buist SA, Calverley P, et al: Global strategy for the diagnosis, management, and prevention of chronic obstructive pulmonary disease: GOLD executive summary. Am J Respir Crit Care Med 2007;176:532–555.1750754510.1164%2Frccm.200703-456SO
Culić O, Eraković V, Cepelak I, Barisić K, Brajsa K, Ferencić Z, et al: Azithromycin modulates neutrophil function and circulating inflammatory mediators in healthy human subjects. Eur J Pharmacol 2002;450:277–289.1220832110.1016%2FS0014-2999%2802%2902042-3
Azuma A, Kudoh S: Diffuse panbronchiolitis in East Asia. Respirology 2006;11:249–261.1663508210.1111%2Fj.1440-1843.2006.00845.x
Oishi K, Sonoda F, Kobayashi S, Iwagaki A, Nagatake T, Matsushima K, et al: Role of interleukin-8 (IL-8) and an inhibitory effect of erythromycin on IL-8 release in the airways of patients with chronic airway diseases. Infect Immun 1994;62:4145–4152.7927669
Saraiva-Romanholo BM, Barnabé V, Carvalho AL, Martins MA, Saldiva PH, Nunes Mdo P: Comparison of three methods for differential cell count in induced sputum. Chest 2003;124:1060–1066.1297003810.1378%2Fchest.124.3.1060
He Z, Li B, Yu L, Liu Q, Zhong N, Ran P: Suppression of oxidant-induced glutathione synthesis by erythromycin in human bronchial epithelial cells. Respiration 2008;75:202–209.1803288110.1159%2F000111569
Basyigit I, Yildiz F, Ozkara SK, Yildirim E, Boyaci H, Ilgazli A: The effect of clarithromycin on inflammatory markers in chronic obstructive pulmonary disease: preliminary data. Ann Pharmacother 2004;38:1400–1405.1525219110.1345%2Faph.1D634
Rosell A, Monsó E, Soler N, Torres F, Angrill J, Riise G, et al: Microbiologic determinants of exacerbation in chronic obstructive pulmonary disease. Arch Intern Med 2005;165:891–897.1585164010.1001%2Farchinte.165.8.891
Stănescu D, Sanna A, Veriter C, Kostianev S, Calcagni PG, Fabbri LM, Maestrelli P: Airways obstruction, chronic expectoration, and rapid decline of FEV1 in smokers are associated with increased levels of sputum neutrophils. Thorax 1996;51:267–271.877912910.1136%2Fthx.51.3.267
Barnes PJ: Emerging pharmacotherapies for COPD. Chest 2008;134:1278–1286.1905995810.1378%2Fchest.08-1385
Crosbie PA, Woodhead MA: Long-term macrolide therapy in chronic inflammatory airway diseases. Eur Respir J 2009;33:171–181.1911822810.1183%2F09031936.00042208
King P: Is there a role for inhaled corticosteroids and macrolide therapy in bronchiectasis? Drugs 2007;67:965–974.1748814210.2165%2F00003495-200767070-00002
Keicho N, Kudoh S: Diffuse panbronchiolitis: role of macrolides in therapy. Am J Respir Med 2002;1:119–131.14720066
Patel IS, Seemungal TA, Wilks M, Lloyd-Owen SJ, Donaldson GC, Wedzicha JA: Relationship between bacterial colonisation and the frequency, character, and severity of COPD exacerbations. Thorax 2002;57:759–764.1220051810.1136%2Fthorax.57.9.759
Rubin BK, Henke MO: Immunomodulatory activity and effectiveness of macrolides in chronic airway disease. Chest 2004;125:70S–78S.1487200310.1378%2Fchest.125.2_suppl.70S
Gotfried MH: Macrolides for the treatment of chronic sinusitis, asthma, and COPD. Chest 2004;125:52S–60S.1487200110.1378%2Fchest.125.2_suppl.52S
Hahn DL: Macrolide therapy in asthma: limited treatment, long-term improvement. Eur Respir J 2009;33:1239.1940706210.1183%2F09031936.00000209
Aaron SD, Angel JB, Lunau M, Wright K, Fex C, Le Saux N, et al: Granulocyte inflammatory markers and airway infection during acute exacerbation of chronic obstructive pulmonary disease. Am J Respir Crit Care Med 2001;163:349–355.11179105
Cazzola M, MacNee W, Martinez FJ, Rabe KF, Franciosi LG, Barnes PJ, et al: Outcomes for COPD pharmacological trials: from lung function to biomarkers. Eur Respir J 2008;31:416–469.1823895110.1183%2F09031936.00099306
Jones PW, Quirk FH, Baveystock CM, Littlejohns P: A self-complete measure of health status for chronic airflow limitation. The St. George’s Respiratory Questionnaire. Am Rev Respir Dis 1992;145:1321–1327.1595997
Suzuki T, Yanai M, Yamaya M, Satoh-Nakagawa T, Sekizawa K, Ishida S, et al: Erythromycin and common cold in COPD. Chest 2001;120:730–733.1155550110.1378%2Fchest.120.3.730
Banerjee D, Khair OA, Honeybourne D: The effect of oral clarithromycin on health status and sputum bacteriology in stable COPD. Respir Med 2005;99:208–215.1571518810.1016%2Fj.rmed.2004.06.009
Seemungal TA, Wilkinson TM, Hurst JR, Perera WR, Sapsford RJ, Wedzicha JA: Long-term erythromycin therapy is associated with decreased chronic obstructive pulmonary disease exacerbations. Am J Respir Crit Care Med 2008;178:1139–1147.1872343710.1164%2Frccm.200801-145OC
Desaki M, Takizawa H, Ohtoshi T, Kasama T, Kobayashi K, Sunazuka T, et al: Erythromycin suppresses nuclear factor-ĸB and activator protein-1 activation in human bronchial epithelial cells. Biochem Biophys Res Commun 2000;267:124–128.1062358510.1006%2Fbbrc.1999.1917
Nagai H, Shishido H, Yoneda R, Yamaguchi E, Tamura A, Kurashima A: Long-term low-dose administration of erythromycin to patients with diffuse panbronchiolitis. Respiration 1991;58:145–149.174584510.1159%2F000195915
Burge PS, Calverley PM, Jones PW, Spencer S, Anderson JA, Maslen TK: Randomised, double blind, placebo controlled study of fluticasone propionate in patients with moderate to severe chronic obstructive pulmonary disease: the ISOLDE trial. BMJ 2000;320:1297–1303.1080761910.1136%2Fbmj.320.7245.1297
Hodge S, Hodge G, Brozyna S, Jersmann H, Holmes M, Reynolds PN: Azithromycin increases phagocytosis of apoptotic bronchial epithelial cells by alveolar macrophages. Eur Respir J 2006;28:486–495.1673799210.1183%2F09031936.06.00001506
Simpson JL, Powell H, Boyle MJ, Scott RJ, Gibson PG: Clarithromycin targets neutrophilic airway inflammation in refractory asthma. Am J Respir Crit Care Med 2008;177:148–155.1794761110.1164%2Frccm.200707-1134OC
van Eeden SF, Sin DD: Chronic obstructive pulmonary disease: a chronic systemic inflammatory disease. Respiration 2008;75:224–238.1804297810.1159%2F000111820
Pauwels RA, Rabe KF: Burden and clinical features of chronic obstructive pulmonary disease (COPD). Lancet 2004;364:613–620.1531336310.1016%2FS0140-6736%2804%2916855-4
Calverley PM, Walker P: Chronic obstructive pulmonary disease. Lancet 2003;362:1053–1061.1452253710.1016%2FS0140-6736%2803%2914416-9
Yamaryo T, Oishi K, Yoshimine H, Tsuchihashi Y, Matsushima K, Nagatake T: Fourteen-member macrolides promote the phosphatidylserine receptor-dependent phagocytosis of apoptotic neutrophils by alveolar macrophages. Antimicrob Agents Chemother 2003;47:48–53.1249916810.1128%2FAAC.47.1.48-53.2003
Tamaoki J: The effects of macrolides on inflammatory cells. Chest 2004;125:41S–50S.1487200010.1378%2Fchest.125.2_suppl.41S
Ronchi MC, Piragino C, Rosi E, Amendola M, Duranti R, Scano G: Role of sputum differential cell count in detecting airway inflammation in patients with chronic bronchial asthma or COPD. Thorax 1996;51:1000–1004.897760010.1136%2Fthx.51.10.1000
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21079411 - Respiration. 2010;80(6):441-2
References_xml – reference: Saraiva-Romanholo BM, Barnabé V, Carvalho AL, Martins MA, Saldiva PH, Nunes Mdo P: Comparison of three methods for differential cell count in induced sputum. Chest 2003;124:1060–1066.1297003810.1378%2Fchest.124.3.1060
– reference: Gotfried MH: Macrolides for the treatment of chronic sinusitis, asthma, and COPD. Chest 2004;125:52S–60S.1487200110.1378%2Fchest.125.2_suppl.52S
– reference: van Eeden SF, Sin DD: Chronic obstructive pulmonary disease: a chronic systemic inflammatory disease. Respiration 2008;75:224–238.1804297810.1159%2F000111820
– reference: Keicho N, Kudoh S: Diffuse panbronchiolitis: role of macrolides in therapy. Am J Respir Med 2002;1:119–131.14720066
– reference: Hahn DL: Macrolide therapy in asthma: limited treatment, long-term improvement. Eur Respir J 2009;33:1239.1940706210.1183%2F09031936.00000209
– reference: Seemungal TA, Wilkinson TM, Hurst JR, Perera WR, Sapsford RJ, Wedzicha JA: Long-term erythromycin therapy is associated with decreased chronic obstructive pulmonary disease exacerbations. Am J Respir Crit Care Med 2008;178:1139–1147.1872343710.1164%2Frccm.200801-145OC
– reference: Desaki M, Takizawa H, Ohtoshi T, Kasama T, Kobayashi K, Sunazuka T, et al: Erythromycin suppresses nuclear factor-ĸB and activator protein-1 activation in human bronchial epithelial cells. Biochem Biophys Res Commun 2000;267:124–128.1062358510.1006%2Fbbrc.1999.1917
– reference: Banerjee D, Khair OA, Honeybourne D: The effect of oral clarithromycin on health status and sputum bacteriology in stable COPD. Respir Med 2005;99:208–215.1571518810.1016%2Fj.rmed.2004.06.009
– reference: Rabe KF, Hurd S, Anzueto A, Barnes PJ, Buist SA, Calverley P, et al: Global strategy for the diagnosis, management, and prevention of chronic obstructive pulmonary disease: GOLD executive summary. Am J Respir Crit Care Med 2007;176:532–555.1750754510.1164%2Frccm.200703-456SO
– reference: Giamarellos-Bourboulis EJ: Macrolides beyond the conventional antimicrobials: a class of potent immunomodulators. Int J Antimicrob Agents 2008;31:12–20.1793594910.1016%2Fj.ijantimicag.2007.08.001
– reference: Stănescu D, Sanna A, Veriter C, Kostianev S, Calcagni PG, Fabbri LM, Maestrelli P: Airways obstruction, chronic expectoration, and rapid decline of FEV1 in smokers are associated with increased levels of sputum neutrophils. Thorax 1996;51:267–271.877912910.1136%2Fthx.51.3.267
– reference: He Z, Li B, Yu L, Liu Q, Zhong N, Ran P: Suppression of oxidant-induced glutathione synthesis by erythromycin in human bronchial epithelial cells. Respiration 2008;75:202–209.1803288110.1159%2F000111569
– reference: Barnes PJ: Emerging pharmacotherapies for COPD. Chest 2008;134:1278–1286.1905995810.1378%2Fchest.08-1385
– reference: Sethi S, Murphy TF: Infection in the pathogenesis and course of chronic obstructive pulmonary disease. N Engl J Med 2008;359:2355–2365.1903888110.1056%2FNEJMra0800353
– reference: Rosell A, Monsó E, Soler N, Torres F, Angrill J, Riise G, et al: Microbiologic determinants of exacerbation in chronic obstructive pulmonary disease. Arch Intern Med 2005;165:891–897.1585164010.1001%2Farchinte.165.8.891
– reference: Patel IS, Seemungal TA, Wilks M, Lloyd-Owen SJ, Donaldson GC, Wedzicha JA: Relationship between bacterial colonisation and the frequency, character, and severity of COPD exacerbations. Thorax 2002;57:759–764.1220051810.1136%2Fthorax.57.9.759
– reference: Tamaoki J: The effects of macrolides on inflammatory cells. Chest 2004;125:41S–50S.1487200010.1378%2Fchest.125.2_suppl.41S
– reference: Calverley PM, Walker P: Chronic obstructive pulmonary disease. Lancet 2003;362:1053–1061.1452253710.1016%2FS0140-6736%2803%2914416-9
– reference: Pauwels RA, Rabe KF: Burden and clinical features of chronic obstructive pulmonary disease (COPD). Lancet 2004;364:613–620.1531336310.1016%2FS0140-6736%2804%2916855-4
– reference: Banerjee D, Honeybourne D, Khair OA: The effect of oral clarithromycin on bronchial airway inflammation in moderate-to-severe stable COPD: a randomized controlled trial. Treat Respir Med 2004;3:59–65.1517489410.2165%2F00151829-200403010-00007
– reference: Nagai H, Shishido H, Yoneda R, Yamaguchi E, Tamura A, Kurashima A: Long-term low-dose administration of erythromycin to patients with diffuse panbronchiolitis. Respiration 1991;58:145–149.174584510.1159%2F000195915
– reference: King P: Is there a role for inhaled corticosteroids and macrolide therapy in bronchiectasis? Drugs 2007;67:965–974.1748814210.2165%2F00003495-200767070-00002
– reference: Azuma A, Kudoh S: Diffuse panbronchiolitis in East Asia. Respirology 2006;11:249–261.1663508210.1111%2Fj.1440-1843.2006.00845.x
– reference: Aaron SD, Angel JB, Lunau M, Wright K, Fex C, Le Saux N, et al: Granulocyte inflammatory markers and airway infection during acute exacerbation of chronic obstructive pulmonary disease. Am J Respir Crit Care Med 2001;163:349–355.11179105
– reference: Simpson JL, Powell H, Boyle MJ, Scott RJ, Gibson PG: Clarithromycin targets neutrophilic airway inflammation in refractory asthma. Am J Respir Crit Care Med 2008;177:148–155.1794761110.1164%2Frccm.200707-1134OC
– reference: Suzuki T, Yanai M, Yamaya M, Satoh-Nakagawa T, Sekizawa K, Ishida S, et al: Erythromycin and common cold in COPD. Chest 2001;120:730–733.1155550110.1378%2Fchest.120.3.730
– reference: Crosbie PA, Woodhead MA: Long-term macrolide therapy in chronic inflammatory airway diseases. Eur Respir J 2009;33:171–181.1911822810.1183%2F09031936.00042208
– reference: Basyigit I, Yildiz F, Ozkara SK, Yildirim E, Boyaci H, Ilgazli A: The effect of clarithromycin on inflammatory markers in chronic obstructive pulmonary disease: preliminary data. Ann Pharmacother 2004;38:1400–1405.1525219110.1345%2Faph.1D634
– reference: Burge PS, Calverley PM, Jones PW, Spencer S, Anderson JA, Maslen TK: Randomised, double blind, placebo controlled study of fluticasone propionate in patients with moderate to severe chronic obstructive pulmonary disease: the ISOLDE trial. BMJ 2000;320:1297–1303.1080761910.1136%2Fbmj.320.7245.1297
– reference: Cazzola M, MacNee W, Martinez FJ, Rabe KF, Franciosi LG, Barnes PJ, et al: Outcomes for COPD pharmacological trials: from lung function to biomarkers. Eur Respir J 2008;31:416–469.1823895110.1183%2F09031936.00099306
– reference: Rubin BK, Henke MO: Immunomodulatory activity and effectiveness of macrolides in chronic airway disease. Chest 2004;125:70S–78S.1487200310.1378%2Fchest.125.2_suppl.70S
– reference: Jones PW, Quirk FH, Baveystock CM, Littlejohns P: A self-complete measure of health status for chronic airflow limitation. The St. George’s Respiratory Questionnaire. Am Rev Respir Dis 1992;145:1321–1327.1595997
– reference: Sant’Anna CA, Stelmach R, Zanetti Feltrin MI, Filho WJ, Chiba T, Cukier A: Evaluation of health-related quality of life in low-income patients with COPD receiving long-term oxygen therapy. Chest 2003;123:136–141.1252761410.1378%2Fchest.123.1.136
– reference: Hodge S, Hodge G, Brozyna S, Jersmann H, Holmes M, Reynolds PN: Azithromycin increases phagocytosis of apoptotic bronchial epithelial cells by alveolar macrophages. Eur Respir J 2006;28:486–495.1673799210.1183%2F09031936.06.00001506
– reference: Ronchi MC, Piragino C, Rosi E, Amendola M, Duranti R, Scano G: Role of sputum differential cell count in detecting airway inflammation in patients with chronic bronchial asthma or COPD. Thorax 1996;51:1000–1004.897760010.1136%2Fthx.51.10.1000
– reference: Oishi K, Sonoda F, Kobayashi S, Iwagaki A, Nagatake T, Matsushima K, et al: Role of interleukin-8 (IL-8) and an inhibitory effect of erythromycin on IL-8 release in the airways of patients with chronic airway diseases. Infect Immun 1994;62:4145–4152.7927669
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Snippet Background: Chronic obstructive pulmonary disease (COPD) is characterized by airway inflammation and is associated with acute exacerbations. Macrolide...
Chronic obstructive pulmonary disease (COPD) is characterized by airway inflammation and is associated with acute exacerbations. Macrolide antibiotics have...
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SubjectTerms Aged
Allergies
Anti-Bacterial Agents - administration & dosage
Anti-Bacterial Agents - adverse effects
Antibacterial agents
Antibiotics. Antiinfectious agents. Antiparasitic agents
Biological and medical sciences
Bones, joints and connective tissue. Antiinflammatory agents
Cells
Chronic obstructive pulmonary disease
Chronic obstructive pulmonary disease, asthma
Clinical Investigations
Double-Blind Method
Drug therapy
Erythromycin - administration & dosage
Erythromycin - adverse effects
Female
Humans
Inflammatory diseases
Leukocyte Count
Leukocyte Elastase - analysis
Male
Medical sciences
Middle Aged
Pharmacology. Drug treatments
Pneumology
Pulmonary Disease, Chronic Obstructive - drug therapy
Pulmonary Disease, Chronic Obstructive - immunology
Quality of Life
Sputum - cytology
Sputum - drug effects
Sputum - immunology
Sputum - microbiology
Treatment Outcome
Title Effect of 6 Months of Erythromycin Treatment on Inflammatory Cells in Induced Sputum and Exacerbations in Chronic Obstructive Pulmonary Disease
URI https://karger.com/doi/10.1159/000321374
https://www.ncbi.nlm.nih.gov/pubmed/20881376
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Volume 80
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