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- Publisher Website: 10.1053/rmed.2001.1155
- Scopus: eid_2-s2.0-0034764130
- PMID: 11601743
- WOS: WOS:000171557600004
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Article: Macrophages, neutrophils and tumour necrosis factor-α expression in bronchiectatic airways in vivo
Title | Macrophages, neutrophils and tumour necrosis factor-α expression in bronchiectatic airways in vivo |
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Authors | |
Keywords | Airway biopsy Bronchiectasis Macrophages Neutrophils |
Issue Date | 2001 |
Publisher | Elsevier Ltd. The Journal's web site is located at http://www.elsevier.com/locate/rmed |
Citation | Respiratory Medicine, 2001, v. 95 n. 10, p. 792-798 How to Cite? |
Abstract | Bronchiectasis is increasingly being recognized as an inflammatory condition of the airways in which pathological permanent dilation occurs. We have obtained endobronchial biopsies in 14 patients with stable bronchiectasis and 15 control subjects. Airway neutrophils, macrophages and tumour necrosis factor-α (TNFα)-positive cells were stained with monoclonal antibodies and the densities of positive cells in the lamina propria were determined by using a computer image analyser. There was significantly higher neutrophil, macrophage and TNFα-positive cell densities in the lamina propria of bronchiectatic than control airways (P<0·001, P<0·001 and P=0·0002, respectively). Airway neutrophil density, in bronchiectasis but not in controls, correlated with TNFα-positive cell density (r=0·71, P=0·004). A significant correlation between airway macrophage and TNFα-positive cell densities was demonstrated in both control and bronchiectatic airways (r=0·63, P=0·016 and r=0·60, P=0·02 respectively). Neutrophil density negatively correlated with per cent forced vital capacity (FVC%) predicted among patients with bronchiectasis (r=-0·53, P=0·04). Bronchiectasis patients who were regular sputum producers had a significantly higher macrophage, but not neutrophil density, than their counterparts (P=0·02 and P=0·48 respectively). Our original findings suggest that airway macrophages could contribute to neutrophil influx into airway walls through their production of TNFα and therefore play an important role in the pathogenesis of bronchiectasis. © 2001 Harcourt Publishers Ltd. |
Persistent Identifier | http://hdl.handle.net/10722/149598 |
ISSN | 2023 Impact Factor: 3.5 2023 SCImago Journal Rankings: 1.180 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Zheng, L | en_US |
dc.contributor.author | Shum, IH | en_US |
dc.contributor.author | Tipoe, GL | en_US |
dc.contributor.author | Leung, R | en_US |
dc.contributor.author | Lam, WK | en_US |
dc.contributor.author | Ooi, GC | en_US |
dc.contributor.author | Tsang, KW | en_US |
dc.date.accessioned | 2012-06-26T05:55:45Z | - |
dc.date.available | 2012-06-26T05:55:45Z | - |
dc.date.issued | 2001 | en_US |
dc.identifier.citation | Respiratory Medicine, 2001, v. 95 n. 10, p. 792-798 | en_US |
dc.identifier.issn | 0954-6111 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/149598 | - |
dc.description.abstract | Bronchiectasis is increasingly being recognized as an inflammatory condition of the airways in which pathological permanent dilation occurs. We have obtained endobronchial biopsies in 14 patients with stable bronchiectasis and 15 control subjects. Airway neutrophils, macrophages and tumour necrosis factor-α (TNFα)-positive cells were stained with monoclonal antibodies and the densities of positive cells in the lamina propria were determined by using a computer image analyser. There was significantly higher neutrophil, macrophage and TNFα-positive cell densities in the lamina propria of bronchiectatic than control airways (P<0·001, P<0·001 and P=0·0002, respectively). Airway neutrophil density, in bronchiectasis but not in controls, correlated with TNFα-positive cell density (r=0·71, P=0·004). A significant correlation between airway macrophage and TNFα-positive cell densities was demonstrated in both control and bronchiectatic airways (r=0·63, P=0·016 and r=0·60, P=0·02 respectively). Neutrophil density negatively correlated with per cent forced vital capacity (FVC%) predicted among patients with bronchiectasis (r=-0·53, P=0·04). Bronchiectasis patients who were regular sputum producers had a significantly higher macrophage, but not neutrophil density, than their counterparts (P=0·02 and P=0·48 respectively). Our original findings suggest that airway macrophages could contribute to neutrophil influx into airway walls through their production of TNFα and therefore play an important role in the pathogenesis of bronchiectasis. © 2001 Harcourt Publishers Ltd. | en_US |
dc.language | eng | en_US |
dc.publisher | Elsevier Ltd. The Journal's web site is located at http://www.elsevier.com/locate/rmed | en_US |
dc.relation.ispartof | Respiratory Medicine | en_US |
dc.subject | Airway biopsy | - |
dc.subject | Bronchiectasis | - |
dc.subject | Macrophages | - |
dc.subject | Neutrophils | - |
dc.subject.mesh | Aged | en_US |
dc.subject.mesh | Antigens, Cd - Analysis | en_US |
dc.subject.mesh | Antigens, Differentiation, Myelomonocytic - Analysis | en_US |
dc.subject.mesh | Biological Markers - Analysis | en_US |
dc.subject.mesh | Bronchiectasis - Immunology - Pathology | en_US |
dc.subject.mesh | Bronchoscopy | en_US |
dc.subject.mesh | Case-Control Studies | en_US |
dc.subject.mesh | Cell Count | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Immunohistochemistry | en_US |
dc.subject.mesh | Lung - Immunology - Pathology | en_US |
dc.subject.mesh | Macrophages - Metabolism - Pathology | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Middle Aged | en_US |
dc.subject.mesh | Neutrophils - Metabolism - Pathology | en_US |
dc.subject.mesh | Pancreatic Elastase - Analysis | en_US |
dc.subject.mesh | Statistics, Nonparametric | en_US |
dc.subject.mesh | Tumor Necrosis Factor-Alpha - Metabolism | en_US |
dc.title | Macrophages, neutrophils and tumour necrosis factor-α expression in bronchiectatic airways in vivo | en_US |
dc.type | Article | en_US |
dc.identifier.email | Tipoe, GL:tgeorge@hkucc.hku.hk | en_US |
dc.identifier.authority | Tipoe, GL=rp00371 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1053/rmed.2001.1155 | en_US |
dc.identifier.pmid | 11601743 | - |
dc.identifier.scopus | eid_2-s2.0-0034764130 | en_US |
dc.identifier.hkuros | 68134 | - |
dc.identifier.hkuros | 64250 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-0034764130&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 95 | en_US |
dc.identifier.issue | 10 | en_US |
dc.identifier.spage | 792 | en_US |
dc.identifier.epage | 798 | en_US |
dc.identifier.isi | WOS:000171557600004 | - |
dc.publisher.place | United Kingdom | en_US |
dc.identifier.scopusauthorid | Zheng, L=7403404086 | en_US |
dc.identifier.scopusauthorid | Shum, IH=6602960338 | en_US |
dc.identifier.scopusauthorid | Tipoe, GL=7003550610 | en_US |
dc.identifier.scopusauthorid | Leung, R=7101876102 | en_US |
dc.identifier.scopusauthorid | Lam, WK=7203021937 | en_US |
dc.identifier.scopusauthorid | Ooi, GC=7006176119 | en_US |
dc.identifier.scopusauthorid | Tsang, KW=7201555024 | en_US |
dc.identifier.issnl | 0954-6111 | - |