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dc.contributor.authorGarratt, L.
dc.contributor.authorWright, A.
dc.contributor.authorRanganathan, S.
dc.contributor.authorGrigg, J.
dc.contributor.authorSly, P.
dc.contributor.authorDouglas, T.
dc.contributor.authorGangell, C.
dc.contributor.authorHall, Graham
dc.contributor.authorKicic, A.
dc.contributor.authorMott, L.
dc.contributor.authorSkoric, B.
dc.date.accessioned2017-07-27T05:21:05Z
dc.date.available2017-07-27T05:21:05Z
dc.date.created2017-07-26T11:11:12Z
dc.date.issued2012
dc.identifier.citationGarratt, L. and Wright, A. and Ranganathan, S. and Grigg, J. and Sly, P. and Douglas, T. and Gangell, C. et al. 2012. Small macrophages are present in early childhood respiratory disease. Journal of Cystic Fibrosis. 11 (3): pp. 201-208.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/54466
dc.identifier.doi10.1016/j.jcf.2011.11.008
dc.description.abstract

Background: Recently, an established "small macrophage" phenotype has been observed in the sputum of patients with CF and COPD. However, little is known about the prevalence of this phenotype in the airways of young children. Since respiratory inflammation begins early in CF, we hypothesised that these small macrophages would be increased in paediatric CF bronchoalveolar lavage (BAL). Methods: Macrophage populations in CF and disease control BAL were assessed by multicolour flow cytometry. BAL inflammatory indices were collected as part of the AREST-CF programme. Results: Small macrophages were present in CF (n = 35, mean 36 ± 12% of BAL macrophages) but not significantly different to the respiratory disease controls (n = 7, mean 40 ± 21%). Number of small macrophages correlated significantly with number of BAL neutrophils (r = 0.44, p< 0.01) but not infection or IL-8. Conclusions: In paediatric patients small macrophages are not unique to CF, but their establishment as the dominant phenotype in adults may be due to chronicity of inflammation and infection.

dc.publisherElsevier
dc.titleSmall macrophages are present in early childhood respiratory disease
dc.typeJournal Article
dcterms.source.volume11
dcterms.source.number3
dcterms.source.startPage201
dcterms.source.endPage208
dcterms.source.issn1569-1993
dcterms.source.titleJournal of Cystic Fibrosis
curtin.departmentSchool of Physiotherapy and Exercise Science
curtin.accessStatusOpen access via publisher


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