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LETTER |
Luton & Dunstable Hospital, Luton, Bedfordshire LU4 0DZ, UK; michael_eisenhut@yahoo.com
Keywords: respiratory syncytial virus; bronchiolitis; bacterial co-infection; children; paediatric intensive care
| The first 150 words of the full text of this article appear below. |
Thorburn et al reported on pulmonary bacterial co-infection in children with severe respiratory syncytial virus (RSV) bronchiolitis.1 The authors found that 40% of children with severe RSV infection were infected with bacteria in their lower airways. The most commonly isolated organism was Haemophilus influenzae, a Gram negative lipopolysaccharide producing organism.
Previous studies from the same paediatric intensive care unit have investigated cytokines, chemokines, and the cellular composition of specimens obtained by non-bronchoscopic bronchoalveolar lavage (BAL) in ventilated children with RSV infection using the same method as was used in this study.2,3 The investigators found a predominance of neutrophil leucocytes, increased production of interleukin (IL)-9,2 and increased levels of a number of chemokines3 compared with controls without lower respiratory tract infection.
Lipopolysaccharide, as produced by H influenzae, is a potent activator of the nuclear transcription factor NF-
B.4 NF-
B is essential in activating IL-9 production5 and in the
Related Article
Thorax 2007 62: 278.
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