Arch. Dis. Child

HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS REGISTER
[Advanced]

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this link to a friend
Right arrow Similar articles in ADC Online
Right arrow Similar articles in PubMed
Right arrow Add article to my folders
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Currie, A E
Right arrow Articles by Kotecha, S
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Currie, A E
Right arrow Articles by Kotecha, S
Archives of Disease in Childhood Fetal and Neonatal Edition 2002;86:F193-F197
© 2002 Archives of Disease in Childhood Fetal and Neonatal Edition


ORIGINAL ARTICLE

Fibroblast mitogenic activity of lung lavage fluid from infants with chronic lung disease of prematurity

A E Currie, M Kelly, J R Vyas, H Pandya, D Field, S Kotecha

Department of Child Health, University of Leicester, Leicester LE2 7LX, UK

Correspondence to:
Correspondence to:
Dr Kotecha, Department of Child Health, University of Leicester, Leicester LE2 7LX, UK;
sk43{at}le.ac.uk

Background: Lung fibrosis is thought to be important in chronic lung disease of prematurity (CLD).

Methods: Fibroblast proliferative activity was assessed in 207 bronchoalveolar lavage fluid (BALF) samples from 43 infants. Sixteen developed CLD (birth weight 765 g (630–1230), gestation 26.5 weeks (23–29)), 18 developed respiratory distress syndrome (RDS) (birth weight 1415 g (430–4160), gestation 31 weeks (23–39)), and nine control infants (birth weight 2110 g (900–3720), gestation 32 weeks (26–41)) received mechanical ventilation for non-pulmonary reasons.

Results: The fibroblast proliferative activity relative to 10% fetal calf serum was 64–75% in infants with CLD, 55–86% in the RDS group, and 42–68% in control infants during the first 5 weeks of life. Only at day 3 was there a difference between the groups (CLD 72% v control 42%, p < 0.01; RDS 63% v control 42%, p < 0.05). With the use of neutralising antibodies, platelet derived growth factor BB (PDGF-BB) and epidermal growth factor were undetectable, and insulin-like growth factor I (IGF-I) accounted for 14% (p < 0.05) and 11% (p < 0.005) of BALF mitogenic activity from the RDS and CLD groups respectively.

Conclusions: The mitogenic activity of BALF was similar in the three groups studied and was only partially accounted for by IGF-I. Growth factors other than PDGF-BB and IGF-I contribute significantly to this process.


Keywords: chronic lung disease of prematurity; bronchopulmonary dysplasia; growth factors; fibroblasts

Abbreviations: CLD, chronic lung disease of prematurity; RDS, respiratory distress syndrome; TGF, transforming growth factor; BAL, bronchoalveolar lavage; BALF, bronchoalveolar lavage fluid; PDGF-BB, platelet derived growth factor B; IGF-I, insulin-like growth factor I; FCS, fetal calf serum; FGM, fibroblast growth medium; EGF, epidermal growth factor




This article has been cited by other articles:


Home page
Eur Respir JHome page
W.A. Dik, M.A. Versnel, B.A. Naber, D.J. Janssen, A.H. van Kaam, and L.J.I. Zimmermann
Dexamethasone treatment does not inhibit fibroproliferation in chronic lung disease of prematurity
Eur. Respir. J., May 1, 2003; 21(5): 842 - 847.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS REGISTER
ARCH DIS CHILD FETAL NEONATAL ED ED PRACTICE
Terms and conditions relating to subscriptions purchased online  ¦  Website terms and conditions  ¦  Privacy policy
Copyright © 2002 BMJ Publishing Group Ltd & Royal College of Paediatrics and Child Health