Register for email alerts and news feeds:
This journal | BMJ Group
rss
Archives of Disease in Childhood 2002;86:431-433; doi:10.1136/adc.86.6.431
Copyright © 2002 BMJ Publishing Group Ltd & Royal College of Paediatrics and Child Health.
Archives of Disease in Childhood 2002;86:431-433
© 2002 Archives of Disease in Childhood

ORIGINAL ARTICLE

A hypothesis: antenatal sensitisation to respiratory syncytial virus in viral bronchiolitis

J P Legg1, C A Jones1, J A Warner1, S L Johnston2, J O Warner1

1 Department of Child Health, University of Southampton, Southampton, UK
2 University Medicine, University of Southampton, Southampton, UK and the National Heart and Lung Institute at St Mary's, London, UK

Correspondence to:
Correspondence to:
Dr J Legg, Department of Child Health, G Floor – Mail Point 803, Southampton General Hospital, Tremona Road, Southampton SO16 6YD, UK;
julianlegg{at}yahoo.co.uk

Aim: To investigate the possibility of antenatal sensitisation to respiratory syncytial virus (RSV).

Methods: A total of 36 cord blood specimens were obtained from newborn infants; serum IgA was measured to exclude maternal blood contamination. Cord peripheral blood mononuclear cells were separated and cultured in the presence of either uninfected negative control cells or cells containing ultraviolet (UV) inactivated RSV. Proliferation was assessed by tritiated thymidine incorporation. Supernatant cytokine concentrations were measured using ELISA.

Results: Significantly higher proliferative response rates to UV inactivated RSV were shown in those infants exposed in utero to the RSV epidemic after 22 weeks gestation. UV inactivated RSV stimulation induced significantly higher interferon {gamma} production from specimens with a positive proliferative response (sensitised) than from those with a negative response (not sensitised).

Conclusions: Antenatal sensitisation to RSV occurs in one third of infants exposed to an RSV epidemic at the appropriate time of gestation. This sensitisation is associated with increased interferon {gamma} production, suggesting a type 1 memory response. We hypothesise that priming of fetal T cells to RSV results in a reduced severity of subsequent RSV disease in these individuals and that this will explain much of the clinical diversity of RSV disease.

Keywords: respiratory syncytial virus; bronchiolitis; infant; newborn; fetal blood; T lymphocyte

Abbreviations: IFN, interferon; IL, interleukin; MOI, multiplicity of infection; PBMC, peripheral blood mononuclear cells; PHA, phytohaemagglutinin; RSV, respiratory syncytial virus; UV, ultraviolet; VB, viral bronchiolitis


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?

This Article

Services
Citing Articles
Google Scholar
PubMed
Topic Collections
Bookmark with

Register for free content

The full back archive is now available for all BMJ Journals. Institutional subscribers may access the entire archive as part of their subscription. Personal subscribers will also have access to all content when logged in. Non-subscribers who register have free access to all articles published before 2006 right back to volume 1 issue 1. Register here to access the free archive of all BMJ Journals.

Don't forget to sign up for content alerts so you keep up to date with all the articles as they are published.

Latest from ADC

 

ADC is co-owned by the RCPCH and is the official journal of the European Academy of Paediatrics

BMJ Careers - Latest Paediatrics and Paediatric Surgery Jobs

Paediatrics and Paediatric Surgery Jobs