The University of Southampton
University of Southampton Institutional Repository

Children with egg allergy have evidence of reduced neonatal CD4+CD25+CD127lo/- regulatory T cell function

Children with egg allergy have evidence of reduced neonatal CD4+CD25+CD127lo/- regulatory T cell function
Children with egg allergy have evidence of reduced neonatal CD4+CD25+CD127lo/- regulatory T cell function
Background: The role of regulatory T (Treg) cells in allergic predisposition is not known.

Objective: This study compared the frequency and function of cord blood Treg cells from nonallergic children (n = 18) with those from children who have egg allergy (n = 15) in the first year of life.

Methods: CD4+ effector T cells and autologous antigen-presenting cells isolated from cord blood mononuclear cells were cocultured with or without CD4+CD25+CD127lo/? Treg cells, and cytokine responses to staphylococcal endotoxin B were assessed after 48 hours.

Results: The addition of Treg cell populations to cord blood mononuclear cell cultures resulted in significant reduction in IL-10 (P = .002), IL-13 (P = .012), and IFN-? (P < .001) production. Consistent with other reports, effector CD4+ T-cell responses (IFN-? and IL-13) tended to be lower in the allergic group. These neonates showed less significant Treg cell–associated suppression of IFN-? (P = .015) compared with that seen in the nonallergic group (P = .001). The allergic group was also less likely (44%) to show Treg cell–associated suppression of IFN-? effector responses compared with that seen in the nonallergic group (78%, P = .015). The magnitude of suppression (change in IFN-? level when CD4+CD25+CD127lo/? Treg cells were added to responding effector T-cell cultures) was significantly lower in the allergic group (P = .004). There were no between-group differences in the circulating CD4+CD25+CD127lo/? Treg cells (as a percentage of cord blood T cells) or in the FOXP3 expression of these cells.

Conclusion: This study confirms the presence and activity of Treg cells in cord blood and provides preliminary evidence of differences in neonates who progress to allergic disease in the first year of life.

regulatory t cells, cord blood, neonates, food allergy, allergic disease, egg allergy, cytokines, infants
0091-6749
1460-1466
Smith, Miranda
7919a542-c173-431e-b983-01356556b836
Tourigny, Michelle
149b0563-3ab5-4759-b777-0e47d40774f9
Noakes, Paul
0ed50cd9-de73-4851-8039-ee72860d8ae5
Thornton, Catherine
e91ddff8-1488-4930-a4db-48ce571e2ef8
Tulic, Meri
f4237d1d-fe22-4f2b-aae9-44600a4cf1ce
Prescott, Susan
a81e2cd6-dafc-464b-9ed3-4a9a0e24bbb6
Smith, Miranda
7919a542-c173-431e-b983-01356556b836
Tourigny, Michelle
149b0563-3ab5-4759-b777-0e47d40774f9
Noakes, Paul
0ed50cd9-de73-4851-8039-ee72860d8ae5
Thornton, Catherine
e91ddff8-1488-4930-a4db-48ce571e2ef8
Tulic, Meri
f4237d1d-fe22-4f2b-aae9-44600a4cf1ce
Prescott, Susan
a81e2cd6-dafc-464b-9ed3-4a9a0e24bbb6

Smith, Miranda, Tourigny, Michelle, Noakes, Paul, Thornton, Catherine, Tulic, Meri and Prescott, Susan (2008) Children with egg allergy have evidence of reduced neonatal CD4+CD25+CD127lo/- regulatory T cell function. Journal of Allergy and Clinical Immunology, 121 (6), 1460-1466. (doi:10.1016/j.jaci.2008.03.025). (PMID:18455222)

Record type: Article

Abstract

Background: The role of regulatory T (Treg) cells in allergic predisposition is not known.

Objective: This study compared the frequency and function of cord blood Treg cells from nonallergic children (n = 18) with those from children who have egg allergy (n = 15) in the first year of life.

Methods: CD4+ effector T cells and autologous antigen-presenting cells isolated from cord blood mononuclear cells were cocultured with or without CD4+CD25+CD127lo/? Treg cells, and cytokine responses to staphylococcal endotoxin B were assessed after 48 hours.

Results: The addition of Treg cell populations to cord blood mononuclear cell cultures resulted in significant reduction in IL-10 (P = .002), IL-13 (P = .012), and IFN-? (P < .001) production. Consistent with other reports, effector CD4+ T-cell responses (IFN-? and IL-13) tended to be lower in the allergic group. These neonates showed less significant Treg cell–associated suppression of IFN-? (P = .015) compared with that seen in the nonallergic group (P = .001). The allergic group was also less likely (44%) to show Treg cell–associated suppression of IFN-? effector responses compared with that seen in the nonallergic group (78%, P = .015). The magnitude of suppression (change in IFN-? level when CD4+CD25+CD127lo/? Treg cells were added to responding effector T-cell cultures) was significantly lower in the allergic group (P = .004). There were no between-group differences in the circulating CD4+CD25+CD127lo/? Treg cells (as a percentage of cord blood T cells) or in the FOXP3 expression of these cells.

Conclusion: This study confirms the presence and activity of Treg cells in cord blood and provides preliminary evidence of differences in neonates who progress to allergic disease in the first year of life.

This record has no associated files available for download.

More information

Published date: June 2008
Keywords: regulatory t cells, cord blood, neonates, food allergy, allergic disease, egg allergy, cytokines, infants

Identifiers

Local EPrints ID: 180643
URI: http://eprints.soton.ac.uk/id/eprint/180643
ISSN: 0091-6749
PURE UUID: 934b36b9-9fa6-4b91-a446-f6a81fa0210c
ORCID for Paul Noakes: ORCID iD orcid.org/0000-0002-2678-1971

Catalogue record

Date deposited: 12 Apr 2011 08:43
Last modified: 15 Mar 2024 03:27

Export record

Altmetrics

Contributors

Author: Miranda Smith
Author: Michelle Tourigny
Author: Paul Noakes ORCID iD
Author: Catherine Thornton
Author: Meri Tulic
Author: Susan Prescott

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×