Volume 121, Issue 6 , Pages 1460-1466.e7, June 2008
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-γ (P < .001) production. Consistent with other reports, effector CD4+ T-cell responses (IFN-γ and IL-13) tended to be lower in the allergic group. These neonates showed less significant Treg cell–associated suppression of IFN-γ (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-γ effector responses compared with that seen in the nonallergic group (78%, P = .015). The magnitude of suppression (change in IFN-γ 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.
Key words: Regulatory T cells, cord blood, neonates, food allergy, allergic disease, egg allergy, cytokines, infants
Abbreviations used: CBMC, Cord blood mononuclear cell, HDM, House dust mite, OVA, Ovalbumin, SEB, Staphylococcal endotoxin B, SPT, Skin prick test, Treg, Regulatory T
S.L.P. is funded by the National Health and Medical Research Council (NHMRC) of Australia. The project used the flow cytometry facility, which was funded by a Centre of Excellence grant from the Western Australian government and is located at the Telethon Institute for Child Health Research.
Disclosure of potential conflict of interest: The authors have declared that they have received research support from the National Health and Medical Research Council of Australia.
PII: S0091-6749(08)00609-X
doi:10.1016/j.jaci.2008.03.025
© 2008 American Academy of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.
Volume 121, Issue 6 , Pages 1460-1466.e7, June 2008
