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The effects of increased oily fish intake during pregnancy on neonatal immune cells – results from the salmon in pregnancy study (SIPS)

Published online by Cambridge University Press:  04 June 2010

P. S. Noakes
Affiliation:
Institute of Human Nutrition and DOHaD Division, School of Medicine, University of Southampton, IDS Building, Southampton General Hospital, SouthamptonSO16 6YD, UK
M. Vlachava
Affiliation:
Institute of Human Nutrition and DOHaD Division, School of Medicine, University of Southampton, IDS Building, Southampton General Hospital, SouthamptonSO16 6YD, UK
L.-S. Kremmyda
Affiliation:
Institute of Human Nutrition and DOHaD Division, School of Medicine, University of Southampton, IDS Building, Southampton General Hospital, SouthamptonSO16 6YD, UK
N. D. Diaper
Affiliation:
Institute of Human Nutrition and DOHaD Division, School of Medicine, University of Southampton, IDS Building, Southampton General Hospital, SouthamptonSO16 6YD, UK
E. A. Miles
Affiliation:
Institute of Human Nutrition and DOHaD Division, School of Medicine, University of Southampton, IDS Building, Southampton General Hospital, SouthamptonSO16 6YD, UK
P. C. Calder
Affiliation:
Institute of Human Nutrition and DOHaD Division, School of Medicine, University of Southampton, IDS Building, Southampton General Hospital, SouthamptonSO16 6YD, UK
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Abstract

Type
Abstract
Copyright
Copyright © The Authors 2009

The development of childhood allergic disease is frequently preceded by immunologic differences that are most evident in the neonatal period(Reference Prescott, Macaubas and Smallacombe1). Preliminary studies also suggest that maternal environmental exposures (such as diet) can modify neonatal T-cell function, although the mechanisms are not clear(Reference Willers, Devereux and Craig2). With rising allergic disease rates, there is a continuing urgency to identify the pathways involved and to explore the effects of early interventions that could favourably influence the functional development of T-cell responses and prevent allergic disease. Dietary n–3 polyunsaturated fatty acids (PUFA), found in oily fish and in fish oils, may represent a mode of allergy prevention. Fish oil supplementation during pregnancy alters neonatal immunity in a way that would be consistent with lowered risk of atopy(Reference Dunstan, Mori and Bardent3). However, there are no studies of the influence of increased oily fish consumption in pregnancy on neonatal immune cell phenotypes.

At 20 weeks gestation, 123 allergic, pregnant women with low habitual intake of oily fish (⩽2/month) were randomised to consume two portions of salmon per week (each portion of salmon provided about 2 g of n–3 PUFA) or to continue their habitual diet of low oily fish consumption until delivery. Mononuclear cells were purified from umbilical cord blood (n=101) and the percentages of T-regulatory cells (defined as CD4+CD25+CD127lo/− cells) and monocytes (defined as CD14+TLR-2+ cells) were examined by flow cytometry following staining the cells with relevant fluorescently labelled antibodies. Percentages of cord blood T-regulatory cells and monocytes were not different between the control and oily fish intervention groups (P=0.727 and P=0.364, respectively). Similarly, surface expression of CD25+CD127lo/−on CD4+ T-cells (mean fluorescence intensity) was not different between the two groups (P=0.159).

In conclusion, oily fish intervention in pregnancy does not alter numbers of neonatal regulatory T-cells or TLR-2 expressing monocytes. Further assessment of cellular immune function and clinical follow-up of these infants will determine if there are any significant effects of maternal oily fish intake on postnatal immune development and expression of allergic disease.

This work was supported by the European Commission under Framework 6 and forms part of the AquaMax integrated project (FOOD-CT-2006-016249-2). The authors wish to thank staff at the Princess Anne Hospital, Southampton and the Medical Research Council Epidemiology Resource Centre for their invaluable contributions to this study.

References

1.Prescott, S, Macaubas, C, Smallacombe, T et al. (1999) Lancet 353, 196200.CrossRefGoogle Scholar
2.Willers, S, Devereux, G, Craig, L et al. (2007) Thorax 62, 773779.CrossRefGoogle Scholar
3.Dunstan, JA, Mori, TA, Bardent, A et al. (2003) Clin Exp Allergy 33, 442448.CrossRefGoogle Scholar