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Research Article

Maternal and early postnatal polychlorinated biphenyl exposure in relation to total serum immunoglobulin concentrations in 6-month-old infants

, , , , , , , , , , , & show all
Pages 95-100 | Received 17 Sep 2010, Accepted 15 Dec 2010, Published online: 07 Feb 2011
 

Abstract

Animal data indicate that developmental tetrachlorodibenzo-p-dioxin exposure alters immune function; however, the potential immunotoxicity of dioxin-like and non-dioxin-like polychlorinated biphenyls (PCBs) in the developing infant is an understudied area. The aim of the current study is to examine the association between maternal and early postnatal PCB concentrations in relation to total infant serum immunoglobulin concentrations determined at 6-months-of-age. We selected 384 mother-infant pairs participating in a birth cohort study in Eastern Slovakia. PCB concentrations of several congeners were determined in maternal and cord serum samples and in infant serum samples collected at 6-months-of-age using gas chromatography with electron capture detection. Total immunoglobulin (Ig) G, A, and M concentrations were determined by nephelometry, and IgE concentrations were determined by enzyme-linked immunoassay. Linear regression models with adjustment for potential confounding factors were used to estimate the associations between maternal, cord, and 6-month infant PCB concentrations and total serum immunoglobulins. The median maternal serum concentration of PCB-153 was 140 ng/g lipid, ≈10-fold higher than concentrations in childbearing-age women in the United States during the same period. Maternal, cord, or 6-month infant PCB concentrations were not associated with total serum immunoglobulin levels at 6 months, regardless of the timing of PCB exposure, PCB congener, or specific immunoglobulin. In this population, which has high PCB concentrations relative to most populations in the world today, we did not observe any association between maternal and early postnatal PCB concentrations and total immunoglobulin measures of IgG, IgA, IgM, or IgE.

Acknowledgements

The authors wish to thank Drs. Allen Silverstone and Troy Torgerson for helpful discussions about the developing immune system, and Jan Petrik, Zhiwei Yu, and Hye-Youn Park who was each instrumental in getting the early parts of this project organized.

Declaration of interest

This research received support from National Institutes of Health grants T32-ES007262, T32-RR023256, U01-ES016127, and R01-CA096525 and from the Intramural Research Program of the National Institutes of Health, National Institute of Environmental Health Sciences. Support was also provided by a dissertation award from the University of Washington Department of Epidemiology and a Fulbright Grant from the US State Department.

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