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Cord blood T cell subpopulations and associations with maternal cadmium and arsenic exposures.

Authors :
Nygaard UC
Li Z
Palys T
Jackson B
Subbiah M
Malipatlolla M
Sampath V
Maecker H
Karagas MR
Nadeau KC
Source :
PloS one [PLoS One] 2017 Jun 29; Vol. 12 (6), pp. e0179606. Date of Electronic Publication: 2017 Jun 29 (Print Publication: 2017).
Publication Year :
2017

Abstract

Background: Arsenic and cadmium are environmental pollutants, and although the evidence for adverse immune effects after prenatal arsenic and cadmium exposures is increasing, little is known about the underlying immunological mechanisms.<br />Methods: We investigated the relationship between prenatal arsenic and cadmium exposures and a variety of T cell subpopulations measured in cord blood for 63 participants in the New Hampshire Birth Cohort Study. Post-partum toenail concentrations of arsenic and cadmium were used as an estimate of maternal exposure during pregnancy. The characteristics of cord blood proportions of T lymphocytes and subpopulations (expression of markers for Th1, Th2, Th17, Th1Th17, induced and natural regulatory T cells and NKTs) are presented.<br />Results: In regression analyses, maternal arsenic exposure levels were inversely associated with cord blood T helper memory cells (-21%, 95% CI: -36%, -3%) and the association was found to be stronger in females. They were also inversely associated with activated T helper memory cells, particularly in males (-26%, 95% CI: -43%, -3%). Similarly, inverse associations were observed between cadmium exposure levels and activated T helper memory cells (-16%, 95% CI: -30%, -1%) and also for T helper memory cells in females (-20%, 95% CI: -35%, -3%).<br />Conclusion: The results suggest that prenatal exposures to relatively low levels of arsenic and cadmium may contribute to altered distribution of T cell populations at birth. These changes in theory, could have contributed to the previously reported immunosuppressive effects observed later in infancy/childhood.

Details

Language :
English
ISSN :
1932-6203
Volume :
12
Issue :
6
Database :
MEDLINE
Journal :
PloS one
Publication Type :
Academic Journal
Accession number :
28662050
Full Text :
https://doi.org/10.1371/journal.pone.0179606