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Published on: March 6, 2018
The kinetics of cell surface receptor expression in children perinatally exposed to polychlorinated biphenyls
M Horváthová1, E Jahnová, L Palkovičová
1Department of Immunology and Immunotoxicology, Slovak Medical University, Bratislava, Slovakia. mira.horvathova@szu.sk
Insights
Early life exposure to polychlorinated biphenyls (PCBs) significantly alters immune cell development. Infants in high-PCB areas showed altered T-lymphocyte and dendritic cell populations, indicating impaired immune system development.
Area of Science:
- Immunology
- Environmental Health
- Developmental Biology
Background:
- Polychlorinated biphenyls (PCBs) are environmental contaminants known to disrupt normal development.
- Prenatal and early postnatal exposure to PCBs can impact immune system maturation.
- Understanding these effects is crucial for public health, especially in contaminated regions.
Purpose of the Study:
- To investigate the impact of environmental PCB contamination on immune cell development in infants.
- To evaluate differences in lymphocyte and dendritic cell populations between high and low PCB exposure areas.
- To assess the correlation between PCB exposure levels and specific immune cell markers.
Main Methods:
- Blood samples collected from newborns, 6-month-olds, and 16-month-olds in high (Michalovce) and low (Svidnik/Stropkov) PCB contamination districts.
- Multi-color flow cytometry used to analyze lymphocyte receptor expression.
- Statistical analysis, including multivariate models, adjusted for covariates like maternal age, parity, and breastfeeding.
Main Results:
- Infants in the high PCB area (Michalovce) showed increased lymphoid dendritic cells (DC) and naïve/resting T-lymphocytes at 6 months.
- Reduced natural regulatory T-lymphocytes and suppressor inducer T-lymphocytes were observed in the high PCB area.
- Significant differences in memory T-lymphocytes, TEM T-lymphocytes, and myeloid DC persisted between districts after covariate adjustment.
Conclusions:
- Prenatal and early postnatal PCB exposure significantly affects the dynamics of cell surface receptor expression on immune cells.
- These alterations suggest impaired immunologic development in infants exposed to higher levels of PCBs.
- The findings highlight the long-term health risks associated with environmental PCB contamination during critical developmental windows.
Abstract:
Exposure to polychlorinated biphenyls (PCBs) during pre-natal and early life can alter normal immune system development. Blood specimens from newborns, 6-, and 16-month-old infants were collected in the Michalovce and Svidnik/Stropkov districts, areas with, respectively, high and low environmental PCB contamination, and lymphocyte receptor expression was evaluated by multi-color flow cytometry. The results indicate that the percentage of lymphoid dendritic cells (DC) and naïve/resting T-lymphocytes were significantly increased at 6-months in Michalovce as compared to the same cell types in cord blood samples (p < 0.001), whereas natural regulatory T-lymphocytes and suppressor inducer T-lymphocytes were reduced (p < 0.001). Overall, a positive linear correlation of terminally differentiated effector memory (TEM) T-lymphocyte population with age, but a negative linear correlation for myeloid DC from birth to 6-months in both regions were found. Michalovce samples indicated significantly higher expression of memory T-lymphocytes (birth, 6(th), and 16(th) month), TEM T-lymphocytes (birth and 6(th) month), and lymphoid DC (6(th) month) compared to the Svidnik/Stropkov regions. After adjustment for relevant covariates, such as maternal age, parity, season of birth, breastfeeding, birth weight, and gender, the myeloid DC, suppressor inducer T-lymphocytes, truly naïve helper/inducer T-lymphocytes, and TEM T-lymphocytes remained significantly different between districts in cord blood samples. The multivariate analysis models for 6- and 16-month samples showed district differences in all cellular determinants, except for lymphoid DC and macrophage-like cells. This study provides the first evidence that pre-natal and early post-natal exposure to PCBs affects the dynamics of cell surface receptor expression on lymphoid DC and DC-like cells, suggesting impaired immunologic development following pre-natal and early post-natal PCB exposure.
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