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Published on: August 7, 2017
Early life exposure to air pollution and cell-mediated immune responses in preschoolers
Yan-Ling Deng1, Jia-Qiang Liao2, Bin Zhou3
1Department of Occupational and Environmental Health, School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, PR China; Key Laboratory of Environment and Health, Ministry of Education & Ministry of Environmental Protection, and State Key Laboratory of Environmental Health (incubating), School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, PR China.
Insights
Prenatal and postnatal exposure to air pollution impacts preschoolers' immune systems, with effects varying by exposure timing and child's sex. This research highlights critical windows for air pollution's influence on developing immune function.
Area of Science:
- Environmental Health
- Immunology
- Pediatrics
Background:
- Air pollution exposure is linked to immune dysfunction in adults.
- Limited understanding exists regarding air pollution's impact on early-life immune development.
- This study addresses the effects of prenatal and postnatal air pollution on preschooler immune function.
Purpose of the Study:
- To investigate the association between prenatal and postnatal air pollution exposure and cell-mediated immune function in preschoolers.
- To identify critical windows of exposure during early development.
- To explore potential sex-specific differences in immune responses.
Main Methods:
- Recruited 391 preschoolers from a mother-child cohort in Wuhan, China.
- Utilized a land use regression (LUR) model to estimate exposure to PM2.5, PM10, and NO2 during pregnancy and early childhood.
- Assessed cell-mediated immunity through peripheral blood T lymphocyte subsets and plasma cytokines.
Main Results:
- Prenatal exposure to PM2.5, PM10, and NO2 in early pregnancy was linked to decreased CD3+ and CD3+CD8+ cells.
- Late prenatal exposure showed a positive association with CD3+ cells.
- Postnatal exposures were positively associated with increased levels of IL-4, IL-5, IL-6, and TNF-α.
- Immune response variations were observed based on the child's sex.
Conclusions:
- Air pollution exposure during different developmental stages in early life differentially affects cellular immune responses.
- The observed effects of air pollution on immune function appear to be sex-specific.
- Findings underscore the importance of mitigating air pollution exposure during critical prenatal and postnatal periods.
Background:
Exposure to air pollution has been linked with altered immune function in adults, but little is known about its effects on early life. This study aimed to investigate the effects of exposure to air pollution during prenatal and postnatal windows on cell-mediated immune function in preschoolers.
Methods:
Pre-school aged children (2.9 ± 0.5 y old, n = 391) were recruited from a mother-child cohort study in Wuhan, China. We used a spatial-temporal land use regression (LUR) model to estimate exposures of particulate matter with aerodynamic diameters ≤2.5 μm (PM2.5) and ≤10 μm (PM10), and nitrogen dioxide (NO2) during the specific trimesters of pregnancy and the first two postnatal years. We measured peripheral blood T lymphocyte subsets and plasma cytokines as indicators of cellular immune function. We used multiple informant models to examine the associations of prenatal and postnatal exposures to air pollution with cell-mediated immune function.
Results:
Prenatal exposures to PM2.5, PM10, and NO2 during early pregnancy were negatively associated with %CD3+ and %CD3+CD8+ cells, and during late pregnancy were positively associated with %CD3+ cells. Postnatal exposures to these air pollutants during 1-y or 2-y childhood were positively associated with IL-4, IL-5, IL-6, and TNF-α. We also observed that the associations of prenatal or postnatal air pollution exposures with cellular immune responses varied by child's sex.
Conclusions:
Our results suggest that exposure to air pollution during different critical windows of early life may differentially alter cellular immune responses, and these effects appear to be sex-specific.
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