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Prenatal stress has pro-inflammatory consequences on the immune system in adult rats
Christel C A Vanbesien-Mailliot1, Isabelle Wolowczuk, Jérôme Mairesse
1Perinatal Stress Unit, University Lille 1, F-59655 Villeneuve d'Ascq, France.
Insights
Prenatal stress (PS) in rats leads to long-lasting immune system changes. Adult offspring show heightened cellular immunity and inflammation, indicating increased disease vulnerability.
Area of Science:
- Immunology
- Developmental Biology
- Neuroscience
Background:
- The prenatal environment significantly influences offspring immune system development.
- Adverse early life experiences, like prenatal stress, may increase disease susceptibility.
- Limited understanding exists regarding the specific impacts of prenatal stress on immune ontogeny.
Purpose of the Study:
- To investigate the effects of restraint prenatal stress (PS) on cellular and humoral immunity in male rat offspring.
- To assess immune responsiveness in vitro and in vivo at different developmental stages (7 weeks and 6 months).
Main Methods:
- Exposure of pregnant rats to restraint stress.
- Assessment of immune cell populations (CD8+, NK cells) and cytokine mRNA expression (IFN-gamma) in offspring.
- In vitro lymphocyte proliferation and cytokine secretion assays.
- In vivo IFN-gamma neutralization in young rats.
Main Results:
- Adult (6-month-old) PS rats exhibited increased circulating CD8+ and NK cells, with elevated IFN-gamma mRNA.
- In vitro stimulation revealed enhanced T lymphocyte proliferation and IFN-gamma secretion in adult PS rats.
- Young (7-week-old) PS rats showed only a minor increase in pro-inflammatory cytokine mRNA; in vivo IFN-gamma neutralization had no effect.
- These findings suggest age-dependent immune alterations following prenatal stress.
Conclusions:
- Prenatal stress induces long-lasting pro-inflammatory effects on the immune system in male rats.
- The immune system's response to prenatal stress is age-dependent, with more pronounced effects observed in adulthood.
- This study highlights the critical role of the prenatal environment in shaping long-term immune health and disease risk.
Abstract:
The in utero environment is critical for initiating the ontogeny of several physiological systems, including the immune surveillance. Yet, little is known about adverse early experiences on the offspring's immunity and vulnerability to disease. The present work aimed at investigating the impact of restraint prenatal stress (PS) on the development and responsiveness of in vitro and in vivo cellular and humoral immunity of male progeny aged 7 weeks and 6 months. In adult 6-month-old rats, we detected increased circulating CD8(+)-expressing and NK cells in PS rats as compared to controls, associated with higher mRNA expression of IFN-gamma. In addition, in vitro stimulation with phytohemagglutinin-A induced an increase in both the proliferation of T lymphocytes and the secretion of IFN-gamma in PS rats. Interestingly, these alterations were undetectable in younger PS rats (7-week old), except for a slight increase in the mRNA expression of several pro-inflammatory cytokines in peripheral blood mononuclear cells. Moreover, in vivo neutralization of IFN-gamma in young rats had no effects in PS group. In conclusion, we report for the first time long-lasting pro-inflammatory consequences of PS in rats.
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