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Updated: May 3, 2026

Modeling Ascending Vaginal Infection, Preterm Birth, and Neonatal Morbidity in Mice
Published on: October 10, 2025
Mouse model of intrauterine inflammation: sex-specific differences in long-term neurologic and immune sequelae
Tahani Dada1, Jason M Rosenzweig1, Mofeedah Al Shammary1
1Integrated Research Center for Fetal Medicine, Department of Gynecology and Obstetrics, Johns Hopkins University School of Medicine, Baltimore, MD, United States.
Insights
Prenatal inflammation in preterm infants can cause long-term neurological issues, including behavioral and motor disabilities. This study reveals chronic brain inflammation and sex-specific differences in offspring development.
Area of Science:
- Neuroscience
- Developmental Biology
- Immunology
Background:
- Preterm infants exposed to intrauterine infection/inflammation face high risks of neurological deficits.
- Previous research demonstrated acute fetal brain injury from intrauterine inflammation in a mouse model.
Purpose of the Study:
- To investigate long-term neurological outcomes into adulthood following prenatal inflammation.
- To identify sex-specific differences in brain development and neurological sequelae.
Main Methods:
- Neurobehavioral assessments
- Magnetic Resonance Imaging (MRI)
- Immunohistochemistry
- Flow cytometry for immune cells
Main Results:
- Prenatal inflammation induced lasting changes in MRI and behavior from neonate to adult stages.
- Chronic brain inflammation, including microglial activation and macrophage infiltration, led to neuronal loss.
- Significant sex-specific differences were observed in the long-term neurological consequences.
Conclusions:
- Intrauterine inflammation during early development leads to persistent neuroinflammation and neuronal damage.
- The study highlights critical sex-specific vulnerabilities in neurological development following prenatal inflammatory insults.
Abstract:
Preterm infants, especially those that are exposed to prenatal intrauterine infection or inflammation, are at a major risk for adverse neurological outcomes, including cognitive, motor and behavioral disabilities. We have previously shown in a mouse model that there is an acute fetal brain insult associated with intrauterine inflammation. The objectives of this study were: (1) to elucidate long-term (into adolescence and adulthood) neurological outcomes by assessing neurobehavioral development, MRI, immunohistochemistry and flow cytometry of cells of immune origin and (2) to determine whether there are any sex-specific differences in brain development associated with intrauterine inflammation. Our results have shown that prenatal exposure appeared to lead to changes in MRI and behavior patterns throughout the neonatal period and during adulthood. Furthermore, we observed chronic brain inflammation in the offspring, with persistence of microglial activation and increased numbers of macrophages in the brain, ultimately resulting in neuronal loss. Moreover, our study highlights the sex-specific differences in long-term sequelae. This study, while extending the growing literature of adverse neurologic outcomes following exposure to inflammation during early development, presents novel findings in the context of intrauterine inflammation.
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