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Published May 1, 2015 | Supplemental Material
Journal Article Open

Maternal Immune Activation in Nonhuman Primates Alters Social Attention in Juvenile Offspring

Abstract

BACKGROUND: Sickness during pregnancy is associated with an increased risk of offspring neurodevelopmental disorders. Rodent models have played a critical role in establishing causal relationships and identifying mechanisms of altered brain and behavior development in pups prenatally exposed to maternal immune activation (MIA). We recently developed a novel nonhuman primate model to bridge the gap between human epidemiological studies and rodent models of prenatal immune challenge. Our initial results demonstrated that rhesus monkeys given the viral mimic synthetic double-stranded RNA (polyinosinic:polycytidylic acid stabilized with poly-l-lysine) during pregnancy produce offspring with abnormal repetitive behaviors, altered communication, and atypical social interactions. METHODS: We utilized noninvasive infrared eye tracking to further evaluate social processing capabilities in a subset of the first trimester MIA-exposed offspring (n = 4) and control animals (n = 4) from our previous study. RESULTS: As juveniles, the MIA offspring differed from control animals on several measures of social attention, particularly when viewing macaque faces depicting the fear grimace facial expression. Compared with control animals, MIA offspring had a longer latency before fixating on the eyes, had fewer fixations directed at the eyes, and spent less total time fixating on the eyes of the fear grimace images. CONCLUSIONS: In the rhesus monkey model, exposure to MIA at the end of the first trimester results in abnormal gaze patterns to salient social information. The use of noninvasive eye tracking extends the findings from rodent MIA models to more human-like behaviors resembling those in both autism spectrum disorder and schizophrenia.

Additional Information

© 2014 Society of Biological Psychiatry. This work was supported by a grant from the Simons Foundation (SFARI 9900060 to PHP) and by a gift from Ted and Ginger Jenkins. Additional support was provided by the Center for Neuroscience at the University of California, Davis, and the base grant (RR00169) of the California National Primate Research Center. SEPS is currently affiliated with Department of Immunology, Mayo Clinic, Rochester, Minnesota. We thank the veterinary and animal services staff of the California National Primate Research Center for helping to refine the animal handling procedures described in this article. We also thank the four anonymous reviewers that provided positive and constructive comments on an earlier version of this paper. Poly-ICLC was kindly provided by Dr. Andres Salazar, M.D., Oncovir, Washington, DC. The authors report no biomedical financial interests or potential conflicts of interest.

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August 22, 2023
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