Evidence map›Paper›PMID 41973698›Full record

ArticleJournal of visualized experiments : JoVE2026

Generation of the Early-Gestational Maternal Immune Activation Mouse Model to Assess Prenatal Inflammation on Neurodevelopment.

Sydney Camfield, Abril Gaona-Gamboa, Clara L Hibbs, Lindsay N Hayes

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In one paragraph

Article in Journal of visualized experiments : JoVE, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Sydney CamfieldDepartment of Cell Biology, College of Medicine, University of Oklahoma.
Abril Gaona-GamboaGraduate Program in Neuroscience, College of Medicine, University of Oklahoma.
Clara L HibbsDepartment of Cell Biology, College of Medicine, University of Oklahoma.
Lindsay N HayesDepartment of Cell Biology, College of Medicine, University of Oklahoma; Graduate Program in Neuroscience, College of Medicine, University of Oklahoma; Lindsay-Hayes@ou.edu.

Funding

Vascular-macrophage crosstalk in GBM immunosuppressionP20GM134973 · NIGMS · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI Robyn Stacey Kent · 2020 to 2026
$17.6M
Learning and Achievement in Biomedical SciencesT32GM154645 · NIGMS · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI CHRISTOPHER G HORTON, ERIC W HOWARD · 2025 to 2026
$717k
Tracking myeloid heterogeneity in mouse models and cerebrospinal fluid of HIV-suppressed individuals to classify neuroinflammation and identify molecular markers associated with clinical pathologyK01AG087810 · NIA · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI Lindsay Nicole Hayes · 2024 to 2026
$396k
NIA NIH HHS K01 AG087810NIGMS NIH HHS P20 GM134973NIGMS NIH HHS T32 GM154645
6 · The paper itself

Abstract

Neurodevelopmental disorders (NDDs) arise from complex interactions between genetic and environmental risk factors, including prenatal immune activation. Maternal immune activation (MIA) in mice is a widely used model to study environmental contributions to NDDs; variability in experimental outcomes limits reproducibility. Here, we present a standardized protocol for inducing MIA during early gestation at embryonic day 9.5 (E9.5) in mice, incorporating multiple quality control metrics to assess immune response and predict pregnancy outcomes. Following administration of polyinosinic:polycytidylic acid (poly(I:C)), maternal serum cytokines are quantified to confirm robust immune activation, allowing an exclusion metric for low responders. Maternal weight trajectories from E0.5 to E12.5 are predictive of litter viability, with dams that produced litter exhibiting characteristic weight-gain patterns distinct from dams that lost a litter. We also observed that the animal vendor significantly influenced maternal immune response and litter viability, while poly(I:C) formulation was not a significant factor. Altogether, the protocol provides strategies to enhance the reproducibility of the early-gestational MIA model and the viability of the offspring by monitoring maternal immune response and weight changes, and by controlling animal vendors, to ultimately study the effect of prenatal immune activation on neurodevelopment.

Indexed as

Disease Models, AnimalInflammationNeurodevelopmental DisordersAnimalsCytokinesFemaleMiceNeurodevelopmentPoly I-CPregnancyCytokinesPoly I-C

Identifiers

PMID41973698
PMCPMC13674793

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.