Evidence map›Paper›PMID 31729416›Full record

ArticleScientific reports2019

Maternal and early postnatal immune activation produce sex-specific effects on autism-like behaviors and neuroimmune function in mice.

William A Carlezon, Woori Kim, Galen Missig, Beate C Finger, Samantha M Landino, Abigail J Alexander, Emery L Mokler, James O Robbins, Yan Li, Vadim Y Bolshakov and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 87 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
87citing papers in PubMed, 1 pooled it
20.0field-weighted citation impact, top 1% of its field
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

87 citing papers in PubMed, 1 synthesis or guideline pooled it, 142 citations in OpenAlex.

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27 more citing papers are in PubMed but not listed here.

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

12 authors at 1 institution in 1 country.

William A CarlezonBasic Neuroscience Division, Harvard Medical School, McLean Hospital, Belmont, MA, USA. bcarlezon@mclean.harvard.edu.
Woori KimBasic Neuroscience Division, Harvard Medical School, McLean Hospital, Belmont, MA, USA.
Galen MissigBasic Neuroscience Division, Harvard Medical School, McLean Hospital, Belmont, MA, USA.ORCID http://orcid.org/0000-0001-9026-9342
Beate C FingerBasic Neuroscience Division, Harvard Medical School, McLean Hospital, Belmont, MA, USA.
Samantha M LandinoBasic Neuroscience Division, Harvard Medical School, McLean Hospital, Belmont, MA, USA.
Abigail J AlexanderBasic Neuroscience Division, Harvard Medical School, McLean Hospital, Belmont, MA, USA.
Emery L MoklerBasic Neuroscience Division, Harvard Medical School, McLean Hospital, Belmont, MA, USA.
James O RobbinsBasic Neuroscience Division, Harvard Medical School, McLean Hospital, Belmont, MA, USA.
Yan LiBasic Neuroscience Division, Harvard Medical School, McLean Hospital, Belmont, MA, USA.ORCID http://orcid.org/0000-0003-3673-181X
Vadim Y BolshakovBasic Neuroscience Division, Harvard Medical School, McLean Hospital, Belmont, MA, USA.
Christopher J McDougleLurie Center for Autism, Harvard Medical School, Massachusetts General Hospital, Lexington, MA, USA.
Kwang-Soo KimBasic Neuroscience Division, Harvard Medical School, McLean Hospital, Belmont, MA, USA. kskim@mclean.harvard.edu.
Harvard University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Increasing evidence suggests a role for inflammation in neuropsychiatric conditions including autism spectrum disorder (ASD), a neurodevelopmental syndrome with higher prevalence in males than females. Here we examined the effects of early-life immune system activation (EIA)-comprising regimens of prenatal, early postnatal, or combined ("two-hit") immune activation-on the core behavioral features of ASD (decreased social interaction, increased repetitive behavior, and aberrant communication) in C57BL/6J mice. We treated timed-pregnant mice with polyinosinic:polycytidylic acid (Poly I:C) on gestational day 12.5 to produce maternal immune activation (MIA). Some offspring also received lipopolysaccharide (LPS) on postnatal day 9 to produce postnatal immune activation (PIA). EIA produced disruptions in social behavior and increases in repetitive behaviors that were larger in males than in females. Ultrasonic vocalizations (USVs) were altered in both sexes. Molecular studies revealed that EIA also produced prominent sex-specific changes in inflammation-related gene expression in the brain. Whereas both sexes showed increases in pro-inflammatory factors, as reflected by levels of mRNA and protein, expression of anti-inflammatory factors was decreased in males but increased in females. Our findings demonstrate that EIA can produce sex-specific behavioral effects and immune responses in the brain, and identify molecular processes that may contribute to resilience in females.

Indexed as

ImmunityNeuroimmunomodulationPrenatal Exposure Delayed EffectsAnimalsAutistic DisorderBehavior, AnimalBiomarkersCytokinesDisease Models, AnimalDisease SusceptibilityFemaleGene ExpressionInflammation MediatorsMaleMaternal ExposureMiceBiomarkersCytokinesInflammation Mediators

Identifiers

PMID31729416
PMCPMC6858355
OpenAlexW2983956737

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.