Evidence map›Paper›PMID 32879327›Full record

ArticleScientific reports2020

In utero exposure to endogenous maternal polyclonal anti-Caspr2 antibody leads to behavioral abnormalities resembling autism spectrum disorder in male mice.

Ciara Bagnall-Moreau, Patricio T Huerta, Davide Comoletti, Andrea La-Bella, Roseann Berlin, Chunfang Zhao, Bruce T Volpe, Betty Diamond, Lior Brimberg

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

15 citing papers in PubMed, 20 citations in OpenAlex.

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  14. Autoantibody-associated psychiatric syndromes in children: link to adult psychiatry.Journal of neural transmission (Vienna, Austria : 1996) · 2021
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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

9 authors at 2 institutions in 2 countries.

Ciara Bagnall-MoreauCenter for Autoimmune Musculoskeletal and Hematopoietic Diseases, Institute of Molecular Medicine, Feinstein Institutes for Medical Research, 350 Community Drive, Manhasset, NY, 11030, USA.
Patricio T HuertaLaboratory of Immune and Neural Networks, Institute of Molecular Medicine, Feinstein Institutes for Medical Research, Manhasset, USA.
Davide ComolettiDepartments of Neuroscience and Cell Biology Robert Wood Johnson Medical School, Rutgers, The State University of New Jersey, New Brunswick, NJ, 08901, USA.
Andrea La-BellaCenter for Autoimmune Musculoskeletal and Hematopoietic Diseases, Institute of Molecular Medicine, Feinstein Institutes for Medical Research, 350 Community Drive, Manhasset, NY, 11030, USA.
Roseann BerlinLaboratory of Functional Neuroanatomy, Institute of Molecular Medicine, Feinstein Institutes for Medical Research, Manhasset, USA.
Chunfang ZhaoCenter for Autoimmune Musculoskeletal and Hematopoietic Diseases, Institute of Molecular Medicine, Feinstein Institutes for Medical Research, 350 Community Drive, Manhasset, NY, 11030, USA.
Bruce T VolpeLaboratory of Functional Neuroanatomy, Institute of Molecular Medicine, Feinstein Institutes for Medical Research, Manhasset, USA.
Betty DiamondCenter for Autoimmune Musculoskeletal and Hematopoietic Diseases, Institute of Molecular Medicine, Feinstein Institutes for Medical Research, 350 Community Drive, Manhasset, NY, 11030, USA.
Lior BrimbergCenter for Autoimmune Musculoskeletal and Hematopoietic Diseases, Institute of Molecular Medicine, Feinstein Institutes for Medical Research, 350 Community Drive, Manhasset, NY, 11030, USA. lbrimberg@northwell.edu.
Feinstein Institute for Medical Research · USVictoria University of Wellington · NZ

Funding

A diagnostic for maternal autoAb to Caspr2 to predict increased risk of autism spectrum disorder in childrenR43HD092128 · NICHD · SPARK2FLAME, INC. · PI BURCH, RONALD M · 2017 to 2017
$220k
NICHD NIH HHS R43 HD092128
6 · The paper itself

Abstract

The concept that exposure in utero to maternal anti-brain antibodies contributes to the development of autism spectrum disorders (ASD) has been entertained for over a decade. We determined that antibodies targeting Caspr2 are present at high frequency in mothers with brain-reactive serology and a child with ASD, and further demonstrated that exposure in utero to a monoclonal anti-Caspr2 antibody, derived from a mother of an ASD child, led to an-ASD like phenotype in male offspring. Now we propose a new model to study the effects of in utero exposure to anti-Caspr2 antibody. Dams immunized with the extracellular portion of Caspr2 express anti-Caspr2 antibodies throughout gestation to better mimic the human condition. Male but not female mice born to dams harboring polyclonal anti-Caspr2 antibodies showed abnormal cortical development, decreased dendritic complexity of excitatory neurons and reduced numbers of inhibitory neurons in the hippocampus, as well as repetitive behaviors and impairments in novelty interest in the social preference test as adults. These data supporting the pathogenicity of anti-Caspr2 antibodies are consistent with the concept that anti-brain antibodies present in women during gestation can alter fetal brain development, and confirm that males are peculiarly susceptible.

Indexed as

AnimalsAntibodies, Anti-IdiotypicAutism Spectrum DisorderAutoantibodiesBehavior, AnimalBrainDisease Models, AnimalFemaleHippocampusHumansMaleMaternal-Fetal RelationsMaternal InheritanceMembrane ProteinsMiceNerve Tissue ProteinsAntibodies, Anti-IdiotypicAutoantibodiesCNTNAP2 protein, mouseMembrane ProteinsNerve Tissue Proteins

Identifiers

PMID32879327
PMCPMC7468145
OpenAlexW3082790201

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.