Evidence map›Paper›PMID 26822608›Full record

ArticleScience (New York, N.Y.)2016

The maternal interleukin-17a pathway in mice promotes autism-like phenotypes in offspring.

Gloria B Choi, Yeong S Yim, Helen Wong, Sangdoo Kim, Hyunju Kim, Sangwon V Kim, Charles A Hoeffer, Dan R Littman, Jun R Huh

Open access · greenAbstract read
In one paragraph

Article in Science (New York, N.Y.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 723 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
723citing papers in PubMed, 2 pooled it
46.3field-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

723 citing papers in PubMed, 2 syntheses or guidelines pooled it, 1,217 citations in OpenAlex.

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Gloria B ChoiThe McGovern Institute for Brain Research, Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Yeong S YimThe McGovern Institute for Brain Research, Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Helen WongCenter for Neural Science, New York University, New York, NY 10003, USA. Institute for Behavioral Genetics, Department of Integrated Physiology, University of Colorado, Boulder, CO 80303, USA.
Sangdoo KimDivision of Infectious Diseases and Immunology and Program in Innate Immunity, Department of Medicine, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Hyunju KimDivision of Infectious Diseases and Immunology and Program in Innate Immunity, Department of Medicine, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Sangwon V KimThe Kimmel Center for Biology and Medicine of the Skirball Institute, New York University School of Medicine, New York, NY 10016, USA.
Charles A HoefferCenter for Neural Science, New York University, New York, NY 10003, USA. Institute for Behavioral Genetics, Department of Integrated Physiology, University of Colorado, Boulder, CO 80303, USA. charles.hoeffer@colorado.edu dan.littman@med.nyu.edu jun.huh@umassmed.edu.
Dan R LittmanThe Kimmel Center for Biology and Medicine of the Skirball Institute, New York University School of Medicine, New York, NY 10016, USA. Howard Hughes Medical Institute, New York, NY 10016, USA. charles.hoeffer@colorado.edu dan.littman@med.nyu.edu jun.huh@umassmed.edu.
Jun R HuhDivision of Infectious Diseases and Immunology and Program in Innate Immunity, Department of Medicine, University of Massachusetts Medical School, Worcester, MA 01605, USA. The Kimmel Center for Biology and Medicine of the Skirball Institute, New York University School of Medicine, New York, NY 10016, USA. charles.hoeffer@colorado.edu dan.littman@med.nyu.edu jun.huh@umassmed.edu.
New York University · USUniversity of Massachusetts Chan Medical School · USHoward Hughes Medical Institute · US

Funding

Training Program in Immunology and Inflammation.T32AI100853 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Susan Ruth Schwab · 2012 to 2026
$4.5M
Delineating the Anatomical and Functional Circuitry Underlying Social LearningR01MH106497 · NIMH · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI CHOI, GLORIA · 2015 to 2019
$2.0M
Akt regulation of synaptic plasticity and behaviorR01NS086933 · NINDS · UNIVERSITY OF COLORADO · PI HOEFFER, CHARLES A · 2015 to 2019
$1.8M
Chemical and genetic studies of RORgamma and its critical roles in IBDR00DK091508 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI HUH, JUN R. · 2013 to 2015
$747k
Non-canonical translation in hippocampal mGluR-dependent long-term depression - RF31NS083277 · NINDS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI WONG, HELEN · 2013 to 2014
$85k
Howard Hughes Medical InstituteNIAID NIH HHS T32 AI100853NIDDK NIH HHS R00 DK091508NIDDK NIH HHS R00DK091508NIMH NIH HHS R01 MH106497NINDS NIH HHS F31 NS083277NINDS NIH HHS F31NS083277NINDS NIH HHS R01 NS086933NINDS NIH HHS R01NS086933
6 · The paper itself

Abstract

Viral infection during pregnancy has been correlated with increased frequency of autism spectrum disorder (ASD) in offspring. This observation has been modeled in rodents subjected to maternal immune activation (MIA). The immune cell populations critical in the MIA model have not been identified. Using both genetic mutants and blocking antibodies in mice, we show that retinoic acid receptor-related orphan nuclear receptor gamma t (RORγt)-dependent effector T lymphocytes [for example, T helper 17 (TH17) cells] and the effector cytokine interleukin-17a (IL-17a) are required in mothers for MIA-induced behavioral abnormalities in offspring. We find that MIA induces an abnormal cortical phenotype, which is also dependent on maternal IL-17a, in the fetal brain. Our data suggest that therapeutic targeting of TH17 cells in susceptible pregnant mothers may reduce the likelihood of bearing children with inflammation-induced ASD-like phenotypes.

Indexed as

AnimalsAntibodies, BlockingAutism Spectrum DisorderBehavioral SymptomsBehavior, AnimalCerebral CortexFemaleInterleukin-17MaleMaternal-Fetal ExchangeMiceMutationNuclear Receptor Subfamily 1, Group F, Member 3PhenotypePregnancyPrenatal Exposure Delayed EffectsAntibodies, BlockingIl17a protein, mouseInterleukin-17Nuclear Receptor Subfamily 1, Group F, Member 3Receptors, Retinoic AcidRetinoic Acid Receptor gammaRNA, Messenger

Identifiers

PMID26822608
PMCPMC4782964
OpenAlexW2253802357

What OpenQuestion holds

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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.