Evidence map›Paper›PMID 28485733›Full record

ArticleTranslational psychiatry2017

Maternal immune activation results in complex microglial transcriptome signature in the adult offspring that is reversed by minocycline treatment.

D Mattei, A Ivanov, C Ferrai, P Jordan, D Guneykaya, A Buonfiglioli, W Schaafsma, P Przanowski, W Deuther-Conrad, P Brust and 11 more

Open access · goldAbstract read
In one paragraph

Article in Translational psychiatry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 131 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
131citing papers in PubMed, 3 pooled it
12.2field-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

131 citing papers in PubMed, 3 syntheses or guidelines pooled it, 215 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Review
  5. Review
  6. A Developmental Neuroimmune Cascade Model of Autism Spectrum Disorder.International journal of molecular sciences · 2026
    Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Immune dysfunction in Alzheimer disease.Nature reviews. Neuroscience · 2026
    Review
  12. Article
  13. Microglia as critical mediators linking perinatal immune stress to mental health trajectories.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Review
  14. Review
  15. Review
  16. Article
  17. Review
  18. Microglial plasticity across development mediates infantile amnesia.bioRxiv : the preprint server for biology · 2025
    Article
  19. Review
  20. Review

71 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

21 authors at 8 institutions in 3 countries.

D MatteiCellular Neurocience, Max-Delbrueck-Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany.
A IvanovCore Unit Bioinformatics, Berlin Institute of Health, Berlin, Germany.
C FerraiEpigenetic Regulation and Chromatin Architecture Group, Berlin Institute for Medical Systems Biology, Max-Delbrück Centre for Molecular Medicine in the Helmholtz Association, Berlin, Germany.
P JordanCellular Neurocience, Max-Delbrueck-Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany.
D GuneykayaCellular Neurocience, Max-Delbrueck-Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany.
A BuonfiglioliCellular Neurocience, Max-Delbrueck-Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany.
W SchaafsmaDepartment of Neuroscience, Section Medical Physiology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
P PrzanowskiLaboratory of Molecular Neurobiology, Nencki Institute of Experimental Biology, Warsaw, Poland.
W Deuther-ConradDepartment of Neuroradiopharmaceuticals, Institute of Radiopharmaceutical Cancer Research, Research Site Leipzig, Helmholtz-Zentrum Dresden-Rossendorf, Leipzig, Germany.
P BrustDepartment of Neuroradiopharmaceuticals, Institute of Radiopharmaceutical Cancer Research, Research Site Leipzig, Helmholtz-Zentrum Dresden-Rossendorf, Leipzig, Germany.
S HesseDepartment of Nuclear Medicine, University of Leipzig, Leipzig, Germany.
M PattDepartment of Nuclear Medicine, University of Leipzig, Leipzig, Germany.
O SabriDepartment of Nuclear Medicine, University of Leipzig, Leipzig, Germany.
T L RossDepartment of Nuclear Medicine, Hannover Medical School, Hannover, Germany.
B J L EggenDepartment of Neuroscience, Section Medical Physiology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
E W G M BoddekeDepartment of Neuroscience, Section Medical Physiology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
B KaminskaLaboratory of Molecular Neurobiology, Nencki Institute of Experimental Biology, Warsaw, Poland.
D BeuleCore Unit Bioinformatics, Berlin Institute of Health, Berlin, Germany.
A PomboEpigenetic Regulation and Chromatin Architecture Group, Berlin Institute for Medical Systems Biology, Max-Delbrück Centre for Molecular Medicine in the Helmholtz Association, Berlin, Germany.
H KettenmannCellular Neurocience, Max-Delbrueck-Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany.
S A WolfCellular Neurocience, Max-Delbrueck-Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany.
Max Delbrück Center · DEUniversity of Groningen · NLBerlin Institute of Health at Charité - Universitätsmedizin Berlin · DEHelmholtz-Zentrum Dresden-Rossendorf · DEInstytut Biologii Doświadczalnej im. Marcelego Nenckiego · PLLeipzig University · DEIFB Adiposity Diseases · DEMedizinische Hochschule Hannover · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Maternal immune activation (MIA) during pregnancy has been linked to an increased risk of developing psychiatric pathologies in later life. This link may be bridged by a defective microglial phenotype in the offspring induced by MIA, as microglia have key roles in the development and maintenance of neuronal signaling in the central nervous system. The beneficial effects of the immunomodulatory treatment with minocycline on schizophrenic patients are consistent with this hypothesis. Using the MIA mouse model, we found an altered microglial transcriptome and phagocytic function in the adult offspring accompanied by behavioral abnormalities. The changes in microglial phagocytosis on a functional and transcriptional level were similar to those observed in a mouse model of Alzheimer's disease hinting to a related microglial phenotype in neurodegenerative and psychiatric disorders. Minocycline treatment of adult MIA offspring reverted completely the transcriptional, functional and behavioral deficits, highlighting the potential benefits of therapeutic targeting of microglia in psychiatric disorders.

Indexed as

Adult ChildrenAlzheimer DiseaseAnimalsAnti-Bacterial AgentsBehavior, AnimalDisease Models, AnimalFemaleHumansImmune System PhenomenaMiceMice, Inbred C57BLMicrogliaMinocyclinePhagocytosisPregnancySchizophreniaAnti-Bacterial AgentsMinocycline

Identifiers

PMID28485733
PMCPMC5534948
OpenAlexW2613880574

What OpenQuestion holds

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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.