Evidence map›Paper›PMID 20371618›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2010

CNS expression of anti-inflammatory cytokine interleukin-4 attenuates Alzheimer's disease-like pathogenesis in APP+PS1 bigenic mice.

Tomomi Kiyota, Satoshi Okuyama, Russell J Swan, Michael T Jacobsen, Howard E Gendelman, Tsuneya Ikezu

Open access · greenAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 121 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
121citing papers in PubMed, 2 pooled it
6.2field-weighted citation impact, top 3% 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

121 citing papers in PubMed, 2 syntheses or guidelines pooled it, 208 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Review
  5. Article
  6. Review
  7. Review
  8. Brain interleukins and Alzheimer's disease.Metabolic brain disease · 2025
    Review
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  10. Article
  11. Review
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  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Type 2 immunity in the brain and brain borders.Cellular & molecular immunology · 2023
    Review
  20. Article

61 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

6 authors at 1 institution in 1 country.

Tomomi KiyotaDepartment of Pharmacology and Experimental Neuroscience, Nebraska Medical Center, Omaha, NE 68198, USA.
Satoshi Okuyama
Russell J Swan
Michael T Jacobsen
Howard E Gendelman
Tsuneya Ikezu
University of Nebraska Medical Center · US

Funding

Proteomics CoreP01NS043985 · NINDS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI ZHENG, JIALIN CHARLES · 2003 to 2012
$11.8M
In Vivo Reconstitution Models for NeuroAIDS and Beta-AmyloidosisR01MH083523 · NIMH · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI IKEZU, TSUNEYA · 2009 to 2010
$765k
Anti-inflammatory regulation of beta-amyloidosisR21AG032600 · NIA · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI IKEZU, TSUNEYA · 2009 to 2010
$346k
NIA NIH HHS R21 AG032600NIMH NIH HHS R01 MH083523NINDS NIH HHS P01 NS043985
6 · The paper itself

Abstract

Cytokines play an emerging role as neurotransmitters, neuromodulators, and neurohormones in the brain. This paradigm shift in cytokine function offers a new framework to understand their roles in ameliorating neurodegenerative disorders, such as Alzheimer's disease (AD). Molecular adjuvant therapy of AD animal models with glatiramer acetate induces anti-inflammatory responses and therapeutic effects. Although these effects are potentially mediated through anti-inflammatory cytokine signaling, the exact molecular identities and pathways are poorly understood. Here, we show that virus-mediated expression of the mouse interleukin (IL)-4 gene in beta-amyloid precursor protein + presenilin-1 (APP+PS1) bigenic mice attenuates AD pathogenesis. Introduction of an adeno-associated viral (AAV) vector encoding IL-4 into the hippocampus resulted in sustained expression of IL-4, reduced astro/microgliosis, amyloid-beta peptide (Abeta) oligomerization and deposition, and enhanced neurogenesis. Moreover, increased levels of IL-4 improved spatial learning, promoted phosphorylation of N-methyl-D-aspartate receptor subunit 2B at Tyr 1472, and enhanced its cell surface retention both in vivo and in vitro. Our data suggest that neuronal anti-inflammatory cytokine signaling may be a potential alternative target for non-Abeta-mediated treatment of AD.

Indexed as

Alzheimer DiseaseAmyloid beta-Protein PrecursorAnimalsAnti-Inflammatory AgentsCentral Nervous SystemGenetic TherapyHippocampusInterleukin-4MiceMice, Mutant StrainsNeuronsPresenilin-1Signal TransductionTransfectionAmyloid beta-Protein PrecursorAnti-Inflammatory AgentsInterleukin-4Presenilin-1

Identifiers

PMID20371618
PMCPMC2909296
OpenAlexW2151409678

What OpenQuestion holds

Textmetadata
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.