Evidence map›Paper›PMID 36217178›Full record

ArticleJournal of neuroinflammation2022

Promoted CD4

Xiaolei Wu, Qi Shen, Haocai Chang, Junyu Li, Da Xing

Open access · goldAbstract read
In one paragraph

Article in Journal of neuroinflammation, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 7% 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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 45 citations in OpenAlex.

  1. Pooled it
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  3. Review
  4. Article
  5. Review
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  8. Article
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  13. Article
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  15. Article
  16. Co-transplantation of autologous treg cells: A groundbreaking cell therapy for brain diseases.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2024
    Review
  17. Review
  18. Article
  19. Review
  20. Role of the Insulin-like Growth Factor System in Neurodegenerative Disease.International journal of molecular sciences · 2024
    Review
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

5 authors at 1 institution in 1 country.

Xiaolei Wu *MOE Key Laboratory of Laser Life Science and Institute of Laser Life Science, College of Biophotonics, South China Normal University, Guangzhou, 510631, China.
Qi Shen *MOE Key Laboratory of Laser Life Science and Institute of Laser Life Science, College of Biophotonics, South China Normal University, Guangzhou, 510631, China. shenqi@scnu.edu.cn.
Haocai ChangMOE Key Laboratory of Laser Life Science and Institute of Laser Life Science, College of Biophotonics, South China Normal University, Guangzhou, 510631, China.
Junyu LiMOE Key Laboratory of Laser Life Science and Institute of Laser Life Science, College of Biophotonics, South China Normal University, Guangzhou, 510631, China.
Da XingMOE Key Laboratory of Laser Life Science and Institute of Laser Life Science, College of Biophotonics, South China Normal University, Guangzhou, 510631, China. xingda@scnu.edu.cn.
South China Normal University · CN

Funding

China Postdoctoral Science Foundation 2021M691093National Natural Science Foundation of China 61361160414; 31470072Natural Science Foundation of Guangdong Province 2014A030313419Science and Technology Plan Project of Guangzhou, China 202201010291
6 · The paper itself

Abstract

backgroundThe immune system has been implicated in synaptic plasticity, inflammation, and the progression of Alzheimer's disease (AD). However, there were few studies on improving the niche microenvironment of neural stem cells (NSCs) in the brain of AD to promote adult hippocampal neurogenesis (AHN) by regulating the function of non-parenchymal immune cells.

methodsThe lymph nodes of amyloid precursor protein/presenilin 1 (APP/PS1) and 3xTg (APP/PS1/tau) mouse models of AD were treated with photobiomodulation therapy (PBMT) for 10 J/cm

resultsOur results showed that PBMT treatment could promote AHN and reverse cognitive deficits in AD mouse model. The expression of interferon-γ (IFN-γ) and interleukin-10 (IL-10) was upregulated in the brain of these two AD models after PBMT treated, which was induced by the activation of Janus kinase 2 (JAK2)-mediated signal transducer and activator of transcription 4 (STAT4)/STAT5 signaling pathway in CD4

conclusionOur research suggests that PBMT exerts a beneficial neurogenesis modulatory effect through activating the JAK2/STAT4/STAT5 signaling pathway to promote the expression of IFN-γ/IL-10 in non-parenchymal CD4

Indexed as

Alzheimer DiseaseLow-Level Light TherapyAmyloid beta-Protein PrecursorAnimalsBrain-Derived Neurotrophic FactorCD4-Positive T-LymphocytesCognitionCulture Media, ConditionedDisease Models, AnimalDisks Large Homolog 4 ProteinInsulin-Like Growth Factor IInterferon-gammaInterleukin-10Janus Kinase 2MiceMice, TransgenicAmyloid beta-Protein PrecursorBrain-Derived Neurotrophic FactorCulture Media, ConditionedDisks Large Homolog 4 ProteinInsulin-Like Growth Factor IInterferon-gammaInterleukin-10Janus Kinase 2Presenilin-1Reactive Oxygen SpeciesSTAT4 Transcription FactorSTAT5 Transcription FactorTransforming Growth Factor beta1TubulinAlzheimer's diseaseCD4+ T cellCognitive deficitsIFN-γ/IL-10JAK2/STAT4/STAT5 pathwayNeurogenesisNSCs

Identifiers

PMID36217178
PMCPMC9549637
OpenAlexW4304112877

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.