Evidence map›Paper›PMID 39844773›Full record

ArticleCNS neuroscience & therapeutics2025

CD4-Derived Double-Negative T Cells Ameliorate Alzheimer's Disease-Like Phenotypes in the 5×FAD Mouse Model.

Yuanzi Xie, Jing Liu, Zongren Hou, Huan Wang, Kailun Liu, Xiaowei Chen, Zhen Fan, Da Li, Can Li, Yuhualei Pan and 3 more

Abstract read
In one paragraph

Article in CNS neuroscience & therapeutics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
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

13 authors.

Yuanzi XieState Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.
Jing LiuState Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.
Zongren HouUniversity of Chinese Academy of Sciences, Beijing, China.
Huan WangBeijing Clinical Research Institute, Beijing Friendship Hospital, Capital Medical University, Beijing, China.
Kailun LiuState Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.
Xiaowei ChenInstitute of Biophysics, Chinese Academy of Sciences, Beijing, China.
Zhen FanInstitute of Biophysics, Chinese Academy of Sciences, Beijing, China.
Da LiState Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.
Can LiState Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.
Yuhualei PanBeijing Clinical Research Institute, Beijing Friendship Hospital, Capital Medical University, Beijing, China.
Yushang ZhaoBeijing Clinical Research Institute, Beijing Friendship Hospital, Capital Medical University, Beijing, China.
Yanbing ZhuBeijing Clinical Research Institute, Beijing Friendship Hospital, Capital Medical University, Beijing, China.
Baoyang HuState Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.ORCID 0009-0003-8756-430X

Funding

Basic Frontier Science Research Program of CAS ZDBS-LY-SM024National Key Research and Development Program of China 2021YFA1101400Strategic Priority Research Program of CAS XDA 046205
6 · The paper itself

Abstract

backgroundAlzheimer's disease (AD) is a debilitating neurodegenerative disorder that is difficult to predict and is typically diagnosed only after symptoms manifest. Recently, CD4

objectiveThis study's aims were three-fold, to (1) evaluate the efficacy of CD4

methodsWe performed tail vein injection of transformed and amplified CD4

resultsThrough qualitative analysis, we identified 6 main themes. DNT from young wild-type mice enhance the capability of spatial learning and memory in AD mice. DNT cell treatment rejuvenates the microglial function. DNT cell treatment improves the state of oligodendrocytes. DNT cell treatment finetunes the activation of the immune system. DNT cell treatment improves the synaptic plasticity and increases the complexity of neurons. DNT cell treatment reduces the density of amyloid Beta plaques deposition in the cortex and hippocampus of 5 × FAD mice. DISCUSSION: The findings from this study reveal that DNT treatment improved spatial memory and learning abilities, reduced Aβ deposition, and enhanced synaptic plasticity, contrasting with previous reports on thymus-derived DNT cells. Additionally, CD4

Indexed as

Alzheimer DiseaseCD4-Positive T-LymphocytesAgingAmyloid beta-PeptidesAnimalsCell TransplantationDisease Models, AnimalFemaleMaleMemoryMiceMice, Inbred C57BLMicrogliaNeuronal PlasticityOligodendrogliaSpace PerceptionAmyloid beta-PeptidesAlzheimer's diseaseAβ plaquesCD4+ T cell‐derived double‐negative T cellscell therapyTCRαβ+NK1.1−CD4−CD8−

Identifiers

PMID39844773
PMCPMC11754964

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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.