Evidence map›Paper›PMID 23824053›Full record

ArticlePloS one2013

Enhanced Chemokine Receptor Expression on Leukocytes of Patients with Alzheimer's Disease.

David Goldeck, Anis Larbi, Mariavaleria Pellicanó, Iftikhar Alam, Inga Zerr, Christian Schmidt, Tamas Fulop, Graham Pawelec

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

27 citing papers in PubMed, 60 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Exploring inflammation-related protein expression and its relationship with TSPO PET in Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    Article
  6. Article
  7. T Cells Trafficking into the Brain in Aging and Alzheimer's Disease.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2024
    Review
  8. The intricate role of CCL5/CCR5 axis in Alzheimer disease.Journal of neuropathology and experimental neurology · 2023
    Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Acquired immunity and Alzheimer's disease.Journal of biomedical research · 2022
    Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. Entanglement of CCR5 and Alzheimer's Disease.Frontiers in aging neuroscience · 2019
    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

8 authors at 4 institutions in 4 countries.

David GoldeckTübingen Ageing and Tumour Immunology Group, Center for Medical Research, University of Tübingen, Tübingen, Germany.
Anis Larbi
Mariavaleria Pellicanó
Iftikhar Alam
Inga Zerr
Christian Schmidt
Tamas Fulop
Graham Pawelec
University of Tübingen · DEUniversity of Göttingen · DESingapore Immunology Network · SGUniversité de Sherbrooke · CA

Funding

CIHR 106634
6 · The paper itself

Abstract

Although primarily a neurological complaint, systemic inflammation is present in Alzheimer's Disease, with higher than normal levels of proinflammatory cytokines and chemokines in the periphery as well as the brain. A gradient of these factors may enhance recruitment of activated immune cells into the brain via chemotaxis. Here, we investigated the phenotypes of circulating immune cells in AD patients with multi-colour flow cytometry to determine whether their expression of chemokine receptors is consistent with this hypothesis. In this study, we confirmed our previously reported data on the shift of early- to late-differentiated CD4+ T-cells in AD patients. The percentage of cells expressing CD25, a marker of acute T-cell activation, was higher in patients than in age-matched controls, and percentages of CCR6+ cells were elevated. This chemokine receptor is primarily expressed on pro-inflammatory memory cells and Th17 cells. The proportion of cells expressing CCR4 (expressed on Th2 cells) and CCR5 (Th1 cells and dendritic cells) was also greater in patients, and was more pronounced on CD4+ than CD8+ T-cells. These findings allow a more detailed insight into the systemic immune status of patients with Alzheimer's disease and suggest possible novel targets for immune therapy.

Indexed as

Alzheimer DiseaseCase-Control StudiesCD4-Positive T-LymphocytesFemaleHumansImmunologic MemoryImmunophenotypingInterleukin-2 Receptor alpha SubunitLeukocytesMaleReceptors, ChemokineInterleukin-2 Receptor alpha SubunitReceptors, Chemokine

Identifiers

PMID23824053
PMCPMC3688934
OpenAlexW2093241348

What OpenQuestion holds

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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.