Evidence map›Paper›PMID 38467607›Full record

ArticleNature communications2024

Ageing impairs the regenerative capacity of regulatory T cells in mouse central nervous system remyelination.

Alerie Guzman de la Fuente, Marie Dittmer, Elise J Heesbeen, Nira de la Vega Gallardo, Jessica A White, Andrew Young, Tiree McColgan, Amy Dashwood, Katie Mayne, Sonia Cabeza-Fernández and 13 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
6.4field-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

31 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
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  7. Regulatory T cells in cancer and inflammation.Signal transduction and targeted therapy · 2026
    Review
  8. Review
  9. Engineering Immune Cell to Counteract Aging and Aging-Associated Diseases.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
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  18. EBV INFECTION OUTCOMES DETERMINED BY MONOCYTE AND TbioRxiv : the preprint server for biology · 2025
    Article
  19. Article
  20. 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

23 authors at 6 institutions in 5 countries.

Alerie Guzman de la FuenteWellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, BT9 7BL, Northern Ireland, UK. guzman_ale@isabial.es.ORCID 0000-0001-8366-4969
Marie DittmerWellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, BT9 7BL, Northern Ireland, UK.
Elise J HeesbeenWellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, BT9 7BL, Northern Ireland, UK.
Nira de la Vega GallardoWellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, BT9 7BL, Northern Ireland, UK.
Jessica A WhiteWellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, BT9 7BL, Northern Ireland, UK.ORCID 0000-0003-1081-9522
Andrew YoungWellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, BT9 7BL, Northern Ireland, UK.
Tiree McColganWellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, BT9 7BL, Northern Ireland, UK.ORCID 0009-0005-8297-2798
Amy DashwoodDepartment of Pathology, University of Cambridge, CB2 1QP, Cambridge, UK.
Katie MayneWellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, BT9 7BL, Northern Ireland, UK.
Sonia Cabeza-FernándezInstitute for Health and Biomedical Sciences of Alicante (ISABIAL), Alicante, 03010, Spain.
John FalconerWellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, BT9 7BL, Northern Ireland, UK.
Francisco Javier Rodriguez-BaenaInstituto de Neurosciencias CSIC-UMH, San Juan de Alicante, Alicante, 03550, Spain.
Christopher E McMurranDepartment of Clinical Neurosciences, University of Cambridge, Cambridge, UK.ORCID 0000-0002-8710-0930
Mohammed InayatullahInstitute of Molecular Medicine, University of Southern Denmark, 5000, Odense, Denmark.
Khalil S RawjiAltos Labs - Cambridge Institute of Science, Granta Park, Cambridge, CB21 6GP, UK.
Robin J M FranklinAltos Labs - Cambridge Institute of Science, Granta Park, Cambridge, CB21 6GP, UK.
James DooleyDepartment of Pathology, University of Cambridge, CB2 1QP, Cambridge, UK.
Adrian ListonDepartment of Pathology, University of Cambridge, CB2 1QP, Cambridge, UK.ORCID 0000-0002-6272-4085
Rebecca J IngramWellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, BT9 7BL, Northern Ireland, UK.
Vijay K TiwariWellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, BT9 7BL, Northern Ireland, UK.ORCID 0000-0003-0292-6635
Rosana PenalvaWellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, BT9 7BL, Northern Ireland, UK.
Yvonne DombrowskiWellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, BT9 7BL, Northern Ireland, UK.ORCID 0000-0003-1732-6288
Denise C FitzgeraldWellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, BT9 7BL, Northern Ireland, UK. d.fitzgerald@qub.ac.uk.ORCID 0000-0002-8608-430X
Queen's University Belfast · GBUniversity of Cambridge · GBGranta Design (United Kingdom) · GBInstituto de Neurociencias · ESBabraham Institute · GBUniversity of Southern Denmark · DK

Funding

Biotechnology and Biological Sciences Research Council BB/J01026X/1Wellcome Trust
6 · The paper itself

Abstract

Myelin regeneration (remyelination) is essential to prevent neurodegeneration in demyelinating diseases such as Multiple Sclerosis, however, its efficiency declines with age. Regulatory T cells (Treg) recently emerged as critical players in tissue regeneration, including remyelination. However, the effect of ageing on Treg-mediated regenerative processes is poorly understood. Here, we show that expansion of aged Treg does not rescue age-associated remyelination impairment due to an intrinsically diminished capacity of aged Treg to promote oligodendrocyte differentiation and myelination in male and female mice. This decline in regenerative Treg functions can be rescued by a young environment. We identified Melanoma Cell Adhesion Molecule 1 (MCAM1) and Integrin alpha 2 (ITGA2) as candidates of Treg-mediated oligodendrocyte differentiation that decrease with age. Our findings demonstrate that ageing limits the neuroregenerative capacity of Treg, likely limiting their remyelinating therapeutic potential in aged patients, and describe two mechanisms implicated in Treg-driven remyelination that may be targetable to overcome this limitation.

Indexed as

RemyelinationAgedAgingAnimalsCell DifferentiationCentral Nervous SystemFemaleHumansMaleMiceMyelin SheathOligodendrogliaT-Lymphocytes, Regulatory

Identifiers

PMID38467607
PMCPMC10928230
OpenAlexW4392647011

What Socratic 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 Socratic graph.