Evidence map›Paper›PMID 39251592›Full record

ArticleNature communications2024

Local administration of regulatory T cells promotes tissue healing.

Bhavana Nayer, Jean L Tan, Yasmin K Alshoubaki, Yen-Zhen Lu, Julien M D Legrand, Sinnee Lau, Nan Hu, Anthony J Park, Xiao-Nong Wang, Daniela Amann-Zalcenstein and 7 more

Abstract 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 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing 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

60 citing papers in PubMed.

  1. Review
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  19. Review
  20. CD4iScience · 2026
    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

17 authors.

Bhavana NayerEuropean Molecular Biology Laboratory Australia, Australian Regenerative Medicine Institute, Monash University, Melbourne, VIC, Australia.ORCID 0000-0003-4234-8630
Jean L TanEuropean Molecular Biology Laboratory Australia, Australian Regenerative Medicine Institute, Monash University, Melbourne, VIC, Australia.
Yasmin K AlshoubakiEuropean Molecular Biology Laboratory Australia, Australian Regenerative Medicine Institute, Monash University, Melbourne, VIC, Australia.ORCID 0000-0001-6031-531X
Yen-Zhen LuEuropean Molecular Biology Laboratory Australia, Australian Regenerative Medicine Institute, Monash University, Melbourne, VIC, Australia.ORCID 0000-0003-4262-3436
Julien M D LegrandEuropean Molecular Biology Laboratory Australia, Australian Regenerative Medicine Institute, Monash University, Melbourne, VIC, Australia.ORCID 0000-0001-5577-5645
Sinnee LauEuropean Molecular Biology Laboratory Australia, Australian Regenerative Medicine Institute, Monash University, Melbourne, VIC, Australia.ORCID 0009-0009-7235-5680
Nan HuEuropean Molecular Biology Laboratory Australia, Australian Regenerative Medicine Institute, Monash University, Melbourne, VIC, Australia.
Anthony J ParkEuropean Molecular Biology Laboratory Australia, Australian Regenerative Medicine Institute, Monash University, Melbourne, VIC, Australia.
Xiao-Nong WangTranslational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.
Daniela Amann-ZalcensteinAdvanced Genomics Facility, Advanced Technology and Biology Division, The Walter and Eliza Hall Institute of Medical Research, Parkville, VIC, Australia.ORCID 0000-0003-4928-1846
Peter F HickeyAdvanced Genomics Facility, Advanced Technology and Biology Division, The Walter and Eliza Hall Institute of Medical Research, Parkville, VIC, Australia.ORCID 0000-0002-8153-6258
Trevor WilsonMHTP Medical Genomics Facility, Monash Health Translation Precinct, Clayton, VIC, Australia.
Gisela A KuhnInstitute for Biomechanics, ETH Zurich, Zurich, Switzerland.
Ralph MüllerInstitute for Biomechanics, ETH Zurich, Zurich, Switzerland.ORCID 0000-0002-5811-7725
Ajithkumar VasanthakumarOlivia Newton-John Cancer Research Institute, Heidelberg, VIC, Australia.ORCID 0000-0002-1620-7781
Shizuo AkiraLaboratory of Host Defense, World Premier Institute Immunology Frontier Research Center, Osaka University, Osaka, Japan.
Mikaël M MartinoEuropean Molecular Biology Laboratory Australia, Australian Regenerative Medicine Institute, Monash University, Melbourne, VIC, Australia. mikael.martino@monash.edu.ORCID 0000-0002-5012-4605

Funding

Department of Health | National Health and Medical Research Council (NHMRC) APP1140229Department of Health | National Health and Medical Research Council (NHMRC) APP1176213
6 · The paper itself

Abstract

Regulatory T cells (Tregs) are crucial immune cells for tissue repair and regeneration. However, their potential as a cell-based regenerative therapy is not yet fully understood. Here, we show that local delivery of exogenous Tregs into injured mouse bone, muscle, and skin greatly enhances tissue healing. Mechanistically, exogenous Tregs rapidly adopt an injury-specific phenotype in response to the damaged tissue microenvironment, upregulating genes involved in immunomodulation and tissue healing. We demonstrate that exogenous Tregs exert their regenerative effect by directly and indirectly modulating monocytes/macrophages (Mo/MΦ) in injured tissues, promoting their switch to an anti-inflammatory and pro-healing state via factors such as interleukin (IL)-10. Validating the key role of IL-10 in exogenous Treg-mediated repair and regeneration, the pro-healing capacity of these cells is lost when Il10 is knocked out. Additionally, exogenous Tregs reduce neutrophil and cytotoxic T cell accumulation and IFN-γ production in damaged tissues, further dampening the pro-inflammatory Mo/MΦ phenotype. Highlighting the potential of this approach, we demonstrate that allogeneic and human Tregs also promote tissue healing. Together, this study establishes exogenous Tregs as a possible universal cell-based therapy for regenerative medicine and provides key mechanistic insights that could be harnessed to develop immune cell-based therapies to enhance tissue healing.

Indexed as

Interleukin-10MacrophagesMice, Inbred C57BLT-Lymphocytes, RegulatoryWound HealingAnimalsFemaleHumansInterferon-gammaMaleMiceMonocytesSkinInterferon-gammaInterleukin-10

Identifiers

PMID39251592
PMCPMC11383969

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.