Evidence map›Paper›PMID 37734370›Full record

ArticleCell metabolism2023

Regulatory T cells require IL6 receptor alpha signaling to control skeletal muscle function and regeneration.

Maike Becker, Sini S Joseph, Francisco Garcia-Carrizo, Robby Z Tom, Daria Opaleva, Isabelle Serr, Matthias H Tschöp, Tim J Schulz, Susanna M Hofmann, Carolin Daniel

Open access · hybridAbstract read
In one paragraph

Article in Cell metabolism, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed, 1 pooled it
8.3field-weighted citation impact, top 2% 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

53 citing papers in PubMed, 1 synthesis or guideline pooled it, 60 citations in OpenAlex.

  1. Pooled it
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  17. Thymic regeneration and tumor immunotherapy.Frontiers in immunology · 2026
    Review
  18. IL-27 promotes Treg cell expression of CD122 and fitness at homeostasis.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  19. Article
  20. 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

10 authors at 3 institutions in 1 country.

Maike BeckerResearch Unit Type 1 Diabetes Immunology, Helmholtz Diabetes Center at Helmholtz Zentrum München, German Research Center for Environmental Health, 85764 Munich-Neuherberg, Germany; German Center for Diabetes Research (DZD), 85764 Munich-Neuherberg, Germany.
Sini S JosephGerman Center for Diabetes Research (DZD), 85764 Munich-Neuherberg, Germany; Institute for Diabetes and Obesity, Helmholtz Diabetes Center at Helmholtz Zentrum München, German Research Center for Environmental Health, 85764 Munich-Neuherberg, Germany; Division of Metabolic Diseases, Department of Medicine, Technische Universität München, 80333 Munich, Germany.
Francisco Garcia-CarrizoGerman Center for Diabetes Research (DZD), 85764 Munich-Neuherberg, Germany; Department of Adipocyte Development and Nutrition, German Institute of Human Nutrition Potsdam-Rehbrücke, 14558 Nuthetal, Germany.
Robby Z TomGerman Center for Diabetes Research (DZD), 85764 Munich-Neuherberg, Germany; Institute for Diabetes and Regeneration, Helmholtz Diabetes Center at Helmholtz Zentrum München, German Research Center for Environmental Health, 85764 Munich-Neuherberg, Germany; Department of Medicine IV, University Hospital, LMU Munich, 80336 Munich, Germany.
Daria OpalevaResearch Unit Type 1 Diabetes Immunology, Helmholtz Diabetes Center at Helmholtz Zentrum München, German Research Center for Environmental Health, 85764 Munich-Neuherberg, Germany; German Center for Diabetes Research (DZD), 85764 Munich-Neuherberg, Germany.
Isabelle SerrResearch Unit Type 1 Diabetes Immunology, Helmholtz Diabetes Center at Helmholtz Zentrum München, German Research Center for Environmental Health, 85764 Munich-Neuherberg, Germany; German Center for Diabetes Research (DZD), 85764 Munich-Neuherberg, Germany.
Matthias H TschöpGerman Center for Diabetes Research (DZD), 85764 Munich-Neuherberg, Germany; Institute for Diabetes and Obesity, Helmholtz Diabetes Center at Helmholtz Zentrum München, German Research Center for Environmental Health, 85764 Munich-Neuherberg, Germany; Division of Metabolic Diseases, Department of Medicine, Technische Universität München, 80333 Munich, Germany.
Tim J SchulzGerman Center for Diabetes Research (DZD), 85764 Munich-Neuherberg, Germany; Department of Adipocyte Development and Nutrition, German Institute of Human Nutrition Potsdam-Rehbrücke, 14558 Nuthetal, Germany; University of Potsdam, Institute of Nutritional Science, Potsdam-Rehbrücke, 14558 Nuthetal, Germany.
Susanna M HofmannGerman Center for Diabetes Research (DZD), 85764 Munich-Neuherberg, Germany; Institute for Diabetes and Regeneration, Helmholtz Diabetes Center at Helmholtz Zentrum München, German Research Center for Environmental Health, 85764 Munich-Neuherberg, Germany; Department of Medicine IV, University Hospital, LMU Munich, 80336 Munich, Germany.
Carolin DanielResearch Unit Type 1 Diabetes Immunology, Helmholtz Diabetes Center at Helmholtz Zentrum München, German Research Center for Environmental Health, 85764 Munich-Neuherberg, Germany; German Center for Diabetes Research (DZD), 85764 Munich-Neuherberg, Germany; Division of Clinical Pharmacology, Department of Medicine IV, Ludwig-Maximilians-Universität München, 80337 Munich, Germany. Electronic address: carolin.daniel@helmholtz-munich.de.
Helmholtz Zentrum München · DEDeutsches Diabetes-Zentrum e.V. · DEUniversity of Potsdam · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Muscle-residing regulatory T cells (Tregs) control local tissue integrity and function. However, the molecular interface connecting Treg-based regulation with muscle function and regeneration remains largely unexplored. Here, we show that exercise fosters a stable induction of highly functional muscle-residing Tregs with increased expression of amphiregulin (Areg), EGFR, and ST2. Mechanistically, we find that mice lacking IL6Rα on T cells (TKO) harbor significant reductions in muscle Treg functionality and satellite and fibro-adipogenic progenitor cells, which are required for muscle regeneration. Using exercise and sarcopenia models, IL6Rα TKO mice demonstrate deficits in Tregs, their functional maturation, and a more pronounced decline in muscle mass. Muscle injury models indicate that IL6Rα TKO mice have significant disabilities in muscle regeneration. Treg gain of function restores impaired muscle repair in IL6Rα TKO mice. Of note, pharmacological IL6R blockade in WT mice phenocopies deficits in muscle function identified in IL6Rα TKO mice, thereby highlighting the clinical implications of the findings.

Indexed as

Muscle, SkeletalT-Lymphocytes, RegulatoryAdipogenesisAnimalsMiceReceptors, Interleukin-6Signal TransductionReceptors, Interleukin-6exerciseIL6Ra signalingimmune-metabolic crosstalkimmune tissue crosstalkimmunometabolisminjurymuscle functionniche-specific Tregstissue Tregsvoluntary wheel running

Identifiers

PMID37734370
PMCPMC10563138
OpenAlexW4386887276

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.