Evidence map›Paper›PMID 35380608›Full record

ArticleThe Journal of experimental medicine2022

IL-17A-producing γδT cells promote muscle regeneration in a microbiota-dependent manner.

Alexander O Mann, Bola S Hanna, Andrés R Muñoz-Rojas, Inga Sandrock, Immo Prinz, Christophe Benoist, Diane Mathis

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

29 citing papers in PubMed, 38 citations in OpenAlex.

  1. A who's who of cell types in skeletal muscle.Communications biology · 2026
    Review
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  13. Murine gut microbiota dysbiosis via enteric infection modulates the foreign body response to a distal biomaterial implant.Proceedings of the National Academy of Sciences of the United States of America · 2025
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  20. γδ T cell antigen receptor polyspecificity enables T cell responses to a broad range of immune challenges.Proceedings of the National Academy of Sciences of the United States of America · 2024
    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

7 authors at 3 institutions in 2 countries.

Alexander O Mann *Department of Immunology, Harvard Medical School, Boston, MA.ORCID 0000-0002-5927-1396
Bola S Hanna *Department of Immunology, Harvard Medical School, Boston, MA.ORCID 0000-0002-9074-8375
Andrés R Muñoz-RojasDepartment of Immunology, Harvard Medical School, Boston, MA.ORCID 0000-0002-1251-723X
Inga SandrockInstitute of Immunology, Hannover Medical School, Hannover, Germany.ORCID 0000-0002-7607-8571
Immo PrinzInstitute of Immunology, Hannover Medical School, Hannover, Germany.ORCID 0000-0002-8789-9578
Christophe BenoistDepartment of Immunology, Harvard Medical School, Boston, MA.ORCID 0000-0003-1172-6555
Diane MathisDepartment of Immunology, Harvard Medical School, Boston, MA.ORCID 0000-0002-6110-4626
Brigham and Women's Hospital · USMedizinische Hochschule Hannover · DEUniversität Hamburg · DE

Funding

Muscle Tregs in health and diseaseR01AR070334 · NIAMS · HARVARD MEDICAL SCHOOL · PI MATHIS, DIANE J · 2016 to 2025
$3.7M
Deutsche Forschungsgemeinschaft HA 8510/1JPB FoundationNIAMS NIH HHS R01 AR070334
6 · The paper itself

Abstract

Subsequent to acute injury, skeletal muscle undergoes a stereotypic regenerative process that reestablishes homeostasis. Various types of innate and adaptive immunocytes exert positive or negative influences at specific stages along the course of muscle regeneration. We describe an unanticipated role for γδT cells in promoting healthy tissue recovery after injection of cardiotoxin into murine hindlimb muscle. Within a few days of injury, IL-17A-producing γδT cells displaying primarily Vγ6+ antigen receptors accumulated at the wound site. Punctual ablation experiments showed that these cells boosted early inflammatory events, notably recruitment of neutrophils; fostered the proliferation of muscle stem and progenitor cells; and thereby promoted tissue regeneration. Supplementation of mice harboring low numbers of IL-17A+ γδT cells with recombinant IL-17A largely reversed their inflammatory and reparative defects. Unexpectedly, the accumulation and influences of γδT cells in this experimental context were microbiota dependent, unveiling an orthogonal perspective on the treatment of skeletal muscle pathologies such as catastrophic wounds, wasting, muscular dystrophies, and myositides.

Indexed as

Interleukin-17MicrobiotaMuscle DevelopmentRegenerationT-LymphocytesAnimalsMiceMice, Inbred C57BLMusclesReceptors, Antigen, T-Cell, gamma-deltaInterleukin-17Receptors, Antigen, T-Cell, gamma-delta

Identifiers

PMID35380608
PMCPMC8989184
OpenAlexW4224117093

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.