Evidence map›Paper›PMID 36215678›Full record

ArticleEMBO reports2022

Lactate induces metabolic and epigenetic reprogramming of pro-inflammatory Th17 cells.

Aleksandra Lopez Krol, Hannah P Nehring, Felix F Krause, Anne Wempe, Hartmann Raifer, Andrea Nist, Thorsten Stiewe, Wilhelm Bertrams, Bernd Schmeck, Maik Luu and 5 more

Open access · greenAbstract read
In one paragraph

Article in EMBO reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 116 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
116citing papers in PubMed, 1 pooled it
11.9field-weighted citation impact, top 1% 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

116 citing papers in PubMed, 1 synthesis or guideline pooled it, 152 citations in OpenAlex.

  1. Pooled it
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  5. Review
  6. On the Edge of Benefit and Harm: Reactive Oxygen Species in Cancer.International journal of molecular sciences · 2026
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  15. Upregulation of mScience China. Life sciences · 2026
    Article
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  20. Article

56 more citing papers are in PubMed but not listed here.

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

15 authors at 4 institutions in 1 country.

Aleksandra Lopez KrolInstitute for Medical Microbiology and Hygiene, Philipps-University, Marburg, Germany.
Hannah P NehringInstitute for Medical Microbiology and Hygiene, Philipps-University, Marburg, Germany.ORCID 0000-0002-7964-2107
Felix F KrauseInstitute for Medical Microbiology and Hygiene, Philipps-University, Marburg, Germany.
Anne WempeInstitute for Medical Microbiology and Hygiene, Philipps-University, Marburg, Germany.
Hartmann RaiferFlow Cytometry Core Facility, Philipps-University, Marburg, Germany.
Andrea NistGenomics Core Facility, Philipps-University, Marburg, Germany.
Thorsten StieweGenomics Core Facility, Philipps-University, Marburg, Germany.ORCID 0000-0003-0134-7826
Wilhelm BertramsGerman Center for Lung Research (DZL), Philipps-University, Marburg, Germany.ORCID 0000-0002-2767-3606
Bernd SchmeckGerman Center for Lung Research (DZL), Philipps-University, Marburg, Germany.
Maik LuuLehrstuhl für Zelluläre Immuntherapie, Medizinische Klinik und Poliklinik II, Universitätsklinikum Würzburg, Würzburg, Germany.
Hanna LeisterInstitute for Medical Microbiology and Hygiene, Philipps-University, Marburg, Germany.
Ho-Ryun ChungInstitute for Medical Bioinformatics and Biostatistics, Philipps-University, Marburg, Germany.
Uta-Maria BauerInstitute for Medical Bioinformatics and Biostatistics, Philipps-University, Marburg, Germany.ORCID 0000-0003-1344-9117
Till AdhikaryInstitute for Medical Bioinformatics and Biostatistics, Philipps-University, Marburg, Germany.
Alexander VisekrunaInstitute for Medical Microbiology and Hygiene, Philipps-University, Marburg, Germany.ORCID 0000-0002-5207-9545
Institute of Medical Microbiology and Hygiene · DEPhilipps University of Marburg · DEGerman Center for Lung Research · DEUniversitätsklinikum Würzburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Increased lactate levels in the tissue microenvironment are a well-known feature of chronic inflammation. However, the role of lactate in regulating T cell function remains controversial. Here, we demonstrate that extracellular lactate predominantly induces deregulation of the Th17-specific gene expression program by modulating the metabolic and epigenetic status of Th17 cells. Following lactate treatment, Th17 cells significantly reduced their IL-17A production and upregulated Foxp3 expression through ROS-driven IL-2 secretion. Moreover, we observed increased levels of genome-wide histone H3K18 lactylation, a recently described marker for active chromatin in macrophages, in lactate-treated Th17 cells. In addition, we show that high lactate concentrations suppress Th17 pathogenicity during intestinal inflammation in mice. These results indicate that lactate is capable of reprogramming pro-inflammatory T cell phenotypes into regulatory T cells.

Indexed as

Lactic AcidTh17 CellsAnimalsEpigenomicsMiceLactic Acidhistone lactylationimmunometabolismlactateTh17 cellsTregs

Identifiers

PMID36215678
PMCPMC9724659
OpenAlexW4304141613

What OpenQuestion holds

Textmetadata
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.