Evidence map›Paper›PMID 41741465›Full record

ArticleNature communications2026

Context-specific regulatory genetic variation in MTOR dampens neutrophil-T cell crosstalk in pneumonia-associated sepsis.

Ping Zhang, Patrick MacLean, Alicia Jia, Callum R O'Neill, Alice Allcock, Ethan Prince, Bora Ozcan, Roman M Doll, Imogen Dyne, Kiki Cano-Gamez and 10 more

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

20 authors.

Ping ZhangChinese Academy of Medical Sciences Oxford Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK. ping.zhang@well.ox.ac.uk.ORCID http://orcid.org/0000-0001-7063-7769
Patrick MacLeanCentre for Human Genetics, Nuffield Department of Medicine, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0001-5702-9929
Alicia JiaCentre for Human Genetics, Nuffield Department of Medicine, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0002-0619-7313
Callum R O'NeillCentre for Human Genetics, Nuffield Department of Medicine, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0003-1903-6348
Alice AllcockCentre for Human Genetics, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Ethan PrinceCentre for Human Genetics, Nuffield Department of Medicine, University of Oxford, Oxford, UK.ORCID http://orcid.org/0009-0009-8928-1622
Bora OzcanMRC Molecular Haematology Unit, MRC Weatherall Institute of Molecular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.ORCID http://orcid.org/0009-0002-3675-3920
Roman M DollMRC Molecular Haematology Unit, MRC Weatherall Institute of Molecular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0003-3991-6043
Imogen DyneCentre for Human Genetics, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Kiki Cano-GamezCentre for Human Genetics, Nuffield Department of Medicine, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0003-2753-1226
Hanyu QinChinese Academy of Medical Sciences Oxford Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Chloe WainwrightCentre for Human Genetics, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Giuseppe ScozzafavaCentre for Human Genetics, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Andrew C BrownCentre for Human Genetics, Nuffield Department of Medicine, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0002-4951-3056
James O J DaviesMRC Molecular Haematology Unit, MRC Weatherall Institute of Molecular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0002-4108-4357
Amanda Y ChongCentre for Human Genetics, Nuffield Department of Medicine, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0003-4919-2632
Alexander J MentzerChinese Academy of Medical Sciences Oxford Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0002-4502-2209
Katie L BurnhamWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.ORCID http://orcid.org/0000-0001-8680-2933
Emma E DavenportWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.
Julian C KnightChinese Academy of Medical Sciences Oxford Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK. julian.knight@well.ox.ac.uk.ORCID http://orcid.org/0000-0002-0377-5536

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sepsis is a heterogeneous clinical syndrome with a high mortality, requiring personalised stratification strategies. Here, we characterise genetic variation that modulates MTOR, a critical regulator of metabolism and immune responses in sepsis. The effects are context specific, involving a regulatory element that affects MTOR expression in activated T cells with opposite effect in neutrophils. We show that the G-allele of the lead variant, rs4845987, which is associated with decreased risk of type 2 diabetes, reduces MTOR expression in T cells and improves survival in sepsis due to pneumonia, with effects specific to sepsis endotype. Using ex vivo models, we demonstrate that activated T cells promote immunosuppressive neutrophils through released cytokines, a process dampened by hypoxia and the mTOR inhibitor rapamycin. Our work demonstrates an epigenetic mechanism fine-tuning MTOR transcription and T cell activity via the variant-containing regulatory element, which further exhibits an allelic effect upon vitamin C treatment. These findings reveal how genetic variation interacts with disease state to modulate immune cell-cell communication, providing a framework for stratified therapy in sepsis.

Indexed as

NeutrophilsPneumoniaSepsisT-LymphocytesTOR Serine-Threonine KinasesAllelesAnimalsAscorbic AcidCell CommunicationCytokinesDiabetes Mellitus, Type 2FemaleGenetic VariationHumansMalePolymorphism, Single NucleotideAscorbic AcidCytokinesMTOR protein, humanTOR Serine-Threonine Kinases

Identifiers

PMID41741465
PMCPMC13057173

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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.