Evidence map›Paper›PMID 38772365›Full record

ArticleImmunity2024

Metabolic coordination between skin epithelium and type 17 immunity sustains chronic skin inflammation.

Ipsita Subudhi, Piotr Konieczny, Aleksandr Prystupa, Rochelle L Castillo, Erica Sze-Tu, Yue Xing, Daniel Rosenblum, Ilana Reznikov, Ikjot Sidhu, Cynthia Loomis and 7 more

Abstract read
In one paragraph

Article in Immunity, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing 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

61 citing papers in PubMed.

  1. Article
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  14. Nutrients · 2026
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors.

Ipsita SubudhiDepartment of Pathology, NYU Langone Health, New York, NY 10016, USA.
Piotr KoniecznyDepartment of Pathology, NYU Langone Health, New York, NY 10016, USA. Electronic address: piotr.konieczny@nyulangone.org.
Aleksandr PrystupaDepartment of Pathology, NYU Langone Health, New York, NY 10016, USA; Applied Bioinformatics Laboratories, NYU Langone Health, New York, NY 10016, USA.
Rochelle L CastilloDivision of Rheumatology, Department of Medicine, NYU Langone Health, New York, NY 10016, USA; Psoriatic Arthritis Center, NYU Langone Health, New York, NY 10016, USA.
Erica Sze-TuDepartment of Pathology, NYU Langone Health, New York, NY 10016, USA.
Yue XingDepartment of Pathology, NYU Langone Health, New York, NY 10016, USA.
Daniel RosenblumDepartment of Pathology, NYU Langone Health, New York, NY 10016, USA.
Ilana ReznikovDepartment of Pathology, NYU Langone Health, New York, NY 10016, USA.
Ikjot SidhuDepartment of Pathology, NYU Langone Health, New York, NY 10016, USA; Applied Bioinformatics Laboratories, NYU Langone Health, New York, NY 10016, USA.
Cynthia LoomisDepartment of Pathology, NYU Langone Health, New York, NY 10016, USA.
Catherine P LuThe Hansjörg Wyss Department of Plastic Surgery and Department of Cell Biology, NYU Langone Health, New York, NY 10016, USA.
Niroshana AnandasabapathyDepartment of Dermatology, Weill Cornell Medicine, New York, NY 10026, USA.
Mayte Suárez-FariñasDepartment of Genetics and Genomic Science, Department of Population Health Science and Policy, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Johann E GudjonssonDepartment of Dermatology, University of Michigan, Ann Arbor, MI 48109, USA.
Aristotelis TsirigosApplied Bioinformatics Laboratories, NYU Langone Health, New York, NY 10016, USA; Precision Medicine Institute, Department of Medicine, NYU Langone Health, New York, NY 10016, USA.
Jose U ScherDivision of Rheumatology, Department of Medicine, NYU Langone Health, New York, NY 10016, USA; NYU Colton Center for Autoimmunity, Department of Medicine, NYU Langone Health, New York, NY 10016, USA.
Shruti NaikDepartment of Pathology, NYU Langone Health, New York, NY 10016, USA; NYU Colton Center for Autoimmunity, Department of Medicine, NYU Langone Health, New York, NY 10016, USA; Ronald O. Perelman Department of Dermatology, Department of Medicine, Perlmutter Cancer Center, NYU Langone Health, New York, NY 10016, USA. Electronic address: shruti.naik@nyulangone.org.

Funding

Project-005UL1TR001445 · NCATS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BREDELLA, MIRIAM ANTOINETTE, HOCHMAN, JUDITH S · 2015 to 2025
$103.5M
ELLIPSS: ELucidating the Landscape of Immunoendotypes in Psoriatic Skin and SynoviumUC2AR081029 · NIAMS · UNIVERSITY OF ROCHESTER · PI Johann Eli Gudjonsson, Wilson Liao · 2022 to 2026
$7.9M
University of Michigan Skin Biology and Diseases Resource-based CenterP30AR075043 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Johann Eli Gudjonsson · 2019 to 2026
$6.6M
NRSA Training CoreTL1TR001447 · NCATS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI MICOLI, KEITH J. · 2015 to 2025
$5.9M
Skin Biology and Diseases Resource-based Center at Mount SinaiP30AR079200 · NIAMS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Elena Ezhkova · 2021 to 2026
$5.2M
Interrogating unique DC adaptations to tissue to promote barrier immunity and toleranceR01AR080436 · NIAMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI Niroshana Anandasabapathy · 2022 to 2026
$3.5M
Mechanisms of immune-epithelial crosstalk in tissue repairR01AI168462 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Shruti Naik · 2022 to 2026
$3.1M
Translational Basic and Clinical Research Training in RheumatologyT32AR069515 · NIAMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Jill P Buyon, Jose U. Scher · 2017 to 2026
$2.9M
Decoding microbe-epithelial stem cell interactions in health and diseaseDP2AR079173 · NIAMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI NAIK, SHRUTI · 2020 to 2020
$2.5M
Harnessing the effects of Ror gamma t cells on epidermal stem cells and commensal microbes to promote efficient wound repairK22AI135099 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI NAIK, SHRUTI · 2018 to 2019
$268k
Decoding the repair and immunomodulatory functions of lymphatic vessels in wound healingK99AR083536 · NIAMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI KONIECZNY, PIOTR · 2024 to 2025
$215k
NCATS NIH HHS TL1 TR001447NCATS NIH HHS UL1 TR001445NIAID NIH HHS K22 AI135099NIAID NIH HHS R01 AI168462NIAMS NIH HHS DP2 AR079173NIAMS NIH HHS K99 AR083536NIAMS NIH HHS P30 AR075043NIAMS NIH HHS P30 AR079200NIAMS NIH HHS R01 AR080436NIAMS NIH HHS T32 AR069515NIAMS NIH HHS UC2 AR081029
6 · The paper itself

Abstract

Inflammatory epithelial diseases are spurred by the concomitant dysregulation of immune and epithelial cells. How these two dysregulated cellular compartments simultaneously sustain their heightened metabolic demands is unclear. Single-cell and spatial transcriptomics (ST), along with immunofluorescence, revealed that hypoxia-inducible factor 1α (HIF1α), downstream of IL-17 signaling, drove psoriatic epithelial remodeling. Blocking HIF1α in human psoriatic lesions ex vivo impaired glycolysis and phenocopied anti-IL-17 therapy. In a murine model of skin inflammation, epidermal-specific loss of HIF1α or its target gene, glucose transporter 1, ameliorated epidermal, immune, vascular, and neuronal pathology. Mechanistically, glycolysis autonomously fueled epithelial pathology and enhanced lactate production, which augmented the γδ T17 cell response. RORγt-driven genetic deletion or pharmacological inhibition of either lactate-producing enzymes or lactate transporters attenuated epithelial pathology and IL-17A expression in vivo. Our findings identify a metabolic hierarchy between epithelial and immune compartments and the consequent coordination of metabolic processes that sustain inflammatory disease.

Indexed as

GlycolysisHypoxia-Inducible Factor 1, alpha SubunitInterleukin-17AnimalsChronic DiseaseDisease Models, AnimalEpitheliumGlucose Transporter Type 1HumansInflammationLactic AcidMiceMice, Inbred C57BLMice, KnockoutNuclear Receptor Subfamily 1, Group F, Member 3PsoriasisGlucose Transporter Type 1Hif1a protein, mouseHypoxia-Inducible Factor 1, alpha SubunitInterleukin-17Lactic AcidNuclear Receptor Subfamily 1, Group F, Member 3epitheliumglycolysisHIF1αinflammationlactatemetabolismskintype 17 cells

Identifiers

PMID38772365
PMCPMC11236527

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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.