Evidence map›Paper›PMID 37416482›Full record

ArticleiScience2023

Pharmacologic inhibition of glycolysis prevents the development of lupus by altering the gut microbiome in mice.

Ahmed S Elshikha, Yong Ge, Josephine Brown, Nathalie Kanda, Mojgan Zadeh, Georges Abboud, Seung-Chul Choi, Gregg Silverman, Timothy J Garrett, William L Clapp and 2 more

Open access · goldAbstract read
In one paragraph

Article in iScience, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

11 citing papers in PubMed, 12 citations in OpenAlex.

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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

12 authors at 3 institutions in 1 country.

Ahmed S ElshikhaDepartment of Pathology, Immunology, and Laboratory Medicine, University of Florida, Gainesville, FL 32610, USA.
Yong GeDepartment of Microbiology, Immunology, and Molecular Genetics, University of Texas Health, San Antonio, TX 78229, USA.
Josephine BrownDepartment of Pathology, Immunology, and Laboratory Medicine, University of Florida, Gainesville, FL 32610, USA.
Nathalie KandaDepartment of Microbiology, Immunology, and Molecular Genetics, University of Texas Health, San Antonio, TX 78229, USA.
Mojgan ZadehDepartment of Microbiology, Immunology, and Molecular Genetics, University of Texas Health, San Antonio, TX 78229, USA.
Georges AbboudDepartment of Pathology, Immunology, and Laboratory Medicine, University of Florida, Gainesville, FL 32610, USA.
Seung-Chul ChoiDepartment of Microbiology, Immunology, and Molecular Genetics, University of Texas Health, San Antonio, TX 78229, USA.
Gregg SilvermanThe Laboratory of B Cell Immunobiology and the Division of Rheumatology, NYU School of Medicine, New York, NY 10016, USA.
Timothy J GarrettDepartment of Pathology, Immunology, and Laboratory Medicine, University of Florida, Gainesville, FL 32610, USA.
William L ClappDepartment of Pathology, Immunology, and Laboratory Medicine, University of Florida, Gainesville, FL 32610, USA.
Mansour MohamadzadehDepartment of Microbiology, Immunology, and Molecular Genetics, University of Texas Health, San Antonio, TX 78229, USA.
Laurence MorelDepartment of Microbiology, Immunology, and Molecular Genetics, University of Texas Health, San Antonio, TX 78229, USA.
The University of Texas Health Science Center at San Antonio · USUniversity of Florida · USNew York University · US

Funding

Determinants of follicular helper T cell expansion in lupusR01AI154630 · NIAID · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI MOREL, LAURENCE, ZADEH, MANSOUR M · 2020 to 2025
$6.3M
Bacterial surface layer-specific immune protection against gut microbial infectionR01DK109560 · NIDDK · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI ZADEH, MANSOUR M · 2016 to 2024
$3.5M
Gut dysbiosis and tryptophan metabolism in lupusR01AI143313 · NIAID · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Laurence Morel, Gregg Joshua Silverman · 2019 to 2026
$3.3M
NIAID NIH HHS R01 AI143313NIAID NIH HHS R01 AI154630NIDDK NIH HHS R01 DK109560
6 · The paper itself

Abstract

Gut dysbiosis has been associated with lupus pathogenesis, and fecal microbiota transfers (FMT) from lupus-prone mice shown to induce autoimmune activation into healthy mice. The immune cells of lupus patients exhibit an increased glucose metabolism and treatments with 2-deoxy-D-glucose (2DG), a glycolysis inhibitor, are therapeutic in lupus-prone mice. Here, we showed in two models of lupus with different etiologies that 2DG altered the composition of the fecal microbiome and associated metabolites. In both models, FMT from 2DG-treated mice protected lupus-prone mice of the same strain from the development of glomerulonephritis, reduced autoantibody production as well as the activation of CD4

Indexed as

Immune system disorderMicrobiomePharmaceutical science

Identifiers

PMID37416482
PMCPMC10320500
OpenAlexW4380988570

What Socratic 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 Socratic graph.