Evidence map›Paper›PMID 40615087›Full record

ArticleThe Journal of nutrition2025

Protective Role of Dietary Short-Chain Fatty Acid Propionate against Autoimmune Responses and Pathology of Systemic Lupus Erythematosus in MRL-lpr Mice.

Hui Wang, Yuejin Liang, Paul J Boor, Kamil Khanipov, Yuanyi Zhang, Xiaoying Yu, Chandra Shekar R Ambati, Nagireddy Putluri, M Firoze Khan

Abstract read
In one paragraph

Article in The Journal of nutrition, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Review
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

9 authors.

Hui WangDepartment of Pathology, University of Texas Medical Branch, Galveston, TX, United States.
Yuejin LiangDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX, United States.
Paul J BoorDepartment of Pathology, University of Texas Medical Branch, Galveston, TX, United States.
Kamil KhanipovDepartment of Pharmacology, University of Texas Medical Branch, Galveston, TX, United States.
Yuanyi ZhangDepartment of Biostatistics and Data Science, University of Texas Medical Branch, Galveston, TX, United States.
Xiaoying YuDepartment of Biostatistics and Data Science, University of Texas Medical Branch, Galveston, TX, United States.
Chandra Shekar R AmbatiAdvanced Technology Core, Baylor College of Medicine, Houston, TX, United States.
Nagireddy PutluriAdvanced Technology Core, Baylor College of Medicine, Houston, TX, United States; Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX, United States.
M Firoze KhanDepartment of Pathology, University of Texas Medical Branch, Galveston, TX, United States. Electronic address: mfkhan@utmb.edu.

Funding

Unraveling the contribution of gut microbiome in trichloroethene-mediated autoimmunityR56ES035376 · NIEHS · UNIVERSITY OF TEXAS MED BR GALVESTON · PI KHAN, M. FIROZE · 2023 to 2023
$158k
NIEHS NIH HHS R56 ES035376
6 · The paper itself

Abstract

backgroundSystemic lupus erythematosus (SLE) is a chronic autoimmune disease that affects multiple organs, including the skin and kidneys. The etiology of SLE remains unclear but involves hormonal, environmental, and genetic factors. Environmental factors, such as diet and microbiota-derived metabolites, among which short-chain fatty acids (SCFAs) are major players, can influence autoimmune disease pathogenesis.

objectivesThis study investigates the involvement of SCFAs in the pathogenesis of SLE and further investigates the effect of propionate (PA) supplementation on SLE disease outcome in MRL-lpr mice.

methodsCecal SCFAs from mouse models with varying degrees of SLE disease activities (C57BL/6, MRL+/+, and MRL-lpr) were determined by liquid chromatography/MS analysis. Five-week-old MRL-lpr mice were supplemented with PA (200 mM, via drinking water) for 6 wk, and assessed for autoimmunity and disease markers.

resultsLiquid chromatography/mass analysis of cecal SCFAs showed a significant decrease of PA in MRL-lpr mice (P < 0.001). PA treatment ameliorated the autoimmune response, evident from reduced serum autoantibodies (P < 0.05 for both antinuclear antibodies and anti-double-stranded deoxyribonucleic acid) and a significant alleviation of glomerulonephritis (P < 0.05). Furthermore, it restored the imbalances in gut microbiome composition and SCFAs, especially PA (P < 0.01). Additionally, PA treatment resulted in decreased splenic activated CD4 T cells (P < 0.05) and alterations in renal inflammatory signaling pathways.

conclusionsOur findings support the beneficial effects of PA in alleviating SLE and the therapeutic potential of PA or PA-producing bacteria for SLE.

Indexed as

autoimmune diseasemicrobiomepropionateSCFASLE

Identifiers

PMID40615087
PMCPMC12797317

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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.