Evidence map›Paper›PMID 39741755›Full record

ArticleJournal of inflammation research2024

Influence of TNF-α Inhibitors on Gut Microbiota and Immune Modulation in Treating Ankylosing Spondylitis: Insights into Therapeutic Mechanisms and Clinical Implications.

Yue-Xing Yuan, Shou-Rui Feng, Ai-Yu Wu, Wei-Hao Wu, Pan Tian, Ai-Zhen Chen, Xiao-Mei Ma, Ling-Ling Huang, Lian Yu

Abstract read
In one paragraph

Article in Journal of inflammation research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
–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

6 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
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.

Yue-Xing Yuan *Department of Hematology and Rheumatology, Longyan First Hospital Affiliated to Fujian Medical University, Longyan, 364000, People's Republic of China.
Shou-Rui Feng *State Key Laboratory of Biocontrol, School of Life Sciences, Sun Yat-Sen University, Guangzhou, 510275, People's Republic of China.
Ai-Yu WuDepartment of Hematology and Rheumatology, Longyan First Hospital Affiliated to Fujian Medical University, Longyan, 364000, People's Republic of China.
Wei-Hao WuDepartment of Hematology and Rheumatology, Longyan First Hospital Affiliated to Fujian Medical University, Longyan, 364000, People's Republic of China.
Pan TianDepartment of Hematology and Rheumatology, Longyan First Hospital Affiliated to Fujian Medical University, Longyan, 364000, People's Republic of China.
Ai-Zhen ChenDepartment of Hematology and Rheumatology, Longyan First Hospital Affiliated to Fujian Medical University, Longyan, 364000, People's Republic of China.
Xiao-Mei MaDepartment of Hematology and Rheumatology, Longyan First Hospital Affiliated to Fujian Medical University, Longyan, 364000, People's Republic of China.
Ling-Ling HuangDepartment of Hematology and Rheumatology, Longyan First Hospital Affiliated to Fujian Medical University, Longyan, 364000, People's Republic of China.
Lian YuDepartment of Hematology and Rheumatology, Longyan First Hospital Affiliated to Fujian Medical University, Longyan, 364000, People's Republic of China.ORCID 0000-0002-8808-8048

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: This study aims to evaluate the impact of tumor necrosis factor (TNF) inhibitors on the gut microbiota in patients with ankylosing spondylitis (AS) and investigate the potential therapeutic benefits of microbial modulation. Given the role of gut microbiota in immune regulation and its association with autoimmune conditions like AS, this research seeks to identify microbial targets that could enhance treatment outcomes. Methods: Patients with AS undergoing TNF inhibitor therapy and healthy controls were recruited for this study. Gut microbiota samples were collected and analyzed using 16S rRNA gene sequencing. Assessed key parameters included α-diversity and the relative abundance of dominant phyla, such as Firmicutes, Proteobacteria, Bacteroidota, Actinobacteriota, and Fusobacteriota. Results: Tumor necrosis factor (TNF) inhibitor therapy was found to enhance the α-diversity of the gut microbiota in patients with AS. The dominant phyla identified included Firmicutes, Proteobacteria, Bacteroidota, Actinobacteriota, and Fusobacteriota. Comparative analysis showed that patients with AS had elevated levels of Proteobacteria and Pasteurellaceae, which were normalized following TNF inhibitor treatment. Functional predictive analysis suggested that pathways associated with Terpenoid backbone biosynthesis and photosynthesis were reduced in patients with AS, bringing them closer to the profiles observed in healthy controls. Conclusion: TNF inhibitors may contribute to the treatment of AS by promoting beneficial microbes, reducing the prevalence of disease-associated microbes, and modulating microbial functions. These findings bring valuable insights into the mechanisms of how TNF inhibitors act and highlight potential microbial targets for therapeutic interventions in AS.

Indexed as

ankylosing spondylitisgut microbiotaimmune system dysregulationinflammationmicrobial diversityTNF inhibitors

Identifiers

PMID39741755
PMCPMC11687288

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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.