ReviewAdvances in experimental medicine and biology2026
The Role of Short-Chain Fatty Acids Produced by Oral Bacteria in Modulating Oral Immunity.
Review in Advances in experimental medicine and biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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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.
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.
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Who cites it
1 citing paper in PubMed.
- The oral microbiota in oral squamous cell carcinoma: unravelling mechanisms and clinical potential.Cancer cell international · 2026Review
Corrections and comments
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Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Dental plaque is a complex biofilm composed of various bacterial species. These bacteria metabolize nutrients, producing high concentrations of short-chain fatty acids (SCFAs) as metabolic by-products, including acetate, propionate, butyrate, isobutyrate, isovalerate, and others. SCFAs are also produced by colonic bacteria. Given that the concentration of SCFAs is significantly higher in the colon than in dental plaque, most of the existing literature focuses on the intestinal context. Following the discovery of SCFA receptors, transporters, and their histone deacetylase (HDAC) inhibitory activities, research on the effects of SCFAs on the immune system has gained increasing attention. Additionally, certain SCFAs induce cell death in periodontal tissues, leading to the release of intracellular molecules that act as damage-associated molecular patterns (DAMPs), thereby influencing the immune system. In this chapter, we first describe oral bacteria that produce SCFAs and compare the concentrations of these SCFAs in the oral cavity with those in the intestinal tract. Then, we provide an overview of the SCFA receptors, the transporters required for their transmembrane passage, and the histone deacetylase inhibitory effects of certain SCFAs. We then discuss how these mechanisms contribute to, or are hypothesized to influence, the effects of SCFAs on various immune cells. After reviewing various forms of cell death capable of triggering DAMP release, we will discuss the potential role of SCFA-induced gingival epithelial cell death in promoting the release of DAMPs and its contribution to gingival inflammation.
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Registered trials
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.