# Oral ginger-derived extracellular vesicles ameliorate arthritis via anti-inflammatory actions of microRNA-149 and 6-gingerol

**Authors:** Hiroki Kaneta, Tomoyuki Nakasa, Dilimulati Yimiti, Dan Moriwaki, Riku Kawasaki, Toshihiko Ogura, Shigeru Miyaki, Nobuo Adachi

PMC · DOI: 10.1016/j.omtn.2026.102840 · Molecular Therapy. Nucleic Acids · 2026-01-19

## TL;DR

Ginger-derived extracellular vesicles reduce arthritis inflammation and joint damage when taken orally, offering a natural, non-invasive treatment option.

## Contribution

The study introduces ginger-derived extracellular vesicles as a novel oral therapy for rheumatoid arthritis.

## Key findings

- GDEVs suppressed pro-inflammatory cytokines and inhibited RA synovial fibroblast proliferation and migration.
- Oral GDEVs reduced arthritis severity, synovitis, and osteoclast activation in a mouse model.
- miR-149 in GDEVs was identified as a key regulator of anti-inflammatory pathways.

## Abstract

Ginger-derived extracellular vesicles (GDEVs) have emerged as a novel anti-inflammatory agent with advantages such as oral bioavailability, natural origin, and cost-effective large-scale production. This study evaluated the therapeutic potential of GDEVs in rheumatoid arthritis (RA), a chronic autoimmune disease characterized by synovial inflammation and joint destruction. We conducted both in vitro and in vivo experiments using synovial fibroblasts derived from RA patients and a collagen antibody-induced arthritis (CAIA) mouse model. In vitro, GDEVs significantly suppressed the expression of pro-inflammatory cytokines tumor necrosis factor-α (TNF-α) and interleukin (IL)-1β and downstream mediators IL-6, Cox-2, and matrix metalloproteinase 3 (MMP3) and inhibited the proliferation and migration of RA synovial fibroblasts. In vivo, oral administration of GDEVs to CAIA mice reduced arthritis severity, attenuated synovitis, preserved cartilage integrity, and suppressed osteoclast activation. GDEVs were stable against gastric digestion and were efficiently taken up by intestinal cells, supporting their oral availability. Microarray and RNA sequencing identified miR-149 as a key regulatory molecule in GDEVs, associated with the suppression of inflammation-related signaling pathways, including Ras signaling and mitogen-activated protein kinase (MAPK) cascades. These findings highlight the potential of GDEVs as an anti-inflammatory therapy for RA. Given their stability and bioavailability, the oral administration of GDEVs could be a promising non-invasive treatment for future clinical applications.

Nakasa and colleagues show that orally administered ginger-derived extracellular vesicles (GDEVs), enriched with miR-149 and 6-gingerol, alleviate rheumatoid arthritis by modulating inflammatory pathways. Their study highlights a novel, plant-based, non-invasive therapeutic strategy leveraging the bioactive and immunomodulatory properties of GDEVs with potential for clinical translation.

## Linked entities

- **Genes:** MIR149 (microRNA 149) [NCBI Gene 406941]
- **Proteins:** TNF (tumor necrosis factor), IL1B (interleukin 1 beta), IL6 (interleukin 6), COX2 (cytochrome c oxidase subunit II), MMP3 (matrix metallopeptidase 3)
- **Chemicals:** 6-gingerol (PubChem CID 3473)
- **Diseases:** rheumatoid arthritis (MONDO:0008383)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Diseases:** CAIA (MESH:D001169), inflammation (MESH:D007249), arthritis (MESH:D001168), synovitis (MESH:D013585), RA (MESH:D001172), joint destruction (MESH:D008105), autoimmune disease (MESH:D001327)
- **Chemicals:** 6-gingerol (MESH:C007845)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12887272/full.md

## References

84 references — full list in the complete paper: https://tomesphere.com/paper/PMC12887272/full.md

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Source: https://tomesphere.com/paper/PMC12887272