ReviewJournal of nanobiotechnology2026
Plant-derived extracellular vesicles as tools and targets for inflammatory diseases.
Review in Journal of nanobiotechnology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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.
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.
Who cites it
2 citing papers in PubMed.
- Plant-derived extracellular vesicles as bioactive nanoplatforms: Biogenesis, therapeutic evidence, and translational challenges.Biochemistry and biophysics reports · 2026Review
- Extracellular Vesicle fromInternational journal of molecular sciences · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
13 authors.
Funding
Abstract
Inflammatory diseases remain a major clinical challenge due to their complex pathologies and the limitations of current anti-inflammatory therapies. Conventional treatments, such as non-steroidal anti-inflammatory drugs and biologics, often provide incomplete relief and cause significant side effects, creating an urgent need for safer, more effective interventions. Plant-derived extracellular vesicles (PDEVs)-natural nanocarriers with inherent biocompatibility and cross-kingdom regulatory capacity-have emerged as a novel therapeutic approach that could address these shortcomings by safely delivering anti-inflammatory signals across species boundaries. This review examines PDEVs as both therapeutic tools and targets in inflammatory diseases, delineating their unique properties, anti-inflammatory mechanisms, and translational potential. Key topics include the biogenesis, composition, and isolation of PDEVs; their multifaceted roles in modulating immune responses; and evidence of efficacy in various models of inflammatory disease. Collectively, current findings indicate that PDEVs represent biocompatible, multi-target agents that effectively attenuate inflammation and promote tissue repair by overcoming the barriers to drug delivery and toxicity limitations of conventional therapies. Ongoing advances in omics technologies and bioengineering are expected to advance the characterization and engineering of PDEVs, fostering their integration into precision medicine approaches. Addressing challenges such as large-scale manufacturing, targeting specificity, and regulatory standardization will be crucial for translating PDEVs into safe, personalized anti-inflammatory therapies.
Indexed as
Identifiers
What Socratic holds
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 Socratic graph.