ReviewNanomedicine (London, England)2025
Emerging gene delivery nanosystems for the treatment of acute lung injury.
Review in Nanomedicine (London, England), 2025. 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.
- Scavenger receptor-mediated lung-targeted delivery of anti-miR-155 oligoDNA nanomicelles with curcumin for acute lung injury therapy.Asian journal of pharmaceutical sciences · 2026Article
- Advances in natural product-based nanoparticles for the treatment of acute lung injury.Materials today. Bio · 2025Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Acute lung injury (ALI) is an inflammatory phenomenon characterized by hypoxia and edema. When the lungs are damaged, inflammation begins due to pro-inflammatory cytokines secreted by macrophages in the alveoli. In addition, neutrophils infiltrate the lung tissue, inducing additional inflammation. Accumulation of plasma proteins and fluids in the alveoli causes severe hypoxia and respiratory failure. Current treatments include anti-inflammatory drugs such as steroids and mechanical ventilation; however, these treatments have transient effects and may be accompanied by significant deleterious side effects, increasing mortality rate. This suggests that new therapeutic modalities should be developed for effective treatment of ALI. Recently, gene therapy for ALI was proposed as a novel treatment for ALI. Therapeutic genes such as anti-inflammatory genes and siRNAs/miRNAs have been evaluated for suppression of inflammatory reactions. The results have indicated that efficient carriers for gene delivery need to be developed. Various nanosystems for delivery of therapeutic genes to the lungs, including polymers, lipid nanoparticles, exosomes, and cell membrane-based nanovesicles, have been investigated. In this review, an in-depth analysis of gene delivery nanosystems for ALI treatment is presented with major achievements and challenges for future development. PubMed and Google Scholar were used as resources for searching related literature.
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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.