ReviewBioactive materials2025
Advanced nanotherapies for precision treatment of inflammatory lung diseases.
Review in Bioactive materials, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 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
6 citing papers in PubMed.
- Inhalable PD-L1-engineered hybrid cellular vesicles suppress excessive neutrophil activation and restore mitochondrial homeostasis to alleviate ischemia-reperfusion lung injury and pneumonia.Bioactive materials · 2026Article
- Pulmonary Drug Delivery in the Era of Nanomedicine: From Biological Barriers to Artificial Intelligence-Driven Optimization.Pharmaceuticals (Basel, Switzerland) · 2026Review
- Engineering a macromolecular JAK inhibitor for treating acute inflammation and endotoxaemia.Nature biomedical engineering · 2026Article
- Inflammation-triggered self-immolative conjugates enable oral peptide delivery by overcoming gastrointestinal barriers.Science advances · 2026Article
- miRNAs-neutrophil axis: novel insights into acute lung injury and chronic inflammatory lung diseases.Frontiers in immunology · 2026Review
- Targeting the Aryl Hydrocarbon Receptor: The Potential of Indole Compounds in the Treatment of Cystic Fibrosis.International journal of molecular sciences · 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
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Inflammatory lung diseases, particularly those associated with acute pulmonary inflammation, represent a major clinical challenge due to their high global morbidity and mortality rates, as well as the absence of effective and safe therapies. While traditional pharmacological interventions have been frequently used for managing acute inflammatory lung diseases, novel therapeutic strategies are urgently needed to improve clinical outcomes. Recently, advanced nanotherapies have emerged as a promising paradigm for targeted treatment of inflammatory lung diseases, leveraging the unique pathophysiological features of acute pulmonary inflammation, characterized by excessive inflammatory mediator production and robust immune cell infiltration. This review first outlines the pathogenic mechanisms and pathological microenvironment linked with acute lung inflammation. Then different bioresponsive nanocarriers are comprehensively summarized and discussed, with a particular emphasis on inflammation-responsive nanotherapies engineered for modulating acute pulmonary inflammation. Furthermore, innovative biomimetic nanotherapies, such as those based on cell hitchhiking, cell membrane coating, and extracellular vesicles, are critically examined. Finally, we highlight the key challenges impeding the clinical translation of these next-generation nanotherapies for acute lung inflammation and propose potential avenues for future research.
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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.