ReviewCancer immunology, immunotherapy : CII2025
T cell-derived small extracellular vesicles in cancer-immune interactions.
Review in Cancer immunology, immunotherapy : CII, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 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
4 citing papers in PubMed.
- Choosing the Right Extracellular Vesicle: Cross-Kingdom Immunological Functions Linking Molecular Mechanisms to Therapeutic Applications.Biomolecules · 2026Review
- T cell-inspired therapeutic delivery platforms: From nanomedicines to cell therapy.Materials today. Bio · 2026Review
- An updated review on the role of extracellular vesicles in immune system modulation in breast cancer with special emphasis on immune checkpoint regulators.Frontiers in immunology · 2026Review
- Engineering Biomimetic Nanoplatforms for Acute Lung Injury: From Mechanistic Insights to Translational Opportunities.International journal of nanomedicine · 2025Review
Corrections and comments
- Erratum issued
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Small extracellular vesicles (sEVs) are lipid-encapsulated nanoparticles released following the endocytic fusion of multivesicular bodies with the plasma membrane. sEVs are secreted by most eukaryotic cells, and they contain proteins, RNAs and DNA. They act primarily as mediators of intercellular communication through the transport of their contents from donor to recipient cells. Immune cells, including T cells, secrete sEVs following activation. T cell-derived sEVs (T-sEVs) have gained attention in cell-to-cell signalling and as promising immunotherapeutic agents. Growing evidence suggests that T-sEVs are key players in cancer immunotherapy responses. A better understanding of T-sEVs production and properties is key for grasping their biological functions. Extensive current literature on tumour-derived sEVs and their applications in diagnostics or therapeutics is in disconnect with fewer reports on T-sEVs. In this review, we discuss T-sEV biogenesis, their roles in cell-to-cell communication and potential applications in immunotherapy for cancer.
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Identifiers
What OpenQuestion 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 OpenQuestion graph.