Omics · study · 2026
Natural Killer Cell-Derived Extracellular Vesicles Reprogram Human Immunity to Enhance Tumour Cytotoxicity
Listed in NCBI GEO
Description
Despite evidence of natural killer cell–derived extracellular vesicles (NK-EVs) possessing intrinsic cytotoxicity, their broader immunomodulatory effects on human immune subsets remain poorly defined, representing a key knowledge gap that must be addressed to advance their clinical translation as cancer immunotherapeutics. In this study, the immunomodulatory effects of NK-EVs were evaluated on peripheral blood mononuclear cells (PBMCs), a mixed population of circulating immune cells, from healthy donors and patients with aggressive breast cancer.
NK-EVs were produced through a clinically scalable production process and PBMCs exposed to NK-EVs were assessed using high-resolution single-cell transcriptomics and functional cytotoxicity assays. NK-EVs reprogrammed PBMC on a transcriptomic (gene regulation) and cellular level, resulting in functional improvement of the PBMCs' tumour cell killing capabilities. These effects were mediated through distinct PBMC subsets, including cytotoxic T cells, NK cells and myeloid cells.
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Interestingly, CD8+ T cells, CD56+ NK cells, and CD33+ myeloid cells appear to play a more prominent role in NK-EV-mediated immune reprogramming than CD4+ T cells, with genes involved in their activation being markedly affected upon EV stimulation. Notably, the responses were consistent across all biological PBMC donors (n=6), regardless of disease status. Collectively, these findings demonstrate that NK-EVs orchestrate coordinated immune activation, highlighting their promise as an immunotherapeutic for cancer and other immune-mediated diseases.
Links
Get the data
- GEO FTP directory ftp.ncbi.nlm.nih.gov/geo/series/GSE309nnn/GSE309543 ↗
download · from NCBI GEO
Where it is published
- GEO accession page ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE309543 ↗
landing page · from NCBI GEO
Documentation and papers
- PRJNA1336236 ncbi.nlm.nih.gov/bioproject/PRJNA1336236 ↗
project · from NCBI GEO
- PubMed 42383255 pubmed.ncbi.nlm.nih.gov/42383255 ↗
publication · from NCBI GEO
Topics
- Stated by source
- Expression profiling by high throughput sequencing · Homo sapiens
- From keywords
- Life Sciences
Provenance · 1 source records, 9 field assertions
| Source | Key | Last seen | Raw |
|---|---|---|---|
| NCBI GEO | GSE309543 | 15 d ago | JSON v1 |
| Field | Assertion | Extractor | Evidence |
|---|---|---|---|
| access_level | source · NCBI GEO | connector:ncbi_geo@1.0.0 | |
| concepts[disease].local:disease:cancer | enrichment · NCBI GEO | keyword-concept-rules@1.0.0 | title+description (75%) |
| concepts[disease].local:disease:disease | enrichment · NCBI GEO | keyword-concept-rules@1.0.0 | title+description (75%) |
| concepts[field].local:field:life-sciences | mapping · NCBI GEO | connector:ncbi_geo@1.0.0 | |
| concepts[method].geo_series_type:expression-profiling-by-high-throughput-sequencing | source · NCBI GEO | connector:ncbi_geo@1.0.0 | /gdstype |
| concepts[organism].NCBITaxon:9606 | source · NCBI GEO | connector:ncbi_geo@1.0.0 | /taxon |
| description | source · NCBI GEO | connector:ncbi_geo@1.0.0 | /summary |
| publication_date | source · NCBI GEO | connector:ncbi_geo@1.0.0 | |
| title | source · NCBI GEO | connector:ncbi_geo@1.0.0 | /title |