Tumor-Infiltrating T Cells and Their Exosomes: Functional Roles and Microenvironmental Impact
DOI: 10.23977/tranc.2025.060110 | Downloads: 4 | Views: 878
Author(s)
Xingyu Chen 1, Yulan Fan 2, Xinyu Li 3
Affiliation(s)
1 Cranleigh School, Horseshoe Ln, Cranleigh GU6 8QQ, UK
2 RDF International School, Bai Zi Yuan Science and Technology Park, Kunan Road, Dapeng Street, Dapeng New District, Shenzhen City, Guangdong Province, China
3 Shenzhen Senior High School, No. 8, Zetian Road, Xiangmihu Street, Futian District, Shenzhen City, Guangdong Province, China
Corresponding Author
Xingyu ChenABSTRACT
Exosomes are nanosized phospholipid bilayer vesicles secreted by various cells, rich in bioactive molecules such as proteins, nucleic acids and lipids, which play important roles in intercellular communication and microenvironmental regulation. In recent years, T cell-derived exosomes have become a hotspot in tumor immunity research due to their immune specificity and functional diversity. The aim of this study was to systematically analyze the physicochemical properties of T cell-derived exosomes and their functional effects on tumor cells. T cell-derived exosomes were activated and isolated in vitro, and their particle size distribution, marker protein expression and cellular uptake ability were verified by nanoparticle tracking analysis, Western blot and confocal imaging. Functional experiments showed that T-cell exosomes can effectively inhibit tumor cell proliferation and induce apoptosis, suggesting that they have potential anti-tumor activity. This study provides experimental basis and theoretical support for the application of T-cell exosomes in tumor immunotherapy and expands its research horizons in the field of precision medicine.
KEYWORDS
T Cell, T Cell Exosome, Tumor ImmunotherapyCITE THIS PAPER
Xingyu Chen, Yulan Fan, Xinyu Li, Tumor-Infiltrating T Cells and Their Exosomes: Functional Roles and Microenvironmental Impact. Transactions on Cancer (2025) Vol. 6: 71-86. DOI: http://dx.doi.org/10.23977/tranc.2025.060110.
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