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In Vivo Immunogenicity Screening of Tumor-Derived Extracellular Vesicles by Flow Cytometry of Splenic T Cells
Published on: September 23, 2021
Murine Leukemia-Derived Extracellular Vesicles Elicit Antitumor Immune Response
Alejandro Pando1, Loren Fast1, Patrycja M Dubielecka1
1Division of Hematology/Oncology, Department of Medicine, Rhode Island Hospital and the Warren Alpert School of Medicine at Brown University, Providence, RI, USA.
Leukemia-derived extracellular vesicles (EVs) stimulate T cell responses, enhancing anti-leukemia immunity in vitro and in vivo. These findings suggest EVs can be used to boost anti-cancer immune responses.
Area of Science:
- Immunology
- Cancer Biology
- Cell Biology
Background:
- Extracellular vesicles (EVs) are cell-secreted particles with immunomodulatory potential.
- Cancer-derived EVs can promote tumor growth or be used for anti-cancer therapies.
Purpose of the Study:
- To investigate the immunomodulatory effects of extracellular vesicles (EVs) from acute myeloid leukemia (AML) cells.
- To assess the potential of AML-derived EVs in enhancing anti-leukemia immune responses.
Main Methods:
- Isolation of extracellular vesicles (EVs) from the murine AML cell line C1498.
- Evaluation of EV effects on T cell proliferation and cytolytic activity in vitro.
- Assessment of T cell responses in vivo following EV injection into mice.
Main Results:
- Leukemia-derived EVs increased CD3+ T cell proliferation and enhanced their cytolytic activity against leukemia cells in vitro.
- In vivo administration of EVs induced T cell responses and improved immune responses upon re-stimulation.
- EVs demonstrated immunomodulatory effects on cell-mediated immunity.
Conclusions:
- Extracellular vesicles (EVs) derived from C1498 AML cells exhibit significant immunomodulatory effects.
- These EVs can enhance cell-mediated immune responses against leukemia.
- AML-derived EVs hold potential for developing novel anti-leukemia immunotherapies.
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