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Updated: Nov 3, 2025

In Vivo Immunogenicity Screening of Tumor-Derived Extracellular Vesicles by Flow Cytometry of Splenic T Cells
Published on: September 23, 2021
Immunology of Cell Death in Cancer Immunotherapy
Lorenzo Galluzzi1,2,3,4,5, Abhishek D Garg6
1Department of Radiation Oncology, Weill Cornell Medical College, New York, NY 10065, USA.
Abstract:
Over the last two decades, a large volume of studies has established that dying and dead cancer cells exert a potent immunomodulatory effect on their immediate microenvironment, which has a major influence on the anticancer immunity [...].
Insights
Dying and dead cancer cells significantly impact the tumor microenvironment and anticancer immunity. Understanding these effects is crucial for developing effective cancer immunotherapies.
Area of Science:
- Immunology
- Oncology
- Cell Biology
Background:
- Accumulating evidence over 20 years highlights the immunomodulatory role of dying and dead cancer cells.
- These cellular remnants profoundly influence the tumor microenvironment (TME).
- This influence significantly shapes the host's anticancer immune responses.
Discussion:
- The immunomodulatory effects of cancer cell death are complex and context-dependent.
- These effects can be both pro-tumorigenic and anti-tumorigenic.
- Key mechanisms involve the release of damage-associated molecular patterns (DAMPs) and altered cytokine profiles.
Key Insights:
- Cancer cell death is not merely a passive event but an active modulator of anti-cancer immunity.
- The TME's response to dying cancer cells dictates the efficacy of immunotherapies.
- Targeting cancer cell death pathways offers novel therapeutic strategies.
Outlook:
- Further research is needed to fully elucidate the intricate crosstalk between cancer cell death and immune cells.
- Harnessing the immunomodulatory potential of cancer cell death could lead to more effective cancer treatments.
- Developing strategies to control the immunomodulatory consequences of cell death is a promising avenue for cancer immunotherapy.
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