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Extracellular vesicle PD-L1 in reshaping tumor immune microenvironment: biological function and potential therapy
Jiaxing Liu1, Xueqiang Peng1, Shuo Yang1
1Department of General Surgery, The Fourth Affiliated Hospital, China Medical University, Shenyang, 110032, China.
Abstract:
Programmed cell death 1 ligand 1 (PD-L1) is the ligand for programmed death protein-1 (PD-1), is associated with immunosuppression. Signaling via PD-1/PD-L1 will transmits negative regulatory signals to T cells, inducing T-cell inhibition, reducing CD8+ T-cell proliferation, or promoting T-cell apoptosis, which effectively reduces the immune response and leads to large-scale tumor growth. Accordingly, many antibody preparations targeting PD-1 or PD-L1 have been designed to block the binding of these two proteins and restore T-cell proliferation and cytotoxicity of T cells. However, these drugs are ineffective in clinical practice. Recently, numerous of studies have shown that, in addition to the surface of tumor cells, PD-L1 is also found on the surface of extracellular vesicles secreted by these cells. Extracellular vesicle PD-L1 can also interact with PD-1 on the surface of T cells, leading to immunosuppression, and has been proposed as a potential mechanism underlying PD-1/PD-L1-targeted drug resistance. Therefore, it is important to explore the production, regulation and tumor immunosuppression of PD-L1 on the surface of tumor cells and extracellular vesicles, as well as the potential clinical application of extracellular vesicle PD-L1 as tumor biomarkers and therapeutic targets. Video Abstract.
Insights
Programmed cell death 1 ligand 1 (PD-L1) on tumor cells and extracellular vesicles suppresses T-cell immunity. Targeting PD-L1 may overcome resistance to current immunotherapies, offering new diagnostic and therapeutic strategies.
Area of Science:
- Immunology
- Cancer Biology
- Cell Biology
Background:
- Programmed cell death 1 ligand 1 (PD-L1) binding to PD-1 inhibits T cells, promoting tumor growth.
- Current PD-1/PD-L1 therapies often face clinical resistance.
- PD-L1 is also expressed on extracellular vesicles (EVs) secreted by tumor cells.
Purpose of the Study:
- Investigate the role of PD-L1 on tumor cells and EVs in immune suppression.
- Explore mechanisms of PD-1/PD-L1 targeted drug resistance.
- Evaluate EV PD-L1 as a biomarker and therapeutic target.
Main Methods:
- Review of existing studies on PD-L1 expression and function.
- Analysis of PD-L1 interaction with PD-1 on T cells.
- Discussion of EV PD-L1's role in immunosuppression and drug resistance.
Main Results:
- PD-L1 on both tumor cells and EVs mediates immunosuppression by inhibiting T cells.
- EV PD-L1 is a potential mechanism for resistance to PD-1/PD-L1 therapies.
- EV PD-L1 presents opportunities for novel diagnostic and therapeutic approaches.
Conclusions:
- Understanding EV PD-L1 is crucial for improving cancer immunotherapy.
- Targeting EV PD-L1 could enhance anti-tumor immune responses.
- EV PD-L1 holds promise as a biomarker and therapeutic target in oncology.
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