Author
Listed:
- Guohao Wang
(University of Macau
University of Macau)
- Lisi Xie
(University of Macau
University of Macau)
- Bei Li
(University of Macau
University of Macau)
- Wei Sang
(University of Macau
University of Macau)
- Jie Yan
(University of Macau
University of Macau)
- Jie Li
(University of Macau
University of Macau)
- Hao Tian
(University of Macau
University of Macau)
- Wenxi Li
(University of Macau
University of Macau)
- Zhan Zhang
(University of Macau
University of Macau)
- Ye Tian
(University of Macau
University of Macau)
- Yunlu Dai
(University of Macau
University of Macau
University of Macau)
Abstract
In addition to increasing the expression of programmed death-ligand 1 (PD-L1), tumor cells can also secrete exosomal PD-L1 to suppress T cell activity. Emerging evidence has revealed that exosomal PD-L1 resists immune checkpoint blockade, and may contribute to resistance to therapy. In this scenario, suppressing the secretion of tumor-derived exosomes may aid therapy. Here, we develop an assembly of exosome inhibitor (GW4869) and ferroptosis inducer (Fe3+) via amphiphilic hyaluronic acid. Cooperation between the two active components in the constructed nanounit induces an anti-tumor immunoresponse to B16F10 melanoma cells and stimulates cytotoxic T lymphocytes and immunological memory. The nanounit enhances the response to PD-L1 checkpoint blockade and may represent a therapeutic strategy for enhancing the response to this therapy.
Suggested Citation
Guohao Wang & Lisi Xie & Bei Li & Wei Sang & Jie Yan & Jie Li & Hao Tian & Wenxi Li & Zhan Zhang & Ye Tian & Yunlu Dai, 2021.
"A nanounit strategy reverses immune suppression of exosomal PD-L1 and is associated with enhanced ferroptosis,"
Nature Communications, Nature, vol. 12(1), pages 1-12, December.
Handle:
RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-25990-w
DOI: 10.1038/s41467-021-25990-w
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