EGFR Mutation and TKI Treatment Promote Secretion of Small Extracellular Vesicle PD-L1 and Contribute to Immunosuppression in NSCLC

• Published in: Biomolecules (Basel, Switzerland) Switzerland), 2024-07, Vol.14 (7), p.820
• Main Authors: Liu, Hai-Ming, Yu, Zi-Li, Xia, Hou-Fu, Zhang, Lin-Zhou, Fu, Qiu-Yun, Wang, Yi, Gong, Hong-Yun, Chen, Gang
• Format: Article
• Language: English
• Subjects: Cancer therapies; CD8 antigen; EGFR-mutant NSCLC; Enzyme-linked immunosorbent assay; Epidermal growth factor receptors; Extracellular vesicles; Flow cytometry; Immunosuppression; Immunotherapy; Kinases; Lymphocytes T; Molecular modelling; Mutation; Nanoparticles; Non-small cell lung carcinoma; PD-1 protein; PD-L1 protein; Proteins; sEV PD-L1; Small cell lung carcinoma; Software; TKIs; Tumor cell lines; Tumor cells; Tumors; Tyrosine kinase inhibitors; Western blotting
• ISSN: 2218-273X; 2218-273X
• DOI: 10.3390/biom14070820

In Asian populations with non-small-cell lung cancer (NSCLC), mutations are highly prevalent, occurring in roughly half of these patients. Studies have revealed that individuals with mutation typically fare worse with immunotherapy. In patients who received EGFR tyrosine kinase inhibitor (TKI) treatment followed by anti-PD-1 therapy, poor results were observed. The underlying mechanism remains unclear. We used high-resolution flow cytometry and ELISA to detect the circulating level of small extracellular vesicle (sEV) PD-L1 in NSCLC individuals with mutations before and after receiving TKIs. The secretion amount of sEV PD-L1 of lung cancer cell lines with mutations under TKI treatment or not were detected using high-resolution flow cytometry and Western blotting. The results revealed that patients harboring mutations exhibit increased levels of sEV PD-L1 in circulation, which inversely correlated with the presence of CD8 T cells in tumor tissues. Furthermore, tumor cells carrying mutations secrete a higher quantity of PD-L1-positive sEVs. TKI treatment appeared to amplify the levels of PD-L1-positive sEVs in the bloodstream. Mutation-induced and TKI-induced sEVs substantially impaired the functionality of CD8 T cells. Importantly, our findings indicated that mutations and TKI therapies promote secretion of PD-L1-positive sEVs via distinct molecular mechanisms, namely the HRS and ALIX pathways, respectively. In conclusion, the increased secretion of PD-L1-positive sEVs, prompted by genetic alterations and TKI administration, may contribute to the limited efficacy of immunotherapy observed in -mutant patients and patients who have received TKI treatment.