» Articles » PMID: 36203609

Circulating CD81-expressing Extracellular Vesicles As Biomarkers of Response for Immune-checkpoint Inhibitors in Advanced NSCLC

Abstract

PD-L1 in tumor cells is the only used biomarker for anti PD1/PD-L1 immune-checkpoints inhibitors (ICI) in Non Small Cell Lung Cancer (NSCLC) patients. However, this parameter is inaccurate to predict response, especially in patients with low tumor PD-L1. Here, we evaluated circulating EVs as possible biomarkers for ICI in advanced NSCLC patients with low tumoral PD-L1. EVs were isolated from plasma of 64 PD-L1 low, ICI-treated NSCLC patients, classified either as responders (R; complete or partial response by RECIST 1.1) or non-responders (NR). EVs were characterized following MISEV guidelines and by flow cytometry. T cells from healthy donors were triggered using patients' EVs. Unsupervised statistical approach was applied to correlate EVs' and patients' features to clinical response. R-EVs showed higher levels of tetraspanins (CD9, CD81, CD63) than NR-EVs, significantly associated to better overall response rate (ORR). In multivariable analysis CD81-EVs correlated with ORR. Unsupervised analysis revealed a cluster of variables on EVs, including tetraspanins, significantly associated with ORR and improved survival. R-EVs expressed more costimulatory molecules than NR-EVs although both increased T cell proliferation and partially, activation. Tetraspanins levels on EVs could represent promising biomarkers for ICI response in NSCLC.

Citing Articles

New insights into immune cells in cancer immunotherapy: from epigenetic modification, metabolic modulation to cell communication.

Qin S, Xie B, Wang Q, Yang R, Sun J, Hu C MedComm (2020). 2024; 5(6):e551.

PMID: 38783893 PMC: 11112485. DOI: 10.1002/mco2.551.


PD-L1 on large extracellular vesicles is a predictive biomarker for therapy response in tissue PD-L1-low and -negative patients with non-small cell lung cancer.

Schone N, Kemper M, Menck K, Evers G, Krekeler C, Schulze A J Extracell Vesicles. 2024; 13(3):e12418.

PMID: 38453684 PMC: 10920108. DOI: 10.1002/jev2.12418.


Impact of Immune Cells on Stroke Limited to Specific Subtypes: Evidence from Mendelian Randomization Study.

Chen C, Liu Q, Li Y, Yu J, Wang S, Liu L Neurol Ther. 2024; 13(3):599-609.

PMID: 38446379 PMC: 11136920. DOI: 10.1007/s40120-024-00592-y.


Biomarkers for Immune Checkpoint Inhibitor Response in NSCLC: Current Developments and Applicability.

Tostes K, Siqueira A, Reis R, Leal L, Arantes L Int J Mol Sci. 2023; 24(15).

PMID: 37569262 PMC: 10418476. DOI: 10.3390/ijms241511887.


Evaluating tumor cell- and T cell-derived extracellular vesicles as potential biomarkers of cancer and immune cell competence.

Whiteside T Expert Rev Mol Diagn. 2023; 23(2):109-122.

PMID: 36787282 PMC: 9998373. DOI: 10.1080/14737159.2023.2178902.

References
1.
Serrati S, Guida M, Di Fonte R, De Summa S, Strippoli S, Iacobazzi R . Circulating extracellular vesicles expressing PD1 and PD-L1 predict response and mediate resistance to checkpoint inhibitors immunotherapy in metastatic melanoma. Mol Cancer. 2022; 21(1):20. PMC: 8764806. DOI: 10.1186/s12943-021-01490-9. View

2.
Antonia S, Villegas A, Daniel D, Vicente D, Murakami S, Hui R . Durvalumab after Chemoradiotherapy in Stage III Non-Small-Cell Lung Cancer. N Engl J Med. 2017; 377(20):1919-1929. DOI: 10.1056/NEJMoa1709937. View

3.
Robbins P, Morelli A . Regulation of immune responses by extracellular vesicles. Nat Rev Immunol. 2014; 14(3):195-208. PMC: 4350779. DOI: 10.1038/nri3622. View

4.
Niemeijer A, Sahba S, Smit E, Lissenberg-Witte B, de Langen A, Thunnissen E . Association of tumour and stroma PD-1, PD-L1, CD3, CD4 and CD8 expression with DCB and OS to nivolumab treatment in NSCLC patients pre-treated with chemotherapy. Br J Cancer. 2020; 123(3):392-402. PMC: 7403301. DOI: 10.1038/s41416-020-0888-5. View

5.
Chalmin F, Ladoire S, Mignot G, Vincent J, Bruchard M, Remy-Martin J . Membrane-associated Hsp72 from tumor-derived exosomes mediates STAT3-dependent immunosuppressive function of mouse and human myeloid-derived suppressor cells. J Clin Invest. 2010; 120(2):457-71. PMC: 2810085. DOI: 10.1172/JCI40483. View