Author:
Signorelli Diego,Ghidotti Patrizia,Proto Claudia,Brambilla Marta,De Toma Alessandro,Ferrara Roberto,Galli Giulia,Ganzinelli Monica,Lo Russo Giuseppe,Prelaj Arsela,Occhipinti Mario,Viscardi Giuseppe,Capizzuto Valentina,Pontis Francesca,Petraroia Ilaria,Ferretti Anna Maria,Colombo Mario Paolo,Torri Valter,Sozzi Gabriella,Garassino Marina Chiara,Jachetti Elena,Fortunato Orazio
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 in vitro 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.
Subject
Immunology,Immunology and Allergy
Cited by
6 articles.
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