Keratinocyte differentiation antigen-specific T cells in immune checkpoint inhibitor-treated NSCLC patients are associated with improved survival.
Détails
Télécharger: 34858733_BIB_F7C830C8D442.pdf (1269.29 [Ko])
Etat: Public
Version: Final published version
Licence: CC BY-NC 4.0
Etat: Public
Version: Final published version
Licence: CC BY-NC 4.0
ID Serval
serval:BIB_F7C830C8D442
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Keratinocyte differentiation antigen-specific T cells in immune checkpoint inhibitor-treated NSCLC patients are associated with improved survival.
Périodique
Oncoimmunology
ISSN
2162-402X (Electronic)
ISSN-L
2162-4011
Statut éditorial
Publié
Date de publication
2021
Peer-reviewed
Oui
Volume
10
Numéro
1
Pages
2006893
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: epublish
Publication Status: epublish
Résumé
Immune checkpoint inhibitors (ICIs) have improved the survival of patients with non-small cell lung cancer (NSCLC) by reinvigorating tumor-specific T cell responses. However, the specificity of such T cells and the human leukocyte antigen (HLA)-associated epitopes recognized, remain elusive. In this study, we identified NSCLC T cell epitopes of recently described NSCLC-associated antigens, termed keratinocyte differentiation antigens. Epitopes of these antigens were presented by HLA-A 03:01 and HLA-C 04:01 and were associated with responses to ICI therapy. Patients with CD8 <sup>+</sup> T cell responses to these epitopes had improved overall and progression-free survival. T cells specific for such epitopes could eliminate HLA class I-matched NSCLC cells ex vivo and were enriched in patient lung tumors. The identification of novel lung cancer HLA-associated epitopes that correlate with improved ICI-dependent treatment outcomes suggests that keratinocyte-specific proteins are important tumor-associated antigens in NSCLC. These findings improve our understanding of the mechanisms of ICI therapy and may help support the development of vaccination strategies to improve ICI-based treatment of these tumors.
Mots-clé
Antigens, Differentiation/therapeutic use, Carcinoma, Non-Small-Cell Lung/drug therapy, Humans, Immune Checkpoint Inhibitors, Keratinocytes, Lung Neoplasms/drug therapy, Immune checkpoint inhibitor therapy, NSCLC, autoimmune toxicity, tumor-associated antigen
Pubmed
Web of science
Open Access
Oui
Financement(s)
Fonds national suisse
Fondation Novartis
Création de la notice
03/12/2021 18:46
Dernière modification de la notice
23/11/2022 7:17