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Oncolytic viruses sensitize human tumor cells for NY-ESO-1 tumor antigen recognition by CD4+ effector T cells

Title: Oncolytic viruses sensitize human tumor cells for NY-ESO-1 tumor antigen recognition by CD4+ effector T cells
Authors: Delaunay, T.; Violland, M.; Boisgerault, N.; Dutoit, S.; Vignard, V.; Munz, C.; Gannage, M.; Dreno, B.; Vaivode, K.; Pjanova, D.; Labarriere, N.; Wang, Y.; Chiocca, E. A.; Boeuf, F. L.; Bell, J. C.; Erbs, P.; Tangy, F.; Gregoire, M.; Fonteneau, J. F.
Publication Year: 2018
Collection: Université de Lausanne (UNIL): Serval - Serveur académique lausannois
Subject Terms: CD4+ T Lymphocytes; Melanoma; Oncolytic Viruses; Oncolytic immunotherapy; Tumor-Associated Antigens
Description: Oncolytic immunotherapy using oncolytic viruses (OV) has been shown to stimulate the antitumor immune response by inducing the release of tumor-associated antigens (TAA) and danger signals from the dying infected tumor cells. In this study, we sought to determine if the lysis of tumor cells induced by different OV: measles virus, vaccinia virus, vesicular stomatitis virus, herpes simplex type I virus, adenovirus or enterovirus, has consequences on the capacity of tumor cells to present TAA, such as NY-ESO-1. We show that the co-culture of NY-ESO-1(neg)/HLA-DP4(pos) melanoma cells with NY-ESO-1(pos)/HLA-DP4(neg) melanoma cells infected and killed by different OV induces an intercellular transfer of NY-ESO-1 that allows the recognition of NY-ESO-1(neg)/HLA-DP4(pos) tumor cells by an HLA-DP4/NY-ESO-1(157-170)-specific CD4+ cytotoxic T cell clone, NY67. We then confirmed this result in a second model with an HLA-DP4+ melanoma cell line that expresses a low amount of NY-ESO-1. Recognition of this cell line by the NY67 clone is largely increased in the presence of OV productive infection. Altogether, our results show for the first time another mechanism of stimulation of the anti-tumor immune response by OV, via the loading of tumor cells with TAA that sensitizes them for direct recognition by specific effector CD4+ T cells, supporting the use of OV for cancer immunotherapy.
Document Type: article in journal/newspaper
Language: English
ISSN: 2162-4011; 29399408
Relation: OncoImmunology; https://iris.unil.ch/handle/iris/151465; serval:BIB_91BBDC9BC54E
DOI: 10.1080/2162402X.2017.1407897
Availability: https://iris.unil.ch/handle/iris/151465; https://doi.org/10.1080/2162402X.2017.1407897
Accession Number: edsbas.5243F590
Database: BASE