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Immunogenic particles with a broad antigenic spectrum stimulate cytolytic T cells and offer increased protection against EBV infection ex vivo and in mice

Authors :
Ming Han Tsai
Dwain G. van Zyl
Viktor Schneidt
Henri Jacques Delecluse
Anatoliy Shumilov
Herbert Fluhr
Josef Mautner
B. Schlehe
Remy Poirey
Unit F100 [Heidelberg, Allemagne]
German Cancer Research Center - Deutsches Krebsforschungszentrum [Heidelberg] (DKFZ)
Faculty of Biosciences [Heidelberg, Allemagne]
Heidelberg University
Microbiology and infectious diseases
German Cancer Research Center - Deutsches Krebsforschungszentrum [Heidelberg] (DKFZ)-Institut National de la Santé et de la Recherche Médicale (INSERM)
German Center for Infection Research - partner site Hannover-Braunschweig (DZIF)
Frauenklinik [Heidelberg, Allemagne]
Heidelberg University Hospital [Heidelberg]
Children's Hospital [Munich, Allemagne]
Helmholtz-Zentrum München (HZM)-Technische Universität Munchen - Université Technique de Munich [Munich, Allemagne] (TUM)
Funding has been received from the German Cancer Research Center (Project number F100), Inserm (Project number U1074) and Deutsche Krebshilfe (70110621).
Technische Universität Munchen - Université Technique de Munich [Munich, Allemagne] (TUM)-Helmholtz Zentrum München = German Research Center for Environmental Health
Bodescot, Myriam
Source :
PLoS Pathogens, PLoS Pathogens, Public Library of Science, 2018, 14 (12), pp.e1007464. ⟨10.1371/journal.ppat.1007464⟩, PLoS Pathog. 14:e1007464 (2018), PLoS Pathogens, Vol 14, Iss 12, p e1007464 (2018)
Publication Year :
2018
Publisher :
HAL CCSD, 2018.

Abstract

The ubiquitous Epstein-Barr virus (EBV) is the primary cause of infectious mononucleosis and is etiologically linked to the development of several malignancies and autoimmune diseases. EBV has a multifaceted life cycle that comprises virus lytic replication and latency programs. Considering EBV infection holistically, we rationalized that prophylactic EBV vaccines should ideally prime the immune system against lytic and latent proteins. To this end, we generated highly immunogenic particles that contain antigens from both these cycles. In addition to stimulating EBV-specific T cells that recognize lytic or latent proteins, we show that the immunogenic particles enable the ex vivo expansion of cytolytic EBV-specific T cells that efficiently control EBV-infected B cells, preventing their outgrowth. Lastly, we show that immunogenic particles containing the latent protein EBNA1 afford significant protection against wild-type EBV in a humanized mouse model. Vaccines that include antigens which predominate throughout the EBV life cycle are likely to enhance their ability to protect against EBV infection.<br />Author summary Human herpesviruses are tremendously successful pathogens that establish lifelong infection in a substantial proportion of the population. The oncogenic γ-herpesvirus EBV, like other herpesviruses, expresses a plethora of open-reading frames throughout its multifaceted life cycle. We have developed a prophylactic vaccine candidate in the form of immunogenic particles that contain several EBV antigens. This is in stark contrast to the vast majority of EBV vaccines candidates that contain only one or two EBV antigens. Our immunogenic particles were shown capable of stimulating several EBV-specific T-cell clones in vitro. The immunogenic particles were also capable of expanding cytolytic EBV-specific T cells ex vivo and provided a protective benefit in vivo when used as a prophylactic vaccine.

Details

Language :
English
ISSN :
15537366 and 15537374
Database :
OpenAIRE
Journal :
PLoS Pathogens, PLoS Pathogens, Public Library of Science, 2018, 14 (12), pp.e1007464. ⟨10.1371/journal.ppat.1007464⟩, PLoS Pathog. 14:e1007464 (2018), PLoS Pathogens, Vol 14, Iss 12, p e1007464 (2018)
Accession number :
edsair.doi.dedup.....a3c8bc5733de43ef9eabd0f941a24c3f