Back to Search
Start Over
Immunogenic particles with a broad antigenic spectrum stimulate cytolytic T cells and offer increased protection against EBV infection ex vivo and in mice
- 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.
- Subjects :
- 0301 basic medicine
Epstein-Barr Virus Infections
Herpesvirus 4, Human
B Cells
Physiology
medicine.disease_cause
Biochemistry
Mice
White Blood Cells
0302 clinical medicine
Spectrum Analysis Techniques
Animal Cells
[SDV.MHEP.MI]Life Sciences [q-bio]/Human health and pathology/Infectious diseases
Immune Physiology
hemic and lymphatic diseases
Virus latency
Medicine and Health Sciences
Cytotoxic T cell
Public and Occupational Health
Biology (General)
Antigens, Viral
Pathology and laboratory medicine
Immune System Proteins
T Cells
Medical microbiology
Flow Cytometry
Vaccination and Immunization
3. Good health
Virus Latency
Lytic cycle
Spectrophotometry
Viruses
[SDV.MHEP.MI] Life Sciences [q-bio]/Human health and pathology/Infectious diseases
[SDV.IMM]Life Sciences [q-bio]/Immunology
Cytophotometry
Cellular Types
Pathogens
Research Article
Herpesviruses
[SDV.IMM] Life Sciences [q-bio]/Immunology
QH301-705.5
Immune Cells
Immunology
Cytotoxic T cells
Herpesvirus Vaccines
Biology
Research and Analysis Methods
Microbiology
Virus
Antibodies
03 medical and health sciences
Immune system
Antigen
Virology
Genetics
medicine
Animals
Epstein-Barr virus
Antigens
Antibody-Producing Cells
Molecular Biology
Blood Cells
Organisms
Viral pathogens
Biology and Life Sciences
Proteins
Cell Biology
RC581-607
medicine.disease
Epstein–Barr virus
Microbial pathogens
030104 developmental biology
Humanized mouse
Parasitology
Preventive Medicine
Immunologic diseases. Allergy
DNA viruses
030215 immunology
T-Lymphocytes, Cytotoxic
Subjects
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