Identification and Immunogenicity of African Swine Fever Virus Antigens.
Adenoviridae
/ immunology
African Swine Fever
/ immunology
African Swine Fever Virus
/ immunology
Animals
Antigens, Viral
/ immunology
CD8-Positive T-Lymphocytes
/ immunology
Genetic Vectors
/ immunology
Immunity, Cellular
/ immunology
Immunity, Humoral
/ immunology
Immunization
/ methods
Swine
Vaccination
/ methods
Viral Proteins
/ immunology
Viral Vaccines
/ immunology
Viremia
/ immunology
Virulence
/ immunology
African swine fever (virus)
ELISPOT assay for interferon gamma
T-cell
antigen presentation
disease enhancement
swine
viral replication
Journal
Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960
Informations de publication
Date de publication:
2019
2019
Historique:
received:
31
10
2018
accepted:
23
05
2019
entrez:
6
7
2019
pubmed:
6
7
2019
medline:
23
10
2020
Statut:
epublish
Résumé
African swine fever (ASF) is a lethal haemorrhagic disease of domestic pigs for which there is no vaccine. Strains of the virus with reduced virulence can provide protection against related virulent strains of ASFV, but protection is not 100% and there are concerns about the safety profile of such viruses. However, they provide a useful tool for understanding the immune response to ASFV and previous studies using the low virulent isolate OUR T88/3 have shown that CD8+ cells are crucial for protection. In order to develop a vaccine that stimulates an effective anti-ASFV T-cell response we need to know which of the >150 viral proteins are recognized by the cellular immune response. Therefore, we used a gamma interferon ELIspot assay to screen for viral proteins recognized by lymphocytes from ASF-immune pigs using peptides corresponding to 133 proteins predicted to be encoded by OUR T88/3. Eighteen antigens that were recognized by ASFV-specific lymphocytes were then incorporated into adenovirus and MVA vectors, which were used in immunization and challenge experiments in pigs. We present a systematic characterization of the cellular immune response to this devastating disease and identify proteins capable of inducing ASFV-specific cellular and humoral immune responses in pigs. Pools of viral vectors expressing these genes did not protect animals from severe disease, but did reduce viremia in a proportion of pigs following ASFV challenge.
Identifiants
pubmed: 31275307
doi: 10.3389/fimmu.2019.01318
pmc: PMC6593957
doi:
Substances chimiques
Antigens, Viral
0
Viral Proteins
0
Viral Vaccines
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1318Subventions
Organisme : Biotechnology and Biological Sciences Research Council
ID : BBS/E/I/00007036
Pays : United Kingdom
Organisme : Biotechnology and Biological Sciences Research Council
ID : BBS/E/I/00007031
Pays : United Kingdom
Organisme : Biotechnology and Biological Sciences Research Council
ID : BBS/E/I/00007039
Pays : United Kingdom
Organisme : Biotechnology and Biological Sciences Research Council
ID : BBS/E/I/00007038
Pays : United Kingdom
Organisme : Biotechnology and Biological Sciences Research Council
ID : BBS/E/I/00007037
Pays : United Kingdom
Organisme : Biotechnology and Biological Sciences Research Council
ID : BBS/E/I/00007034
Pays : United Kingdom
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