Identification of HLA-A*11:01 and A*02:01-Restricted EBV Peptides Using HLA Peptidomics.
Humans
Herpesvirus 4, Human
/ immunology
Peptides
/ immunology
Epstein-Barr Virus Infections
/ immunology
HLA-A2 Antigen
/ immunology
Nasopharyngeal Carcinoma
/ immunology
HLA-A11 Antigen
/ immunology
Proteomics
/ methods
Nasopharyngeal Neoplasms
/ immunology
China
Tandem Mass Spectrometry
Epitopes, T-Lymphocyte
/ immunology
Cell Line, Tumor
Epstein-Barr Virus
HLA peptidomics
epitopes
nasopharyngeal carcinoma
Journal
Viruses
ISSN: 1999-4915
Titre abrégé: Viruses
Pays: Switzerland
ID NLM: 101509722
Informations de publication
Date de publication:
25 Apr 2024
25 Apr 2024
Historique:
received:
24
03
2024
revised:
19
04
2024
accepted:
23
04
2024
medline:
25
5
2024
pubmed:
25
5
2024
entrez:
25
5
2024
Statut:
epublish
Résumé
Epstein-Barr Virus (EBV) is closely linked to nasopharyngeal carcinoma (NPC), notably prevalent in southern China. Although type II latency of EBV plays a crucial role in the development of NPC, some lytic genes and intermittent reactivation are also critical for viral propagation and tumor progression. Since T cell-mediated immunity is effective in targeted killing of EBV-positive cells, it is important to identify EBV-derived peptides presented by highly prevalent human leukocyte antigen class I (HLA-I) molecules throughout the EBV life cycle. Here, we constructed an EBV-positive NPC cell model to evaluate the presentation of EBV lytic phase peptides on streptavidin-tagged specific HLA-I molecules. Utilizing a mass spectrometry (LC-MS/MS)-based immunopeptidomic approach, we characterized eleven novel EBV peptides as well as two previously identified peptides. Furthermore, we determined these peptides were immunogenic and could stimulate PBMCs from EBV VCA/NA-IgA positive donors in an NPC endemic southern Chinese population. Overall, this work demonstrates that highly prevalent HLA-I-specific EBV peptides can be captured and functionally presented to elicit immune responses in an in vitro model, which provides insight into the epitopes presented during EBV lytic cycle and reactivation. It expands the range of viral targets for potential NPC early diagnosis and treatment.
Identifiants
pubmed: 38793551
pii: v16050669
doi: 10.3390/v16050669
pii:
doi:
Substances chimiques
Peptides
0
HLA-A2 Antigen
0
HLA-A11 Antigen
0
HLA-A*02:01 antigen
0
HLA-A*11:01 antigen
0
Epitopes, T-Lymphocyte
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : National Key Research and Development Program of China Grant
ID : 2022YFC2305400