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Revealing novel and conservative CD8+T-cell epitopes with MHC B2 restriction on ALV-J.
- Source :
- Veterinary Research; 12/18/2024, Vol. 55 Issue 1, p1-10, 10p
- Publication Year :
- 2024
-
Abstract
- MHC B2 haplotype chickens have been reported to induce strong immune response against various avian pathogens. However, little is known about the CD8<superscript>+</superscript>T-cell epitope with MHC B2-restricted on subgroup J avian leukosis virus (ALV-J). In this study, we explored the ALV-J-induced cellular immune response in B2 haplotype chickens in vivo. We found that ALV-J infection significantly increased the proportion of CD8<superscript>+</superscript>T cells in chickens and up-regulated the expression of cytotoxic genes like Granzyme A and antiviral genes like IFIT5 at 14 days post-infection (dpi). We selected 32 candidate peptides based on the peptide-binding motif and further identified three MHC B2-restricted CD8<superscript>+</superscript>T epitopes on ALV-J, including Pol<subscript>652−660</subscript>, Gag<subscript>374−382,</subscript> and Gag<subscript>403−411</subscript> which induced significant levels of chicken IFN-γ production in splenocytes from ALV-J infected chickens using the ELISpot assay. In addition, we also verified that the three identified epitopes stimulated memory splenocytes elevating TNF-α and IL-2 protein expression. Importantly, we found that the three positive peptides were highly conserved among ALV-A, ALV-B, ALV-E, ALV-J, and ALV-K. Taken together, we identified three MHC B2-restricted CD8<superscript>+</superscript>T cell epitopes on ALV-J, providing a foundation for developing effective T cell epitope vaccines targeting conserved internal viral proteins. [ABSTRACT FROM AUTHOR]
- Subjects :
- AVIAN leukosis
VIRAL proteins
HAPLOTYPES
MEDICAL sciences
PROTEIN expression
Subjects
Details
- Language :
- English
- ISSN :
- 09284249
- Volume :
- 55
- Issue :
- 1
- Database :
- Complementary Index
- Journal :
- Veterinary Research
- Publication Type :
- Academic Journal
- Accession number :
- 181780606
- Full Text :
- https://doi.org/10.1186/s13567-024-01426-3