Key result
A novel T-cell epitope located on the FMDV structural protein 1D (VP1, amino acids 66-80) induced proliferation and interferon-gamma production in all investigated cattle with MHC serotype A31.
The study identifies a novel immunodominant T-cell epitope on the FMDV structural protein 1D (VP1) in cattle with MHC serotype A31, which may inform future vaccine design.
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May guide FMDV T-cell vaccine design in A31 cattle; leaves open validation across MHC types and species.
To identify foot-and-mouth disease virus (FMDV) specific T-cell epitopes within the entire polyprotein sequence of the virus, 442 overlapping pentadecapeptides were tested in proliferation assays using lymphocytes from cattle experimentally infected with FMDV. Four months post-infection cells from all investigated animals (n = 4) responded by proliferation and interferon-gamma production to a peptide located on the structural protein 1D (VP1), amino acid residues 66-80. Major histocompatibility complex (MHC) serotyping of the investigated cattle indicated that all animals shared the MHC serotype A31 which comprises the class II allele DRB3 0701. This may explain the common recognition of this newly discovered epitope. Responses to other peptides could only be observed in one animal and rapidly declined during the time course of the study. These observations point to an immunodominant role of this epitope located on the protein 1D in cattle with MHC serotype A31.
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Gerner et al. (2007) studied Foot-and-mouth disease virus (FMDV) infection (n=4). FMDV overlapping pentadecapeptides vs. Control peptide and medium alone was evaluated on T-cell proliferation and IFN-γ production. A novel T-cell epitope located on the FMDV structural protein 1D (VP1, amino acids 66-80) induced proliferation and interferon-gamma production in all investigated cattle with MHC serotype A31.
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