Franzoni Giulia, Kurkure Nitin V, Essler Sabine E, Pedrera Miriam, Everett Helen E, Bodman-Smith Kikki B, Crooke Helen R, Graham Simon P
Virology Department, Animal Health and Veterinary Laboratories Agency, Addlestone, United Kingdom ; Department of Microbial & Cellular Sciences, University of Surrey, Guildford, United Kingdom.
Virology Department, Animal Health and Veterinary Laboratories Agency, Addlestone, United Kingdom ; Nagpur Veterinary College, Maharashtra Animal & Fishery Sciences University, Nagpur, India.
PLoS One. 2013 Dec 23;8(12):e84246. doi: 10.1371/journal.pone.0084246. eCollection 2013.
Vaccination with live attenuated classical swine fever virus (CSFV) vaccines induces a rapid onset of protection which has been associated with virus-specific CD8 T cell IFN-γ responses. In this study, we assessed the specificity of this response, by screening a peptide library spanning the CSFV C-strain vaccine polyprotein to identify and characterise CD8 T cell epitopes. Synthetic peptides were pooled to represent each of the 12 CSFV proteins and used to stimulate PBMC from four pigs rendered immune to CSFV by C-strain vaccination and subsequently challenged with the virulent Brescia strain. Significant IFN-γ expression by CD8 T cells, assessed by flow cytometry, was induced by peptide pools representing the core, E2, NS2, NS3 and NS5A proteins. Dissection of these antigenic peptide pools indicated that, in each instance, a single discrete antigenic peptide or pair of overlapping peptides was responsible for the IFN-γ induction. Screening and titration of antigenic peptides or truncated derivatives identified the following antigenic regions: core₂₄₁₋₂₅₅ PESRKKLEKALLAWA and NS3₁₉₀₂₋₁₉₁₂ VEYSFIFLDEY, or minimal length antigenic peptides: E2₉₉₆₋₁₀₀₃ YEPRDSYF, NS2₁₂₂₃₋₁₂₃₀ STVTGIFL and NS5A₃₀₇₀₋₃₀₇₈ RVDNALLKF. The epitopes are highly conserved across CSFV strains and variable sequence divergence was observed with related pestiviruses. Characterisation of epitope-specific CD8 T cells revealed evidence of cytotoxicity, as determined by CD107a mobilisation, and a significant proportion expressed TNF-α in addition to IFN-γ. Finally, the variability in the antigen-specificity of these immunodominant CD8 T cell responses was confirmed to be associated with expression of distinct MHC class I haplotypes. Moreover, recognition of NS₁₂₂₃₋₁₂₃₀ STVTGIFL and NS3₁₉₀₂₋₁₉₁₂ VEYSFIFLDEY by a larger group of C-strain vaccinated animals showed that these peptides could be restricted by additional haplotypes. Thus the antigenic regions and epitopes identified represent attractive targets for evaluation of their vaccine potential against CSFV.
用减毒活经典猪瘟病毒(CSFV)疫苗进行接种可迅速产生保护作用,这与病毒特异性CD8 T细胞的IFN-γ反应有关。在本研究中,我们通过筛选覆盖CSFV C株疫苗多聚蛋白的肽库来评估这种反应的特异性,以鉴定和表征CD8 T细胞表位。合成肽被汇集起来以代表12种CSFV蛋白中的每一种,并用于刺激来自4头经C株疫苗接种而对CSFV产生免疫、随后用强毒布雷西亚株攻击的猪的外周血单核细胞(PBMC)。通过流式细胞术评估,代表核心蛋白、E2蛋白、NS2蛋白、NS3蛋白和NS5A蛋白的肽库诱导了CD8 T细胞显著的IFN-γ表达水平。对这些抗原肽库的剖析表明,在每种情况下,单个离散的抗原肽或一对重叠肽负责IFN-γ的诱导。对抗原肽或截短衍生物的筛选和滴定确定了以下抗原区域:核心蛋白₂₄₁₋₂₅₅ PESRKKLEKALLAWA和NS3₁₉₀₂₋₁₉₁₂ VEYSFIFLDEY,或最小长度的抗原肽:E2₉₉₆₋₁₀₀₃ YEPRDSYF、NS2₁₂₂₃₋₁₂₃₀ STVTGIFL和NS5A₃₀₇₀₋₃₀₇₈ RVDNALLKF。这些表位在CSFV各毒株间高度保守,而与相关瘟病毒相比则观察到可变的序列差异。表位特异性CD8 T细胞的表征揭示了细胞毒性的证据,这通过CD107a的动员来确定,并且很大一部分细胞除了表达IFN-γ外还表达TNF-α。最后,证实这些免疫显性CD8 T细胞反应的抗原特异性变异性与不同的MHC I类单倍型的表达有关。此外,更大组的经C株疫苗接种的动物对NS₁₂₂₃₋₁₂₃₀ STVTGIFL和NS3₁₉₀₂₋₁₉₁₂ VEYSFIFLDEY的识别表明这些肽可能受其他单倍型的限制。因此,鉴定出的抗原区域和表位是评估其抗CSFV疫苗潜力的有吸引力的靶点。