Identification of T-cell epitopes in the structural and non-structural proteins of classical swine fever virus

被引:65
作者
Armengol, E
Wiesmüller, KH
Wienhold, D
Büttner, M
Pfaff, E
Jung, G
Saalmüller, A
机构
[1] Fed Res Ctr Virus Dis Anim, Inst Immunol, D-72076 Tubingen, Germany
[2] EMC Microcollect GmbH, D-72070 Tubingen, Germany
[3] Univ Tubingen, Inst Organ Chem, D-72076 Tubingen, Germany
关键词
D O I
10.1099/0022-1317-83-3-551
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
To identify new T-cell epitopes of classical swine fever virus (CSFV), 573 overlapping, synthetic pentadecapeptides spanning 82% of the CSFV (strain Glentorf) genome sequence were synthesized and screened. In proliferation assays, 26 peptides distributed throughout the CSFV viral protein sequences were able to induce specific T-cell responses in PBMCs from a CSFV-Glentorf-infected d/d haplotype pig. Of these 26 peptides, 18 were also recognized by PBMCs from a CSFV-Alfort/187-infected d/d haplotype pig. In further experiments, it could be shown that peptide 290 (KHKVRNEVMVHWFDD), which corresponds to amino acid residues 1446-1460 of the CSFV non-structural protein NS2-3 could induce interferon-gamma secretion after secondary in vitro restimulation. The major histocompatibility complex (MHC) restriction for stimulation of T-cells by this pentadecapeptide was identified as being mainly MHC class II and partially MHC class I. In cytolytic assays, CSFV-specific cytotoxic T-lymphocytes (CTLs) were able to lyse peptide 290-loaded target cells. These findings indicate the existence of a CSFV-specific helper T-cell epitope and a CTL epitope in this peptide.
引用
收藏
页码:551 / 560
页数:10
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