Identification of synthetic vaccine candidates against SARS CoV infection

Shu Pei Lien, Yi Ping Shih, Hsin Wei Chen, Jy Ping Tsai, Chih Hsiang Leng, Min Han Lin, Li Hsiu Lin, Hsin Yu Liu, Ai Hsiang Chou, Yu Wen Chang, Yi Ming A. Chen, Pele Chong, Shih Jen Liu

研究成果: 雜誌貢獻文章同行評審

12 引文 斯高帕斯(Scopus)


Three peptides, D1 (amino acid residues 175-201), D2 (a.a. 434-467), and TM (a.a. 1128-1159), corresponding to the spike protein (S) of severe acute respiratory syndrome corona virus (SARS CoV) were synthesized and their immunological functions were investigated in three different animals models (mice, guinea pigs, and rabbits). The peptides mixture formulated either with Freund's adjuvant or synthetic adjuvant Montanide ISA-51/oligodeoxy nucleotide CpG (ISA/CpG) could elicit antisera in immunized animals which were capable of inhibiting SARS/HIV pseudovirus entry into HepG2 cells. The neutralizing epitopes were identified using peptides to block the neutralizing effect of guinea pig antisera. The major neutralizing epitope was located on the D2 peptide, and the amino acid residue was fine mapped to 434-453. In BALB/c mice T-cell proliferation assay revealed that only D2 peptide contained T-cell epitope, the sequence of which corresponded to amino acid residue 434-448. The ISA/CpG formulation generated anti-D2 IgG titer comparable to those obtained from Freund's adjuvant formulation, but generated fewer antibodies against D1 or TM peptides. The highly immunogenic D2 peptide contains both neutralizing and Th cell epitopes. These results suggest that synthetic peptide D2 would be useful as a component of SARS vaccine candidates.
頁(從 - 到)716-721
期刊Biochemical and Biophysical Research Communications
出版狀態已發佈 - 7月 6 2007

ASJC Scopus subject areas

  • 生物物理學
  • 生物化學
  • 分子生物學
  • 細胞生物學


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