Selected article for: "IgG antibody and SARS spike protein"

Author: Zhao, Ping; Ke, Jin-Shan; Qin, Zhao-Lin; Ren, Hao; Zhao, Lan-Juan; Yu, Jian-Guo; Gao, Jun; Zhu, Shi-Ying; Qi, Zhong-Tian
Title: DNA Vaccine of SARS-Cov S Gene Induces Antibody Response in Mice
  • Cord-id: 65iwx5nv
  • Document date: 2004_1_25
  • ID: 65iwx5nv
    Snippet: The spike (S) protein, a main surface antigen of SARS-coronavirus (SARS-CoV), is one of the most important antigen candidates for vaccine design. In the present study, three fragments of the truncated S protein were expressed in E. coli, and analyzed with pooled sera of convalescence phase of SARS patients. The full length S gene DNA vaccine was constructed and used to immunize BALB/c mice. The mouse serum IgG antibody against SARS-CoV was measured by ELISA with E. coli expressed truncated S pro
    Document: The spike (S) protein, a main surface antigen of SARS-coronavirus (SARS-CoV), is one of the most important antigen candidates for vaccine design. In the present study, three fragments of the truncated S protein were expressed in E. coli, and analyzed with pooled sera of convalescence phase of SARS patients. The full length S gene DNA vaccine was constructed and used to immunize BALB/c mice. The mouse serum IgG antibody against SARS-CoV was measured by ELISA with E. coli expressed truncated S protein or SARS-CoV lysate as diagnostic antigen. The results showed that all the three fragments of S protein expressed by E. coli was able to react with sera of SARS patients and the S gene DNA candidate vaccine could induce the production of specific IgG antibody against SARS-CoV efficiently in mice with seroconversion ratio of 75% after 3 times of immunization. These findings lay some foundations for further understanding the immunology of SARS-CoV and developing SARS vaccines.

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