Abstract
Immunization of mice with Fragment C protein, the non-toxic C-terminal domain of tetanus toxin, will protect mice against lethal challenge with tetanus toxin. A plasmid, pcDNA3/tetC, which encodes a synthetic tetC gene expressed under the control of the human cytomegalovirus major intermediate early promoter/enhancer region, was constructed. Fragment C expression was observed in Chinese hamster ovary cells following transfection with pcDNA3/tetC. The immune response induced by intramuscular immunization with pure pcDNA3/tetC DNA was evaluated in a murine model. Anti-Fragment C serum immunoglobulin and proliferative responses in splenocytes were observed following two immunizations with pcDNA3/tetC. The major IgG subclass that recognized Fragment C was IgG2a and the stimulated splenocytes secreted high levels of interferon-γ. Sufficient anti-Fragment C serum immunoglobulins were induced by DNA-mediated Immunization to protect mice against lethal challenge with tetanus toxin.
| Original language | English |
|---|---|
| Pages (from-to) | 827-829 |
| Number of pages | 3 |
| Journal | Vaccine |
| Volume | 15 |
| Issue number | 8 |
| DOIs | |
| Publication status | Published - 1 Jun 1997 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Fragment C protein
- Immunization
- Tetanus toxin
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