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Vaccine Detail
Herpes simplex virus type 1 DNA vaccine encoding GD |
Vaccine Information |
- Vaccine Name: Herpes simplex virus type 1 DNA vaccine encoding GD
- Target Pathogen: Herpes simplex virus type 1 and 2
- Target Disease: Herpes
- Vaccine Ontology ID: VO_0011421
- Type: DNA vaccine
- Status: Research
- Antigen: Herpes simplex virus type1 glycoprotein D
- US5
gene engineering:
- Type: DNA vaccine construction
- Description: Plasmid DNA encoding HSV-1 glycoprotein D1 (gD1) was constructed by insertion of the gD1 gene into pcDNA3 (Jamali et al., 2009).
- Detailed Gene Information: Click Here.
- DNA vaccine plasmid:
- DNA vaccine plasmid name:
- DNA vaccine plasmid VO ID: VO_0000132
- Immunization Route: Intradermal injection (i.d.)
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Host Response |
Mouse Response
- Host Strain: BALB/c
- Vaccination Protocol: BALB/c mice were immunized three times intra-dermally with 50 µg of pcDNA3 gD1 in a total volume of 100 µl on days 0, 21 and 42 (gD1 group). NLX (Sigma) was dissolved in 100 µl PBS containing 50 µg of the pcDNA3 gD1 construct at a concentration of 5 mg kg–1 and injected to each mouse with the same protocol, i.e. NLX was administered intra-dermally in combination with the pcDNA3 gD1 on days 0, 21 and 42 (NLX-gD1 group). PBS was injected according to the same protocol into the third group of mice as a negative control (PBS group). Finally, the last control group of mice was inoculated according to the same protocol with 100 µl of inoculums containing 10^5 plaque-forming units (pfu) of KOS strain virus (KOS group) (Jamali et al., 2009).
- Challenge Protocol: Three weeks after the last immunization, mice were challenged with a low dose [four mouse lethal dose fifty percent (MLD50) = 1 x 10^5 pfu] or a high dose (10 MLD50 = 1 x 10^5 pfu) of wild-type virus. The mortality rate was followed for 2 weeks (Jamali et al., 2009).
- Efficacy: BALB/c mice receiving a glycoprotein D1 (gD1, US5) DNA vaccine alone were 80% protected against a subsequent HSV-1 challenge. Results also indicate that the administration of NLX as an adjuvant improved protective immunity against HSV-1 (Jamali et al., 2009).
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References |
Jamali et al., 2009: Jamali A, Mahdavi M, Hassan ZM, Sabahi F, Farsani MJ, Bamdad T, Soleimanjahi H, Motazakker M, Shahabi S. A novel adjuvant, the general opioid antagonist naloxone, elicits a robust cellular immune response for a DNA vaccine. International immunology. 2009; 21(3); 217-225. [PubMed: 19174474].
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