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Generation of plant-derived recombinant DTP subunit vaccine
R Brodzik1, S Spitsin, N Pogrebnyak
1Biotechnology Foundation Laboratories at Thomas Jefferson University, 1020 Locust Street, Philadelphia, PA 19107, USA.
Insights
Researchers developed a plant-based subunit diphtheria-tetanus-pertussis (DTP) vaccine using recombinant technology. This approach offers a potentially safer, more cost-effective, and renewable alternative to traditional DTP vaccines.
Area of Science:
- Biotechnology
- Vaccinology
- Molecular Biology
Background:
- Current diphtheria-tetanus-pertussis (DTP) vaccines are produced from pathogenic bacteria, posing risks of adverse effects and complex, costly manufacturing.
- The standard US vaccination schedule requires five doses of the acellular DTaP vaccine for children.
Purpose of the Study:
- To develop a safer, more easily renewable, and less expensive subunit DPT vaccine using recombinant technology.
- To explore the feasibility of producing vaccine components in non-pathogenic plant expression systems.
Main Methods:
- Utilized recombinant technology to express diphtheria toxin (DT), tetanus fragment-C (TetC), and pertussis toxin S1 (PTX S1) antigenic proteins in tobacco plants and carrot cell cultures.
- Purified the expressed proteins to levels suitable for intramuscular injection.
- Administered the purified proteins to BALB/c mice to assess immunogenicity.
Main Results:
- Successfully expressed soluble forms of DT, TetC, and PTX S1 antigenic proteins in plant systems.
- Achieved efficient downstream purification of these proteins.
- Demonstrated that 5µg per dose of the plant-derived vaccine components induced high levels of antigen-specific IgGs in mouse sera.
Conclusions:
- The study supports the feasibility of producing recombinant pediatric vaccine components, specifically for DTP, in plant-based expression systems.
- Plant-derived vaccine components show promise as a safer and more sustainable alternative to conventional vaccines.
Abstract:
The current diphtheria-tetanus-pertussis (DTP) pediatric vaccine is produced from the corresponding pathogenic bacteria Corynebacterium diphtheriae, Clostridium tetani and Bordetella pertussis; five injected doses of DTaP (acellular) vaccine are required for every child in the standard US vaccination schedule. Because the vaccine is derived from native live sources, adverse effects are possible and production is complex and costly. To address issues of safety, ease of renewability and expense, we used recombinant technology in an effort to develop a subunit DPT vaccine derived in non-pathogenic plant expression systems. Expression of diphtheria toxin (DT), tetanus fragment-C (TetC) and the non-toxic S1 subunit of pertussis toxin (PTX S1) antigenic proteins in soluble form in low-alkaloid tobacco plants and carrot cell cultures allowed efficient downstream purification to levels suitable for intramuscular injection in BALB/c mice. At working concentrations of 5mug per dose, these preparations induced high levels of antigen-specific IgGs in mouse sera. Our results clearly support the feasibility of producing recombinant pediatric vaccine components in plants.
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