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Homogeneous Glycoconjugate Produced by Combined Unnatural Amino Acid Incorporation and Click-Chemistry for Vaccine Purposes
Published on: December 19, 2020
Novel polysaccharide-protein conjugates provide an immunogenic 13-valent pneumococcal conjugate vaccine for
Allison E B Turner1,2, Jonas E Gerson1,2, Helen Y So2
1Vaccine Research and Development, PnuVax Incorporated Headquarters, 134 Albert St., Kingston, Ontario, K7L 3V2, Canada.
Insights
Developing new pneumococcal conjugate vaccines (PCVs) is crucial for global child health. This study presents novel, high-yield PCV-13 conjugates that are immunogenic in animal models, offering a promising alternative to existing vaccines.
Area of Science:
- Vaccinology
- Microbiology
- Immunology
Background:
- Pneumonia is the leading cause of childhood mortality globally.
- Existing pneumococcal conjugate vaccines (PCVs) face challenges in cost and supply, limiting access in developing regions.
- There is a need for accessible and effective PCVs for global child health.
Purpose of the Study:
- To develop and characterize novel high-yield pneumococcal conjugate vaccines (PCVs).
- To assess the immunogenicity of a new 13-valent PCV (PCV-13) in animal models.
- To compare the novel PCV-13 with a commercially available vaccine, Prevnar®13.
Main Methods:
- Production and purification of pneumococcal polysaccharides (PnPSs) and CRM197 carrier protein.
- Conjugation of PnPSs to CRM197 using cyanide-free, in vacuo glycation methods.
- In vitro characterization of conjugates and in vivo immunogenicity studies in animals, including dose-response and comparative analyses.
Main Results:
- Successful generation of high molecular weight PnPS-CRM conjugates with low free protein.
- Demonstrated boostability of all 13 serotypes in the novel PCV-13 after a second dose.
- Immunogenicity results showed that 10 out of 13 serotypes in the novel PCV-13 were statistically similar or superior to Prevnar®13.
Conclusions:
- The novel polysaccharide-protein conjugates are highly promising for human PCV development.
- The in vacuo conjugation technique is versatile and adaptable for developing other conjugate vaccines.
- This work contributes to the development of more accessible and effective PCVs for global child health.
Abstract:
Pneumonia remains the single leading cause of childhood death worldwide. Despite the commercial availability of multiple pneumococcal conjugate vaccines (PCVs), high dosage cost and supply shortages prevent PCV delivery to much of the developing world. The current work presents high-yield pneumococcal conjugates that are immunogenic in animals and suitable for use in human vaccine development. The 13-valent pneumococcal conjugate vaccine (PCV-13) investigated in this research incorporated serotypes 1, 3, 4, 5, 6A, 6B, 7F, 9V, 14, 18C, 19A, 19F, and 23F. Pneumococcal polysaccharides (PnPSs) and CRM197 carrier protein were produced and purified in-house, and used to prepare PnPS-CRM conjugates using unique, cyanide-free, in vacuo glycation conjugation methods. In vitro characterization confirmed the generation of higher molecular weight PnPS-CRM conjugates low in free protein. In vivo animal studies were performed to compare PnuVax's PCV-13 to the commercially available PCV-13, Prevnar®13 (Pfizer, USA). A boost dose was provided to all groups post-dose 1 at t = 14 days. Post-dose 2 results at t = 28 days showed that all 13 serotypes in PnuVax's PCV-13 were boostable. Per serotype IgG GMCs demonstrated that PnuVax's PCV-13 is immunogenic for all 13 serotypes, with 10 of the 13 serotypes statistically the same or higher than Prevnar®13 post-dose 2. As a result, the novel polysaccharide-protein conjugates developed in this work are highly promising for use in human PCV development. The in vacuo conjugation technique applied in this work could also be readily adapted to develop many other conjugate vaccines.
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