Glycoconjugation process
The present disclosure relates generally to methods of preparing glycoconjugates containing a saccharide conjugated to a carrier protein by use of stable nitroxyl radical related agent/oxidant as an oxidizing agent, to immunogenic compositions comprising such glycoconjugates, and to methods for the use of such glycoconjugates and immunogenic compositions.
1. An immunogenic composition comprising a glycoconjugate comprising a S. pneumoniae serotype 12F capsular polysaccharide conjugated via an oxidized primary hydroxyl group to a carrier protein, wherein the oxidized primary hydroxyl group is present on an α-D-Glop or a 2-Glcp sugar residue of said S. pneumoniae serotype 12F capsular polysaccharide, wherein said glycoconjugate has a molecular weight of between about 500 kDa and about 5,000 kDa and a saccharide:carrier protein ratio (w/w) between 0.2 and 4, wherein the amount of free S. pneumoniae serotype 12F polysaccharide in the composition is less than about 35% free saccharide relative to total S. pneumoniae serotype 12F polysaccharide.
2. The immunogenic composition of claim 1 , wherein said S. pneumoniae serotype 12F capsular polysaccharide has a molecular weight of between about 50 kDa and about 500 kDa.
3. The immunogenic composition of claim 1 , wherein said S. pneumoniae serotype 12F capsular polysaccharide has a molecular weight of between about 90 kDa and about 250 kDa.
4. The immunogenic composition of claim 1 , wherein said saccharide:carrier protein ratio (w/w) is between 0.9 and 1.7.
5. The immunogenic composition of claim 1 , wherein said saccharide:carrier protein ratio (w/w) is between 1.1 and 1.7.
6. The immunogenic composition of claim 1 , wherein said glycoconjugate has a molecular weight of between about 1000 kDa and about 3600 kDa.
7. The immunogenic composition of claim 1 , wherein said glycoconjugate has a molecular weight of between about 1000 kDa and about 3000 kDa.
8. The immunogenic composition of claim 1 , wherein the amount of free S. pneumoniae serotype 12F polysaccharide in the composition is less than 35% when maintained at 25° C. for 120 days from when it was prepared.
9. The immunogenic composition of claim 1 , wherein the amount of free S. pneumoniae serotype 12F polysaccharide in the composition is less than 30% when maintained at 25° C. for 120 days from when it was prepared.
10. The immunogenic composition of claim 1 , wherein the amount of free S. pneumoniae serotype 12F polysaccharide in the composition is less than 25% when maintained at 25° C. for 120 days from when it was prepared.
11. The immunogenic composition of claim 1 , wherein said carrier protein is a toxoid.
12. The immunogenic composition of claim 1 , wherein said carrier protein is a toxin from tetanus, diphtheria, pertussis, Pseudomonas, E. coli, Staphylococcus or Streptococcus.
13. The immunogenic composition of claim 1 , wherein said carrier protein is CRM 197 .
14. The immunogenic composition of claim 1 , further comprising a pharmaceutically acceptable excipient, carrier, or diluent.
15. The immunogenic composition of claim 1 , further comprising an additional antigen.
16. The immunogenic composition of claim 15 , wherein the additional antigen comprises a protein antigen or a glycoconjugate of a capsular polysaccharide derived from S. pneumoniae.
17. The immunogenic composition of claim 16 , wherein the additional antigen comprises a glycoconjugate of a capsular polysaccharide selected from S. pneumoniae serotypes 1, 4, 5, 6A, 6B, 7F, 8, 9V, 11A, 14, 15B, 18C, 19A, 19F, 22F, and 23F capsular polysaccharides.
18. The immunogenic composition of claim 1 , further comprising a glycoconjugate of a capsular polysaccharide from a S. pneumoniae serotype selected from the group of serotypes consisting of 1, 3, 4, 5, 6A, 6B, 7F, 8, 9V, 10A, 11A, 14, 15B, 18C, 19A, 19F, 22F, 23F, and 33F.
19. The immunogenic composition of claim 1 , further comprising an adjuvant.
20. The immunogenic composition of claim 19 , wherein the adjuvant is an aluminum-based adjuvant selected from aluminum phosphate, aluminum sulfate, and aluminum hydroxide.
21. The immunogenic composition of claim 18 , further comprising glycoconjugates of capsular polysaccharide from S. pneumoniae serotypes 1, 3, 4, 5, 6A, 6B, 7F, 8, 9V, 10A, 11A, 14, 15B, 18C, 19A, 19F, 22F, 23F, and 33F.
22. An immunogenic composition comprising a glycoconjugate comprising a S. pneumoniae serotype 12F capsular polysaccharide conjugated via an oxidized primary hydroxyl group on an α-D-Glcp or a 2-Glcp sugar residue to a carrier protein.
23. The immunogenic composition of claim 22 , wherein said carrier protein is CRM 197 .
24. The immunogenic composition of claim 23 , wherein the amount of free S. pneumoniae serotype 12F polysaccharide in the composition is less than about 35% free saccharide relative to total S. pneumoniae serotype 12F polysaccharide.
25. The immunogenic composition of claim 24 , wherein the amount of free S. pneumoniae serotype 12F polysaccharide in the composition is less than 35% when maintained at 25° C. for 120 days from when it was prepared.