Comparative Immunogenicity of Group 6 Pneumococcal Type 6A(6) and Type 6B(26) Capsular Polysaccharides
- 1 December 1979
- journal article
- research article
- Published by American Society for Microbiology in Infection and Immunity
- Vol. 26 (3) , 1116-1122
- https://doi.org/10.1128/iai.26.3.1116-1122.1979
Abstract
The comparative immunogenicity of the two cross-reacting group 6 pneumococcal capsular polysaccharides, type 6A(6) and type 6B(26), was studied with hyperimmune rabbit typing antisera and with sera from adult volunteers injected with polyvalent pneumococcal vaccines containing either 50 μg of type 6A (U.S. designation, type 6) or 50 μg each of type 6A and type 6B (U.S. designation, type 26) polysaccharides. Both group 6 polysaccharides were linear copolymers composed of 1 mol each of d-galactose, d-glucose, l-rhamnose, and d-ribitol phosphate. They differed only in that type 6A had a rhammopyranosyl-(1 → 3)-d-ribitol bond and the type 6B had a rhamnopyranosyl-(1 → 4)-d-ribitol bond. Quantitative precipitation and absorption analyses with rabbit hyperimmune antisera induced by simultaneous injection with type 6A and type 6B organisms revealed extensive cross-reactions between the two group 6 polysaccharides. There was less, although still quite extensive, cross-reactivity between the two group 6 polysaccharides examined with antisera from rabbits injected with only one of the group 6 pneumococci. In a radioimmunoassay, using 14C internally labeled type 6A or type 6B polysaccharide antigens, there was no difference in the serum antibody level to either type of volunteer injected with polyvalent pneumococcal vaccines containing type 6A or both type 6A and type 6B polysaccharides. These studies indicate that the structural similarity of the pneumococcal group 6 polysaccharides confers extensive cross-reactivity with hyperimmune typing antisera prepared with whole organisms or after injection of purified polysaccharides in adult volunteers. With our current polysaccharides, it appears that a polyvalent pneumococcal vaccine formulation that contains only type 6A will serve to induce the maximum amount of serum antibodies to both group 6 organisms. ImagesThis publication has 21 references indexed in Scilit:
- Structural studies of the capsular antigen from streptococcus pneumoniae type 26Carbohydrate Research, 1979
- Failure of Pneumococcal Vaccine in Children with Sickle-Cell DiseaseNew England Journal of Medicine, 1979
- Death from Type 6 Pneumococcal Septicemia in a Vaccinated Child with Sickle-Cell DiseaseNew England Journal of Medicine, 1979
- PNEUMOCOCCAL INFECTION AFTER VACCINATIONThe Lancet, 1978
- Impaired Response to Pneumococcal Vaccine in Hodgkin's DiseaseNew England Journal of Medicine, 1978
- Impaired Antibody Response to Pneumococcal Vaccine after Treatment for Hodgkin's DiseaseNew England Journal of Medicine, 1978
- Structural studies on the sialic acid polysaccharide antigen of Escherichia coli strain Bos-12Biochemistry, 1977
- Standardization and control of meningococcal vaccines, group A and group C polysaccharidesJournal of Biological Standardization, 1977
- Clinical evaluation of group A and group C meningococcal polysaccharide vaccines in infants.Journal of Clinical Investigation, 1975
- HUMAN IMMUNITY TO THE MENINGOCOCCUSThe Journal of Experimental Medicine, 1969