Serum antibodies to pneumococcal C polysaccharide in children
- 1 June 1987
- journal article
- research article
- Published by Wolters Kluwer Health in The Pediatric Infectious Disease Journal
- Vol. 6 (6), 519-526
- https://doi.org/10.1097/00006454-198706000-00006
Abstract
Immunoglobin class-specific antibody responses to the pneumococcal C polysaccharide (CPS) and to the capsular polysaccharides of type 3, 6A, 18C and 19F were measured by enzyme-linked immunosorbent assay in the sera of children ages 6 months to 7 years. Twenty of these children had acute otitis media caused by pneumococci of type/group 3, 6, 18 or 19, whereas 20 received an injection of 14-valent pneumococcal capsular polysaccharide vaccine. Many of the children in both groups had large concentrations of IgG and/or IgM class anti-CPS antibodies in their first serum sample. Both the infection and the vaccine elicited anti-CPS responses in all three immunoglobulin classes, most notably IgG. The pneumococcal capsular polysaccharides used as antigens in the enzyme linked immunosorbent assay were found to contain CPS in amounts ranging from < 1 to 30%. As a result the enzyme-linked immunosorbent assay detected both anti-type-specific and anti-CPS antibodies. After elimination of the anti-CPS, type-specific pneumococcal antibodies were found only occasionally and in low concentrations in serum samples obtained in the acute phase of otitis or before vaccination. The infection induced homologous type-specific pneumococcal antibodies to varying degrees depending on the type: regularly to type 3; and fairly regularly to type 18C polysaccharide, but seldom to type 6 or 19. The pneumococcal vaccine induced type-specific antibodies to all four types measured, but the response to type 6A was poor.This publication has 2 references indexed in Scilit:
- Determination of antibodies to pneumococcal C polysaccharide in patients with community-acquired pneumoniaJournal of Clinical Microbiology, 1985
- Polyvalent Pneumococcal-Polysaccharide Immunization of Patients with Sickle-Cell Anemia and Patients with SplenectomyNew England Journal of Medicine, 1977