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Pneumococcal carriage and otitis media induce salivary antibodies to pneumococcal capsular polysaccharides in children.
J Infect Dis. 2002 Oct 15; 186(8):1106-14.JI

Abstract

Mucosal immunity likely plays an important role in the defense against Streptococcus pneumoniae. This study examined whether pneumococcal carriage and acute otitis media induce mucosal antibodies to pneumococcal capsular polysaccharides (Pnc-PSs) of types 1, 6B, 11A, 14, 19F, and 23F. Immunoglobulin (Ig) A, IgG, and secretory (S) Ig anti-Pnc-PS antibodies were measured by enzyme immunoassay in the saliva of children at ages 6, 12, 18, and 24 months and were analyzed in relation to the previous pneumococcal findings. A larger proportion of IgA-positive samples and higher concentrations of type-specific IgA antibodies were detected in samples of children with pneumococci of the given types cultured before sampling from nasopharyngeal samples or middle-ear fluid, compared with children who had cultures negative for pneumococci of the indicated types or of all types. The IgA and S-Ig concentrations correlated strongly, which suggests that the anti-Pnc-PS IgA was secretory. Salivary anti-Pnc-PS IgG was detected only rarely.

Authors+Show Affiliations

Department of Vaccines, National Public Health Institute, Mannerheimintie 166, 00300 Helsinki, Finland. birgit.simell@ktl.fiNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

12355361

Citation

Simell, Birgit, et al. "Pneumococcal Carriage and Otitis Media Induce Salivary Antibodies to Pneumococcal Capsular Polysaccharides in Children." The Journal of Infectious Diseases, vol. 186, no. 8, 2002, pp. 1106-14.
Simell B, Kilpi TM, Käyhty H. Pneumococcal carriage and otitis media induce salivary antibodies to pneumococcal capsular polysaccharides in children. J Infect Dis. 2002;186(8):1106-14.
Simell, B., Kilpi, T. M., & Käyhty, H. (2002). Pneumococcal carriage and otitis media induce salivary antibodies to pneumococcal capsular polysaccharides in children. The Journal of Infectious Diseases, 186(8), 1106-14.
Simell B, Kilpi TM, Käyhty H. Pneumococcal Carriage and Otitis Media Induce Salivary Antibodies to Pneumococcal Capsular Polysaccharides in Children. J Infect Dis. 2002 Oct 15;186(8):1106-14. PubMed PMID: 12355361.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Pneumococcal carriage and otitis media induce salivary antibodies to pneumococcal capsular polysaccharides in children. AU - Simell,Birgit, AU - Kilpi,Terhi M, AU - Käyhty,Helena, Y1 - 2002/09/16/ PY - 2002/04/02/received PY - 2002/06/14/revised PY - 2002/10/2/pubmed PY - 2002/11/26/medline PY - 2002/10/2/entrez SP - 1106 EP - 14 JF - The Journal of infectious diseases JO - J Infect Dis VL - 186 IS - 8 N2 - Mucosal immunity likely plays an important role in the defense against Streptococcus pneumoniae. This study examined whether pneumococcal carriage and acute otitis media induce mucosal antibodies to pneumococcal capsular polysaccharides (Pnc-PSs) of types 1, 6B, 11A, 14, 19F, and 23F. Immunoglobulin (Ig) A, IgG, and secretory (S) Ig anti-Pnc-PS antibodies were measured by enzyme immunoassay in the saliva of children at ages 6, 12, 18, and 24 months and were analyzed in relation to the previous pneumococcal findings. A larger proportion of IgA-positive samples and higher concentrations of type-specific IgA antibodies were detected in samples of children with pneumococci of the given types cultured before sampling from nasopharyngeal samples or middle-ear fluid, compared with children who had cultures negative for pneumococci of the indicated types or of all types. The IgA and S-Ig concentrations correlated strongly, which suggests that the anti-Pnc-PS IgA was secretory. Salivary anti-Pnc-PS IgG was detected only rarely. SN - 0022-1899 UR - https://www.unboundmedicine.com/medline/citation/12355361/Pneumococcal_carriage_and_otitis_media_induce_salivary_antibodies_to_pneumococcal_capsular_polysaccharides_in_children_ DB - PRIME DP - Unbound Medicine ER -