Nasopharyngeal antibodies to pneumococcal pneumolysin in children with acute otitis media

Pneumolysin, an intracellular protein toxin of all clinically relevant pneumococcal serotypes, is released in vivo during the autolysis of pneumococci and is believed to pave the way for intact pneumococci to invade and cause disease. Therefore, antibodies to pneumolysin should prevent its destructive function. We measured antibodies to pneumococcal pneumolysin in acute- and convalescent-phase nasopharyngeal aspirate samples of 120 children (median age, 2.5 years) with acute otitis media by enzyme immunoassay. Nasopharyngeal immunoglobulin M (IgM) and IgG class antibodies to pneumolysin were rarely detectable, whereas IgA class antibody was detected often, occurred independently of serum IgA antibody in serum, and correlated with the presence of the secretory component in pneumococcal antibody, indicating local production of IgA antibodies. Nasopharyngeal IgA antibody to pneumolysin was detected in 93% of the children already in the acute phase of otitis. Twenty percent of the children developed at least a threefold rise in the pneumolysin-specific IgA antibody concentration by the convalescent phase of otitis, with the youngest at 6 months of age, regardless of the pneumococcal findings in the nasopharynx or middle ear fluid. We suggest that nasopharyngeal IgA antibody to pneumolysin can be produced early in life by pneumococcal colonization.

[1]  M. Leinonen,et al.  Nasopharyngeal antibodies to pneumococcal capsular polysaccharides in children with acute otitis media. , 1995, The Journal of infectious diseases.

[2]  M. Leinonen,et al.  Diagnosis of bacteremic pneumococcal pneumonia by amplification of pneumolysin gene fragment in serum. , 1995, The Journal of infectious diseases.

[3]  M. Leinonen,et al.  Comparison of PCR assay with bacterial culture for detecting Streptococcus pneumoniae in middle ear fluid of children with acute otitis media , 1994, Journal of clinical microbiology.

[4]  M. Leinonen,et al.  Mapping of immunoreactive sites of pneumococcal pneumolysin by use of synthetic peptides , 1993, Infection and immunity.

[5]  J C Paton,et al.  Molecular analysis of the pathogenicity of Streptococcus pneumoniae: the role of pneumococcal proteins. , 1993, Annual review of microbiology.

[6]  C. Bluestone,et al.  Ten‐year review of otitis media pathogens , 1992, The Pediatric infectious disease journal.

[7]  C. Svanborg,et al.  Nasopharyngeal colonization during the first year of life. , 1992, The Journal of infectious diseases.

[8]  G. Boulnois,et al.  Structure and function of pneumolysin, the multifunctional, thiol‐activated toxin of Streptococcus pneumoniae , 1991, Molecular microbiology.

[9]  P. Andrew,et al.  Complement activation and antibody binding by pneumolysin via a region of the toxin homologous to a human acute‐phase protein , 1991, Molecular microbiology.

[10]  Henry D. Isenberg,et al.  Manual of Clinical Microbiology , 1991 .

[11]  J. Bernstein,et al.  Changes in nasopharyngeal flora during otitis media of childhood , 1990, The Pediatric infectious disease journal.

[12]  M. Sarvas,et al.  Production of pneumolysin, a pneumococcal toxin, in Bacillus subtilis. , 1989, Gene.

[13]  H. Sørensen Management of postoperative laryngeal edema following laryngoscopy for procedures as simple as biopsy of a tumor. , 1987 .

[14]  O. Ruuskanen,et al.  Finnish Approach to the Treatment of Acute Otitis Media Report of the Finnish Consensus Conference , 1987, The Annals of otology, rhinology & laryngology. Supplement.

[15]  R. Möllby,et al.  Production and purification of Streptococcus pneumoniae hemolysin (pneumolysin) , 1987, Journal of clinical microbiology.

[16]  H. Sørensen Finnish approach to the treatment of acute otitis media. , 1987, The Annals of otology, rhinology, and laryngology.

[17]  J. Paton,et al.  Effect of immunization with pneumolysin on survival time of mice challenged with Streptococcus pneumoniae , 1983, Infection and immunity.

[18]  M. Pichichero,et al.  A mucosal antibody response following systemic Haemophilus influenzae type B infection in children. , 1981, The Journal of clinical investigation.

[19]  J. Alroy,et al.  Localization of C-reactive protein in inflammatory lesions of experimental allergic encephalomyelitis. , 1981, Clinical and experimental immunology.

[20]  S. Alaluusua,et al.  Quantitation of IgA in Human Whole Saliva , 1981 .

[21]  B. Gray,et al.  Epidemiologic studies of Streptococcus pneumoniae in infants: acquisition, carriage, and infection during the first 24 months of life. , 1980, The Journal of infectious diseases.

[22]  J. Bienenstock,et al.  Evidence for a common mucosal immunologic system. I. Migration of B immunoblasts into intestinal, respiratory, and genital tissues. , 1979, Journal of immunology.

[23]  M. Johnson Cellular location of pneumolysin , 1977 .

[24]  Ellen Jo Baron,et al.  Manual of clinical microbiology , 1975 .