1984
DOI: 10.1016/s0165-5876(84)80052-x
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Pneumococcal antibodies and complement during and after periods of recurrent otitis

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Cited by 69 publications
(35 citation statements)
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“…Children with ROM or persistent OME have been shown also to exhibit insufficient antibody responses to pneumococcal polysaccharides of type 6A and 19F [4], P6 protein of NTHi [5,6], and CD protein of M. catarrhalis [8], and the poor response to these antigens has been attributed to their weak immunogenicity [26]. The anti-LTA antibody level showed only one hundredth fold levels of anti-whole cell body antibody, which concurred with results shown elsewhere [27,28], suggesting that the immunogenicity of LTA may be weak.…”
Section: Discussionmentioning
confidence: 99%
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“…Children with ROM or persistent OME have been shown also to exhibit insufficient antibody responses to pneumococcal polysaccharides of type 6A and 19F [4], P6 protein of NTHi [5,6], and CD protein of M. catarrhalis [8], and the poor response to these antigens has been attributed to their weak immunogenicity [26]. The anti-LTA antibody level showed only one hundredth fold levels of anti-whole cell body antibody, which concurred with results shown elsewhere [27,28], suggesting that the immunogenicity of LTA may be weak.…”
Section: Discussionmentioning
confidence: 99%
“…Selective immunologic failures against Streptococcus (S.) pneumoniae, nontypeable Haemophilus influenzae (NTHi) and Moraxella (M.) catarrhalis have been investigated widely in young children with recurrent acute otitis media (ROM) [4][5][6][7] and with persistent otitis media with effusion (OME) [8,9]. Lower antibody response to pneumococcal polysaccharides of type 6A and 19F has been demonstrated in infants and children with ROM [4].…”
Section: Introductionmentioning
confidence: 99%
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“…Because mortality due to LRTI (Schluger 2010) is more prevalent than that due to intracranial spread of middle ear infection (Monasta et al 2012, WHO 2004 First the pathogens causing rAOM are the same as those causing AOM (Pichichero 2000), but children prone to rAOM experience nasopharyngeal bacterial colonisation more frequently (Faden et al 1991, Harabuchi et al 1994 and with higher density (Stenfors & Raisanen 1992), although this may also be found in children with COME (Marchisio et al 2003)). Quantitative or qualitative defects in plasma immunoglobulins have been found in some, but not all, of those with rAOM (Freijd et al 1984, Freijd et al 1985, Harsten et al 1989, Hotomi et al 1999, Prellner et al 1984b, Stenfors & Raisanen 1993, Yamanaka & Faden 1993.…”
Section: Susceptibility To Raommentioning
confidence: 99%
“…Furthermore, AOM-associated immune responses to the major pathogens of AOM have been shown both in serum and in the middle ear [9][10][11], and the appearance of pathogen-specific serum and MEF antibodies has been associated with better recovery of AOM [12][13][14][15][16]. Additionally, an association between decreased immunoglobulin levels and recurrent AOM has been found in some cases [17,18]. Finally, the specific serum antibodies have been shown to protect from AOM both experimentally [19,20] and in children [21].…”
Section: Rationale For Vaccinationmentioning
confidence: 99%