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No evidence for impaired humoral immunity to pneumococcal proteins in Australian Aboriginal children with otitis media. | LitMetric

No evidence for impaired humoral immunity to pneumococcal proteins in Australian Aboriginal children with otitis media.

Int J Pediatr Otorhinolaryngol

School of Paediatrics and Child Health, The University of Western Australia, GPO Box D184, Perth, Western Australia, 6840, Australia; Telethon Kids Institute, The University of Western Australia, 100 Roberts Road, Subiaco, Western Australia, 6008, Australia; Department of Otorhinolaryngology, Princess Margaret Hospital for Children, Roberts Road, Subiaco, Western Australia, 6008, Australia. Electronic address:

Published: January 2017

AI Article Synopsis

  • Australian Aboriginal children have high rates of otitis media (OM), with Streptococcus pneumoniae being a primary cause and no effective vaccine available.
  • A study examined the antibody responses to certain S. pneumoniae antigens in 183 children, including Aboriginal and non-Aboriginal groups, to understand their immune response to OM.
  • Results showed that Aboriginal children with a history of OM had higher antibody levels than non-Aboriginal healthy children, indicating that they respond well to potential vaccine candidates for S. pneumoniae.

Article Abstract

Background: The Australian Aboriginal population experiences disproportionately high rates of otitis media (OM). Streptococcus pneumoniae is one of the main pathogens responsible for OM and currently no vaccine offering cross strain protection exists. Vaccines consisting of conserved antigens to S. pneumoniae may reduce the burden of OM in high-risk populations; however no data exists examining naturally acquired antibody in Aboriginal children with OM.

Methods: Serum and salivary IgA and IgG were measured against the S. pneumoniae antigens PspA1 and 2, CbpA and Ply in a cross sectional study of 183 children, including 36 non-Aboriginal healthy control children and 70 Aboriginal children and 77 non-Aboriginal children undergoing surgery for OM using a multiplex bead assay.

Results: Significant differences were observed between the 3 groups for serum anti-PspA1 IgA, anti-CbpA and anti-Ply IgG and for all salivary antibodies assessed. Aboriginal children with a history of OM had significantly higher antibody titres than non-Aboriginal healthy children with no history of OM and non-Aboriginal children with a history of OM for several proteins in serum and saliva. Non-Aboriginal children with a history of OM had significantly higher salivary anti-PspA1 IgG than healthy children, while all other titres were comparable between the groups.

Conclusions: Conserved vaccine candidate proteins from S. pneumoniae induce serum and salivary antibody responses in Aboriginal and non-Aboriginal children with a history of OM. Aboriginal children do not have an impaired antibody response to the antigens measured from S. pneumoniae and they may represent vaccine candidates in Indigenous populations.

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Source
http://dx.doi.org/10.1016/j.ijporl.2016.11.019DOI Listing

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