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Divergent mucosal and systemic responses in children in response to acute otitis media
Author(s) -
Verhoeven D.,
Pichichero M. E.
Publication year - 2014
Publication title -
clinical & experimental immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.329
H-Index - 135
eISSN - 1365-2249
pISSN - 0009-9104
DOI - 10.1111/cei.12389
Subject(s) - immunology , immune system , otitis , streptococcus pneumoniae , population , cytokine , biology , haemophilus influenzae , medicine , microbiology and biotechnology , genetics , environmental health , antibiotics
Summary Acute otitis media ( AOM ), induced by respiratory bacteria, is a significant cause of children seeking medical attention worldwide. Some children are highly prone to AOMs , suffering three to four recurrent infections per year (prone). We previously determined that this population of children could have diminished anti‐bacterial immune responses in peripheral blood that could fail to limit bacterial colonization in the nasopharynx ( NP ). Here, we examined local NP and middle ear ( ME ) responses and compared them to peripheral blood to examine whether the mucosa responses were similar to the peripheral blood responses. Moreover, we examined differences in effector cytokine responses between these two populations in the NP , ME and blood compartments at the onset of an AOM caused by either S treptococcus pneumoniae or non‐typeable H aemophilus influenzae . We found that plasma effector cytokines patterned antigen‐recall responses of CD 4 T cells, with lower responses detected in prone children. ME cytokine levels did not mirror blood, but were more similar to the NP . Interferon ( IFN )‐γ and interleukin ( IL )‐17 in the NP were similar in prone and non‐prone children, while IL ‐2 production was higher in prone children. The immune responses diverged in the mucosal and blood compartments at the onset of a bacterial ME infection, thus highlighting differences between local and systemic immune responses that could co‐ordinate anti‐bacterial immune responses in young children.

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