Pneumococcal infection in children with recurrent respiratory diseases

Пневмококковая инфекция у детей с рецидивирующими респираторными заболеваниями
И. В. Бабаченко, Л. И. Железова, E. A. Kozyrev, Ekaterina Nikitina, N. S. Tian
2024-09-24

local mucosal immunitynasopharyngeal microbiocenosispneumococcal conjugate vaccinespneumococcal serotypesrecurrent respiratory diseases
In frequently ill children with recurrent respiratory diseases (RRD), violations of local immunity and microbiocenosis of the mucous membranes can contribute to the development of acute and chronic bronchopulmonary diseases. Vaccination against major pathogens, including S. pneumoniae, can help prevent respiratory infections in children.Objective: to study the microbiocenosis and local immunological factors of the nasopharyngeal mucosa in children with RRD, the serotype composition of S. pneumoniae in children with community-acquired pneumococcal pneumonia (CAP) and pneumococcal carriers, as well as the correspondence of the serotype landscape to the composition of modern pneumococcal vaccines.Materials and methods: The study included 150 patients (104 children with RRD and 46 patients with CAP). To assess the condition of the nasopharyngeal mucosa cultural methods, morphofunctional, immunological and capsule PCR typing of S. pneumoniae isolates were performed. Statistical analysis was performed using the Statistica 10.0 package.Results: The age structure was dominated by children aged 3 to 6 years (36%). The majority of patients with RRD had pronounced nasopharyngeal mucosal dysbiosis (n=60), as well as destruction of epithelial cells (n=97). These factors may predispose to the development of bronchopulmonary diseases, including community-acquired pneumonia (CAP). Capsule PCR typing of S. pneumoniae isolates from the nasopharynx was performed in 46 patients. It has been established that in the structure of nasopharyngeal carrier S. pneumoniae in children with CAP, serotypes “3” and 19F prevailed, which were also the main pathogens in pneumococcal CAP. In nasopharyngeal pneumococcal carrier, the thirteen–valent pneumococcal conjugate vaccine (PCV13) overlapped 39.6% (95%CI 27.6–53.1%) of serotypes, in pneumococcal VP – 57.2% (95% CI 36.5-75.5%), while PCV20 overlapped 22.6% more S. pneumoniae serotypes in children with CAP.Conclusion: The strategy for the prevention of acute respiratory infections in children is immunization against pneumococcal infection, which should be carried out taking into account the regional prevalence of S. pneumoniae serotypes.
1
Among children with community-acquired pneumococcal pneumonia, pneumococcal serotypes 3 and 19F predominated in both nasopharyngeal carriage and pneumonia.
2
Children with recurrent respiratory diseases frequently exhibited pronounced nasopharyngeal dysbiosis and epithelial-cell destruction, potentially predisposing them to bronchopulmonary disease.
3
PCV13 covered 39.6% of carried pneumococcal serotypes and 57.2% of serotypes causing pneumococcal pneumonia in the studied children.
4
PCV20 covered 22.6% more pneumococcal serotypes in children with community-acquired pneumonia than PCV13.
5
The study characterized nasopharyngeal microbiocenosis, local immune factors, and pneumococcal serotypes in children with recurrent respiratory diseases and pneumococcal pneumonia.

Nasopharyngeal microbiocenosis and Streptococcus pneumoniae infection in children with recurrent respiratory diseases and community-acquired pneumococcal pneumonia

Nasopharyngeal dysbiosis and local immune factors, S. pneumoniae serotype distribution, and coverage by pneumococcal vaccines

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2024-09-24
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И. В. Бабаченко
Л. И. Железова
E. A. Kozyrev
Ekaterina Nikitina
N. S. Tian
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