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Published on: February 23, 2014
Non-linear relationships between children age and pneumococcal vaccine coverage: Important implications for vaccine
Yanling Liu1, Wenhui Li1, Qian Dong1
1School of Public Health, Guangdong Pharmaceutical University, Guangzhou, China.
Insights
High pneumococcal conjugate vaccine (PCV) coverage in children is achieved at age 2 years and older. This study also supports ply and lytA as key targets for new protein vaccines against Streptococcus pneumoniae infections.
Area of Science:
- Microbiology and Immunology
- Vaccinology
- Pediatric Infectious Diseases
Background:
- Streptococcus pneumoniae (S. pneumoniae) is a major cause of childhood illness and death globally.
- Understanding factors influencing vaccine effectiveness and pathogen characteristics is crucial for public health.
- This study investigates S. pneumoniae in children, focusing on age, vaccine coverage, and pathogen traits.
Purpose of the Study:
- To determine the relationship between age and pneumococcal vaccine coverage in children.
- To explore correlations between age and vaccine coverage for various vaccine types (capsular, protein, pilus-based).
- To analyze the links between multiple phenotype-genotype characteristics of S. pneumoniae isolates.
Main Methods:
- S. pneumoniae isolates were analyzed for antimicrobial susceptibility, virulence genes, serotypes, and sequence types.
- Restricted cubic spline models were employed to assess age-related vaccine coverage.
- Phenotype-genotype characteristics were correlated with isolate data.
Main Results:
- 13-valent pneumococcal conjugate vaccine (PCV13) showed high coverage (85.8%).
- Non-linear relationships between age and vaccine coverage (PCV7, PCV10, PCV13) were observed, with fluctuations in children under 2 years.
- Stable, high coverage for ply and lytA (protein/pilus vaccine candidates) was noted across all ages, alongside complex phenotype-genotype correlations (e.g., ST271 with serotype 19F).
Conclusions:
- Optimal pneumococcal conjugate vaccine (PCV) coverage is achieved in children aged 2 years and older.
- The findings support ply and lytA as priority targets for next-generation protein vaccines.
- Understanding these relationships can guide vaccine development and public health strategies.
Background:
Streptococcus pneumoniae (S. pneumoniae) is an important pathogen causing both invasive and non-invasive infections in children, with significant morbidity and mortality worldwide. This study aimed to determine the potential relationships between age and vaccine coverage and between multiple phenotype-genotype characteristics of S. pneumoniae isolated from children.
Methods:
All S. pneumoniae isolates were tested for antimicrobial susceptibility, virulence genes, serotypes, and sequence types. The restricted cubic spline models were used to reveal potential relationships between children age and pneumococcal vaccine coverage.
Results:
For capsular-based vaccines, we observed a high coverage rate of 13-valent pneumococcal conjugate vaccine (PCV13, 85.8%) and a significantly non-linear relationship between children age and vaccine coverage (including PCV7, PCV10, and PCV13), with marked fluctuations in children aged < 2 years. For protein-based and pilus-based vaccine candidates, we demonstrated dynamic non-linear relationships between age and vaccine coverage, maintaining a stable and high coverage rate of ply and lytA for all age groups. Moreover, there were significantly high-dimensional corresponding relationships among multiple phenotype-genotype characteristics of S. pneumoniae isolates (such as ST271 associated with serotype 19F, PI-2, and extensively drug-resistance).
Conclusions:
Our findings suggest that the age for high PCV coverage being children aged ≥ 2 years and also provide important evidence for supporting ply and lytA as priority candidate targets for the development of new-generation protein vaccines.
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