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Factors influencing PCV13 specific antibody response in Danish children starting in day care
Sine Fjeldhøj1, Eva Fuglsang2, Camilla Adler Sørensen1
1Department of Bacteria, Parasites and Fungi, Statens Serum Institut, Copenhagen, Copenhagen, 2300, Denmark.
Insights
This study found that having siblings and Hepatitis B vaccination positively influenced the 13-valent pneumococcal conjugate vaccine (PCV13) antibody response in young children. Pneumococcal carriage did not affect this response.
Area of Science:
- Pediatrics
- Immunology
- Vaccinology
Background:
- The 13-valent pneumococcal conjugate vaccine (PCV13) is crucial for preventing pneumococcal disease.
- Factors influencing PCV13-specific antibody response in children attending day care require further investigation.
Purpose of the Study:
- To identify factors affecting the PCV13 antibody response in Danish children aged 8-13 months.
- To explore the relationship between pneumococcal carriage, host factors, and vaccine response.
Main Methods:
- Secondary analysis of the ProbiComp study involving nose/buccal swabs and blood samples.
- Pneumococcal serotyping using latex agglutination and Quellung reaction.
- Antibody quantification via Luminex assay and gene expression analysis (qPCR).
Main Results:
- PCV13 antibody response was not influenced by pneumococcal serotype carriage.
- Having siblings was associated with increased PCV13 antibody response (p=0.0135).
- Hepatitis B vaccination was linked to a higher PCV13 antibody response before day care (p=0.005).
Conclusions:
- Sibling presence and prior Hepatitis B vaccination are associated with enhanced PCV13 immunogenicity.
- Investigating host-related factors can inform vaccination strategies for young children.
Abstract:
This study examines different factors influencing the 13-valent pneumococcal conjugate vaccine (PCV13) specific antibody response in 8-13 months old Danish children starting in day care. We present secondary findings to the ProbiComp study, which included nose swabs, buccal swabs and blood samples from the children before entering day care (baseline) and again after 6 months. Pneumococci isolated from nose swabs were identified by latex agglutination kit and Quellung reaction. Luminex-based assay was used for antibody measurements against specific anti-pneumococcal capsular IgG. Buccal gene expression was analyzed by qPCR. Statistical analyses were performed in R and included Pearson's Chi-squared test, Welch two sample t-test and linear regression models. The PCV13 antibody response was unaffected by whether the children were carriers or non-carriers of any pneumococcal serotype. Having siblings increased the risk of carrying serotype 21 before day care (p = 0.020), and having siblings increased the PCV13 antibody response at the end of study (p = 0.0135). Hepatitis B-vaccination increased the PCV13 antibody response before day care attendance (p = 0.005). The expression of IL8 and IL1B was higher in children carrying any pneumococcal serotype at baseline compared to non-carriers (p = 0.0125 and p = 0.0268 respectively).
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