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Response to pneumococcal conjugate and polysaccharide vaccination in children with rheumatic disease
Lotte Jensen1,2, Anne Estmann Christensen3, Susan Nielsen1
1The Department of Paediatrics and Adolescent Medicine, Juliane Marie Centre, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.
Insights
Children with rheumatic disease and compromised immune systems show a positive response to pneumococcal immunization. This study confirms that the 13-valent pneumococcal conjugate vaccine followed by the 23-valent pneumococcal polysaccharide vaccine is effective in this vulnerable group.
Area of Science:
- Immunology
- Pediatrics
- Rheumatology
Background:
- Children with rheumatic diseases often have compromised immune systems, increasing their susceptibility to infections.
- Streptococcus pneumoniae is a common pathogen in this population, making immunization crucial.
Purpose of the Study:
- To evaluate the immunogenicity of pneumococcal vaccination in immunocompromised children with rheumatic disease.
- To assess the response to a sequential vaccination schedule using 13-valent pneumococcal conjugate vaccine (PCV13) followed by 23-valent pneumococcal polysaccharide vaccine (PPSV23).
Main Methods:
- A cohort of 27 children (aged 2-19 years) with rheumatic disease and compromised immunity received PCV13 followed by PPSV23.
- Blood samples were collected pre-vaccination and post-vaccination to quantify IgG antibodies against 12 pneumococcal serotypes.
- Seroprotection was defined as IgG antibody levels ≥0.35 µg/mL.
Main Results:
- Following PCV13, significant increases in antibody titers were observed for 9 out of 12 serotypes compared to pre-vaccination levels.
- After PPSV23, antibody titers increased for most serotypes, though not reaching statistical significance.
- The odds of achieving seroprotection increased after PCV13 for 10/12 serotypes, with significance for three.
Conclusions:
- Immunocompromised children with rheumatic disease mount an immune response to pneumococcal immunization.
- The sequential PCV13 followed by PPSV23 vaccination strategy appears effective in inducing and maintaining protective antibody levels in this patient group.
Abstract:
Children with rheumatic disease and compromised immune system have an increased risk of infection. Streptococcus pneumoniae is a frequent pathogen, and immunization is recommended. In this study, we investigated whether immunocompromised children with rheumatic disease do respond to pneumococcal immunization with 13-valent pneumococcal conjugate vaccine followed by 23-valent pneumococcal polysaccharide vaccine. The study was conducted at two tertiary referral hospitals in Denmark from 2015 to 2018. Patients with rheumatic disease and compromised immune system aged 2-19 years were eligible. Patients were vaccinated with 13-valent pneumococcal conjugate vaccine followed by 23-valent pneumococcal polysaccharide vaccine. A blood sample was collected before vaccination and after each vaccination. IgG antibodies were quantified for twelve serotypes. Seroprotection for each serotype was defined as IgG ≥0.35 µg/mL. A total of 27 patients were enrolled. After the conjugate vaccine, an increase in antibody titres compared with pre-vaccination was found for all serotypes and 9/12 were significant. After the polysaccharide vaccine, the antibody titres for all serotypes but one was seen to increase but none reached significance. The proportion of patients protected before immunization ranged from 20.8% to 100% for the individual serotypes. Odds ratio for achieving seroprotection after the conjugate vaccine was >1 for 10/12 serotypes but only significant for three serotypes. After the polysaccharide vaccine, the odds ratio was >1 for 9/12 serotypes but none reached significance. In conclusion, children with rheumatic disease and compromised immune system respond to pneumococcal immunization with 13-valent pneumococcal conjugate vaccine and maintain antibody levels upon subsequent immunization with 23-valent pneumococcal polysaccharide vaccine.
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