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Published on: August 7, 2017
Atopic eczema is associated with delayed maturation of the antibody response to pneumococcal vaccine
P D Arkwright1, L Patel, A Moran
1University Department of Child Health, Booth Hall Children's Hospital, and Immunology Department, Hope Hospital, Manchester, UK. peter_arkwright@lineone.net
Insights
Children with atopic eczema under 9 years old show a poor antibody response to Pneumococcal vaccination. This suggests a potential delay in immune system maturation for these young patients.
Area of Science:
- Immunology
- Pediatrics
- Dermatology
Background:
- Atopic eczema is a common condition in children.
- Antibody response to vaccines is crucial for preventing infections.
- Previous observations suggested impaired immunity in children with atopic eczema.
Purpose of the Study:
- To investigate the antibody response to Pneumococcal vaccination in children under 9 with atopic eczema.
- To compare this response with a control group of children with recurrent respiratory infections.
- To identify potential immune system maturation delays.
Main Methods:
- Retrospective study of 35 children with moderate to severe atopic eczema (ages 3-16).
- Comparison with 36 control children (ages 3-16) with recurrent upper respiratory tract infections.
- Analysis of Pneumococcal antibody responses after Pneumovax II immunization.
Main Results:
- Only 17% of children with atopic eczema (ages 3-8) responded to Pneumovax, significantly lower than controls (57%).
- No significant differences in total IgG2 levels were found between groups.
- A delayed maturation of antibody response to Pneumococcus was observed in children with atopic eczema.
Conclusions:
- Children with atopic eczema under 9 years exhibit a poorer antibody response to Pneumococcal vaccination.
- This impaired response may indicate a delay in immune system maturation.
- Further research is needed to understand the implications for infection susceptibility.
Abstract:
The aim of this study was to investigate a previously undocumented observation, that children with atopic eczema under 9 years of age tended to have a poor antibody response to Pneumococcal vaccination. Thirty-five children (mean age 8.8 years, range 3-16 years) with moderate to severe atopic eczema but no history of systemic infection were studied retrospectively. Pneumococcal antibody responses after immunization with Pneumovax II were compared with a hospital control group consisting of 36 children (mean age 6.0 years, range 3-16 years) with recurrent upper respiratory tract infections. Only 17% of children with atopic eczema aged 3-8 years responded to Pneumovax. This response was significantly poorer than that of the controls (57%) (odds ratio 0.20, 95% confidence interval (CI) 0.05-0.84, P = 0.03). There were no significant differences in the levels of total IgG2, the component of IgG associated with protective antibody responses to Pneumococcus between the two groups. Delay in maturation of the total IgG and IgG2 antibody response to Pneumococcus is a feature in this group of children with moderately severe atopic eczema.
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