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Specific antibody deficiency in children with recurrent respiratory infections: a controlled study with follow-up
O Ruuskanen1, A Nurkka, M Helminen
1Department of Paediatrics, Turku University Hospital, PO Box 52, FI-20521 Turku, Finland. olli.ruuskanen@tyks.fi
Insights
Specific antibody deficiency (SAD) to pneumococcal vaccine is common in children with recurrent infections. Many children with SAD recover within a few years without treatment, indicating a transient condition.
Area of Science:
- Immunology
- Pediatrics
Background:
- Specific antibody deficiency (SAD) to unconjugated pneumococcal vaccine (PPV) is a known primary B cell immunodeficiency.
- The prevalence and long-term course of SAD in pediatric populations are not well understood.
Purpose of the Study:
- To investigate the occurrence and natural history of SAD in children experiencing recurrent respiratory infections.
- To assess the immune response to PPV in children with recurrent infections compared to healthy controls.
Main Methods:
- An observational study involving 99 children with recurrent/severe infections vaccinated with PPV.
- Serum antibody concentrations were measured pre- and post-vaccination using enzyme immunoassay.
- A retrospective control group of 89 age- and gender-matched healthy children was included.
Main Results:
- 11% of children with recurrent respiratory infections exhibited SAD.
- Children with SAD often presented with additional minor immune defects.
- Most children with SAD showed spontaneous recovery within 3.8 years without immunoglobulin replacement therapy.
Conclusions:
- SAD is a relatively common condition in young children with recurrent respiratory infections.
- SAD in children is frequently transient, with many cases resolving spontaneously over time.
- The findings suggest that careful monitoring, rather than immediate intervention, may be appropriate for pediatric SAD.
Abstract:
Specific antibody deficiency (SAD) to unconjugated pneumococcal vaccine (PPV) is an established primary B cell immunodeficiency. The occurrence and natural history of SAD in children is unclear. We conducted an observational study to identify SAD in children with recurrent respiratory infections. Ninety-nine children, mean age 5·9 (range 2-16) years, with recurrent or severe infections were vaccinated with PPV; serum antibody concentrations for serotypes 4, 6B, 9V, 14, 18C, 19F and 23F were measured before and 2 weeks after vaccination with enzyme immunoassay. The retrospective control group consisted of 89 healthy children matched for age and gender. No children had received previous conjugated pneumococcal vaccine (PCV) or PPV. The structured history of infectious diseases of all participants was collected. Ten of 91 (11%) children (eight excluded due to immunoglobulin G subclass deficiency) with recurrent respiratory infections had SAD. In the control group, three children (3%) responded inadequately to PPV (P = 0·05). Most children with SAD also had many other minor immune defects. After 0·5-5 years (medium 3·8), eight children with SAD were revaccinated with PPV; five responded adequately and three inadequately. Two SAD children were revaccinated with PCV, one developed an adequate and one an inadequate response. Two children with SAD received treatment with intravenous immunoglobulin; the remaining eight children recovered without replacement therapy during the follow-up. SAD is common in young children with recurrent respiratory infections, but it is often transient and resolves itself within a few years without specific treatment.
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