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Published on: June 24, 2014
Frequency of autoantibodies in normal children
A Martini1, R Lorini, D Zanaboni
1Department of Pediatrics, University of Pavia, Italy.
Insights
Autoantibodies (AAs) are present in healthy children, with some remaining positive for two years. This suggests transient AA positivity is common in childhood.
Area of Science:
- Pediatrics
- Immunology
- Autoimmunity
Background:
- Limited data exist on autoantibody (AA) prevalence in healthy children.
- Autoimmune diseases often have an early onset, making pediatric studies crucial.
Purpose of the Study:
- To determine the frequency of 14 specific autoantibodies (AAs) in a cohort of apparently healthy children.
- To assess the persistence of detected AAs over a two-year period.
Main Methods:
- Investigated 14 autoantibodies in 268 children (aged 1 month to 14 years) with no history of autoimmune disease.
- Followed up 15 of the 41 positive children for AA presence and titer after two years.
Main Results:
- 41 out of 268 children (15.3%) tested positive for at least one AA, often at low titers.
- Common AAs included anti-gastric parietal cells (5.2%), antinuclear (3%), anti-smooth muscle (2.6%), and antireticulin (2.6%).
- Of 15 followed-up children, 6 (40%) remained positive for the same AA after two years, indicating transient positivity.
Conclusions:
- The frequency of AAs in healthy children is comparable to that in young adults.
- AA positivity in children is often transient, suggesting a dynamic immune system.
- Further research is needed to understand the long-term implications of pediatric AA positivity.
Abstract:
Very few data have been reported on the frequency of autoantibodies (AAs) in normal children. In the present study we investigated the frequency of 14 AAs in a total of 268 apparently normal children (151 boys and 117 girls; age range, 1 month to 14 years). Forty-one children (22 boys and 19 girls) were positive for at least one AA, usually in a low titer; two children were positive for two AAs. None of these children had a personal or family history of autoimmune diseases. The percentage of children positive for each AA was as follows: antinuclear, 3%; anti-smooth muscle, 2.6%; antireticulin, 2.6%; antimitochondrial, 1.1%; rheumatoid factor, 0.6%; antiribosomal, 0.4%; anti-gastric parietal cells, 5.2%; and anti-thyroid microsomal, 1.3%. Anti-double-stranded DNA, anti-intestinal epithelial cells, antiliver and antikidney microsomal, antithyroglobulin, anti-islet cells, and complement-fixing anti-islet cell antibodies were not detected in any serum. Fifteen of the 41 positive children were checked for the presence of AAs two years later; six (40%) were still positive, always for the same AA, without major differences in titer. Our results suggest that the overall frequency of AAs in apparently healthy children is quite similar to that reported in young adults; this AA positivity seems most often to represent a transient phenomenon.
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