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Antinuclear antibodies in children with localized scleroderma
A M Rosenberg1, Y Uziel, B R Krafchik
1Department of Pediatrics, University of Saskatchewan, Saskatoon, Canada.
The Journal of Rheumatology
|December 1, 1995
Summary
Antinuclear antibodies (ANA) are common in children with localized scleroderma, often targeting denatured DNA (dDNA) and high mobility group (HMG) proteins. This contrasts with systemic sclerosis, where other autoantibodies are more prevalent.
Area of Science:
- Pediatric Rheumatology
- Immunology
- Dermatology
Background:
- Localized scleroderma is a connective tissue disease affecting children.
- Antinuclear antibodies (ANA) are autoantibodies associated with autoimmune diseases.
- Understanding ANA profiles in pediatric localized scleroderma is crucial for diagnosis and management.
Purpose of the Study:
- To investigate the prevalence of ANA in children diagnosed with localized scleroderma.
- To identify the specific antigenic targets of ANA in this pediatric population.
- To compare ANA findings in localized scleroderma with those in systemic sclerosis.
Main Methods:
- Sera from 27 children with localized scleroderma were analyzed.
- Indirect immunofluorescence was used to detect ANA.
- ELISA and immunoblotting assays identified specific nuclear antigen reactivity, including denatured DNA (dDNA), high mobility group (HMG) proteins, histones, and topoisomerase I.
Main Results:
- 63% of children with localized scleroderma tested positive for ANA.
- Antibodies to denatured DNA (dDNA) were found in 56% of sera, and antibodies to high mobility group (HMG) proteins in 41%.
- Antibodies to histones and topoisomerase I were less common (15% and 4%, respectively).
Conclusions:
- ANA are prevalent in childhood localized scleroderma, frequently directed against dDNA and HMG proteins.
- The ANA profile in localized scleroderma shares similarities with systemic sclerosis, particularly regarding dDNA antibodies.
- Childhood localized scleroderma is less commonly associated with specific nuclear and nucleolar autoantibodies typical of systemic sclerosis.