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Anti-Nuclear Antibody Screening Using HEp-2 Cells
Published on: June 23, 2014
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Synthetic Nucleic Acid Antigens in Localized Scleroderma
Sangita Khatri1, Adrian H Bustos1, Christian Damsgaard Jørgensen2,3
1Department of Chemistry, Technical University of Denmark, 2800 Kongens Lyngby, Denmark.
International Journal of Molecular Sciences
|December 23, 2023
Summary
Synthetic nucleic acid antigen sequences impact autoimmune reactions in localized scleroderma. A specific DNA antigen, dsD4, strongly associated with disease activity, shows potential for early diagnostic tools in this autoimmune skin condition.
Area of Science:
- Immunology
- Dermatology
- Molecular Biology
Background:
- Localized scleroderma is an autoimmune skin disease.
- Anti-DNA antibodies are common in autoimmune conditions like lupus and localized scleroderma.
- The specific sequence of nucleic acid antigens may influence autoimmune responses.
Purpose of the Study:
- To investigate the impact of synthetic nucleic acid antigen sequences on autoantibody profiles in localized scleroderma.
- To determine if specific nucleic acid sequences correlate with disease activity.
- To explore potential diagnostic markers for localized scleroderma.
Main Methods:
- Synthesized a panel of DNA and RNA antigens.
- Performed autoantibody profiling in 70 children with localized scleroderma, healthy controls, and pediatric lupus patients.
- Utilized a bleomycin-induced mouse model to confirm in vivo findings.
Main Results:
- A synthetic DNA antigen, dsD4 (containing the BRAF oncogene sequence), showed a strong presence in localized scleroderma patients, unlike in systemic lupus erythematosus.
- dsD4 autoantibody levels significantly correlated with disease activity in localized scleroderma patients.
- In vivo administration of dsD4 induced a polyclonal response in a mouse model.
Conclusions:
- Nucleic acid antigen sequence specificity plays a role in localized scleroderma autoimmunity.
- dsD4 autoantibodies represent a potential biomarker for localized scleroderma.
- Findings suggest possibilities for novel early-stage diagnostic tools for localized scleroderma.

