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Signal Attenuation as a Rat Model of Obsessive Compulsive Disorder
Published on: January 9, 2015
Incidence of anti-brain antibodies in children with obsessive-compulsive disorder
Russell C Dale1, Isobel Heyman, Gavin Giovannoni
1Department of Child and Adolescent Psychiatry, PO Box 085, Institute of Psychiatry, De Crespigny Park, London SE5 8AF, UK.
Insights
Children with obsessive-compulsive disorder (OCD) show elevated anti-basal ganglia antibodies (ABGA), suggesting a link to post-streptococcal autoimmunity. This supports autoimmunity as a potential cause in some OCD cases.
Area of Science:
- Neuroscience
- Immunology
- Pediatrics
Background:
- Obsessive-compulsive disorder (OCD) shares symptoms with post-streptococcal disorders like Sydenham's chorea and PANDAS.
- Anti-basal ganglia antibodies (ABGA) are implicated as potential mediators in these conditions.
Purpose of the Study:
- To investigate the role of post-streptococcal autoimmunity in idiopathic OCD.
- To test the hypothesis that ABGA may be involved in the development of OCD.
Main Methods:
- Examined 50 children diagnosed with OCD for the presence of ABGA.
- Utilized enzyme-linked immunosorbent assay (ELISA) and western immunoblotting techniques.
- Compared findings with autoimmune, neurological, and streptococcal control groups.
Main Results:
- ELISA showed significantly elevated mean ABGA binding in OCD patients compared to all control groups (P<0.005).
- Western immunoblotting detected positive antibody binding in 42% of OCD patients, versus 2-10% in controls (P<0.001).
- Antibody binding patterns in OCD patients resembled those seen in Sydenham's chorea.
Conclusions:
- Findings suggest that central nervous system autoimmunity may contribute to a significant subset of OCD cases.
- Further research is warranted to determine if these antibodies are pathogenic in OCD.
- The study supports a potential autoimmune mechanism underlying some pediatric OCD presentations.
Background:
Obsessions and compulsions may occur in the post-streptococcal disorders Sydenham's chorea and paediatric autoimmune neuropsychiatric disorders associated with streptococcus (PANDAS). The proposed mediators are anti-basal ganglia antibodies (ABGA).
Aims:
We tested the hypothesis that post-streptococcal autoimmunity may have a role in'idiopathic'obsessive-compulsive disorder (OCD).
Method:
We examined 50 children with OCD for ABGA using enzyme-linked immunosorbent assay (ELISA) and western immunoblotting. The findings were compared with paediatric autoimmune (n=50), neurological (n=100) and streptococcal (n=40) controls.
Results:
The mean ABGA binding on ABGA binding on ELISA was elevated in the patient cohort compared with all control groups (P<0.005 in all comparisons). Western immunoblotting revealed positive antibody binding (as seen in Sydenham's chorea) in 42% of the patient cohort compared with 2-10% of control groups (P<0.001 in all comparisons).
Conclusions:
Our findings support the hypothesis that central nervous system autoimmunity may have a role in a significant subgroup of cases of OCD. Further study is required to examine whether the antibodies concerned are pathogenic.
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