Differential binding of antibodies in PANDAS patients to cholinergic interneurons in the striatum
Luciana R Frick1, Maximiliano Rapanelli1, Kantiya Jindachomthong1
1Department of Psychiatry, Yale University, United States.
Insights
Antibodies in children with Pediatric Autoimmune Neuropsychiatric Disorder Associated with Streptococcus (PANDAS) specifically target cholinergic interneurons in the brain. This binding decreased with symptom improvement after treatment, suggesting a key role in PANDAS.
Area of Science:
- Neuroscience
- Immunology
- Pediatrics
Background:
- Pediatric Autoimmune Neuropsychiatric Disorder Associated with Streptococcus (PANDAS) is characterized by acute onset of neuropsychiatric symptoms following Group A beta-hemolytic Streptococcus infection.
- The underlying pathophysiology of PANDAS is not fully understood, with theories suggesting autoimmune cross-reactivity against brain antigens.
Purpose of the Study:
- To investigate the specific cellular targets of antibodies in the serum of children with PANDAS.
- To explore the role of striatal interneurons, implicated in tic disorders, as potential targets.
Main Methods:
- Development of an in vivo mouse model to assess antibody binding in the striatum.
- Infusion of serum from PANDAS patients and controls into mouse striata.
- Characterization of antibody binding to interneurons using immunofluorescence and confocal microscopy.
Main Results:
- Antibodies from PANDAS patients showed significantly higher binding to cholinergic interneurons (∼80%) compared to controls (<50%).
- No elevated binding was observed in two populations of GABAergic interneurons (PV and nNOS-positive), indicating specificity.
- Increased binding to cholinergic interneurons resolved following intravenous immunoglobulin treatment, correlating with symptom improvement.
Conclusions:
- Antibody-mediated targeting of striatal cholinergic interneurons represents a potential mechanism of pathology in PANDAS.
- Further research into the functional consequences of this specific antibody binding could reveal new therapeutic targets for PANDAS.
Abstract:
Pediatric Autoimmune Neuropsychiatric Disorder Associated with Streptococcus, or PANDAS, is a syndrome of acute childhood onset of obsessive-compulsive disorder and other neuropsychiatric symptoms in the aftermath of an infection with Group A beta-hemolytic Streptococcus (GABHS). Its pathophysiology remains unclear. PANDAS has been proposed to result from cross-reactivity of antibodies raised against GABHS with brain antigens, but the targets of these antibodies are unclear and may be heterogeneous. We developed an in vivo assay in mice to characterize the cellular targets of antibodies in serum from individuals with PANDAS. We focus on striatal interneurons, which have been implicated in the pathogenesis of tic disorders. Sera from children with well-characterized PANDAS (n = 5) from a previously described clinical trial (NCT01281969), and matched controls, were infused into the striatum of mice; antibody binding to interneurons was characterized using immunofluorescence and confocal microscopy. Antibodies from children with PANDAS bound to ∼80% of cholinergic interneurons, significantly higher than the <50% binding seen with matched healthy controls. There was no elevated binding to two different populations of GABAergic interneurons (PV and nNOS-positive), confirming the specificity of this phenomenon. Elevated binding to cholinergic interneurons resolved in parallel with symptom improvement after treatment with intravenous immunoglobulin. Antibody-mediated dysregulation of striatal cholinergic interneurons may be a locus of pathology in PANDAS. Future clarification of the functional consequences of this specific binding may identify new opportunities for intervention in children with this condition.
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