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.

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