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Distinct patterns of serum immunoreactivity as evidence for multiple brain-directed autoantibodies in juvenile neuronal ceroid lipofuscinosis
M. J. Lim*, J. Beake*, E. Bible*, T. M. Curran, D. Ramirez-Montealegre, D. A. Pearce†‡§ and J. D. Cooper*
  *Pediatric Storage Disorders Laboratory, Centre for the Cellular Basis of Behaviour, Department of Neuroscience, MRC Social Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, King's College London, De Crespigny Park, London, UK,   Center for Ageing and Developmental Biology,   Department of Neurology, and   §Department of Biochemistry and Biophysics, University of Rochester School of Medicine and Dentistry, University of Rochester, Rochester, NY, USA
Correspondence to  Jonathan D. Cooper, Pediatric Storage Disorders Laboratory, Centre for the Cellular Basis of Behaviour, Department of Neuroscience, Box P040, MRC Social Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, King's College London, De Crespigny Park, London SE5 8AF, UK. Tel: +44 20 7848 0286; Fax: +44 20 7848 0273; E-mail: j.cooper@iop.kcl.ac.uk
Copyright 2006 Blackwell Publishing Ltd
KEYWORDS
autoantibodies • autoimmunity • Batten disease • immunoreactivity • neuronal ceroid lipofuscinoses • patient-derived sera
M. J. Lim, J. Beake, E. Bible, T. M. Curran, D. Ramirez-Montealegre, D. A. Pearce and J. D. Cooper (2006) Neuropathology and Applied Neurobiology 32, 469–482
Distinct patterns of serum immunoreactivity as evidence for multiple brain-directed autoantibodies in juvenile neuronal ceroid lipofuscinosis

ABSTRACT

Autoantibodies to glutamic acid decarboxylase (GAD65) have been reported in sera from the Cln3–/– mouse model of juvenile neuronal ceroid lipofuscinosis (JNCL), and in individuals with this fatal paediatric neurodegenerative disorder. To investigate the existence of other circulating autoreactive antibodies, we used sera from patients with JNCL and other forms of neuronal ceroid lipofuscinosis (NCL) as primary antisera to stain rat and human central nervous system sections. JNCL sera displayed characteristic patterns of IgG, but not IgA, IgE or IgM immunoreactivity that was distinct from the other forms of NCL. Immunoreactivity of JNCL sera was not confined to GAD65-positive (GABAergic) neurons, but also stained multiple other cell populations. Preadsorption of JNCL sera with recombinant GAD65 reduced the intensity of the immunoreactivity, but did not significantly change its staining pattern. Moreover, sera from Stiff Person Syndrome and Type I Diabetes, disorders in which GAD65 autoantibodies are present, stained with profiles that were markedly different from JNCL sera. Collectively, these studies provide evidence of the presence of autoreactive antibodies within multiple forms of NCL, and are not exclusively directed towards GAD65.


Received 14 September 2005 Accepted after revision 24 January 2006

DIGITAL OBJECT IDENTIFIER (DOI)
10.1111/j.1365-2990.2006.00738.x About DOI

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