Antibodies to dendritic neuronal surface antigens in opsoclonus myoclonus ataxia syndrome.

Abstract:

:Opsoclonus myoclonus ataxia syndrome (OMAS) is an autoimmune disorder characterized by rapid, random, conjugate eye movements (opsoclonus), myoclonus, and ataxia. Given these symptoms, autoantibodies targeting the cerebellum or brainstem could mediate the disease or be markers of autoimmunity. In a subset of patients with OMAS, we identified such autoantibodies, which bind to non-synaptic puncta on the surface of live cultured cerebellar and brainstem neuronal dendrites. These findings implicate autoimmunity to a neuronal surface antigen in the pathophysiology of OMAS. Identification of the targeted antigen(s) could elucidate the mechanisms underlying OMAS and provide a biomarker for diagnosis and response to therapy.

journal_name

J Neuroimmunol

authors

Panzer JA,Anand R,Dalmau J,Lynch DR

doi

10.1016/j.jneuroim.2015.07.007

subject

Has Abstract

pub_date

2015-09-15 00:00:00

pages

86-92

eissn

0165-5728

issn

1872-8421

pii

S0165-5728(15)30009-6

journal_volume

286

pub_type

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