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Neurology. 2019 Aug 1. pii: 10.1212/WNL.0000000000008061. doi: 10.1212/WNL.0000000000008061. [Epub ahead of print]

Autoimmune gait disturbance accompanying adaptor protein-3B2-IgG.

Author information

1
From the Departments of Laboratory Medicine and Pathology (J.A.H., T.J.K., S.R.H., V.A.L., S.J.P., C.J.K., A.M.), Neurology (A.S.L.-C., V.A.L., S.J.P., C.J.K., A.M.), and Immunology (V.A.L.), College of Medicine, Mayo Clinic, Rochester, MN; and Euroimmun, AG (L.K., M.S.), Lubeck, Germany.
2
From the Departments of Laboratory Medicine and Pathology (J.A.H., T.J.K., S.R.H., V.A.L., S.J.P., C.J.K., A.M.), Neurology (A.S.L.-C., V.A.L., S.J.P., C.J.K., A.M.), and Immunology (V.A.L.), College of Medicine, Mayo Clinic, Rochester, MN; and Euroimmun, AG (L.K., M.S.), Lubeck, Germany. mckeon.andrew@mayo.edu.

Abstract

OBJECTIVE:

To describe phenotypes, treatment response, and outcomes of autoimmunity targeting a synaptic vesicle coat protein, the neuronal (B2) form of adaptor protein-3 (AP3).

METHODS:

Archived serum and CSF specimens (from 616,025 screened) harboring unclassified synaptic antibodies mimicking amphiphysin-immunoglobulin G (IgG) on tissue-based indirect immunofluorescence assay (IFA) were re-evaluated for novel IgG staining patterns. Autoantigens were identified by western blot and mass spectrometry. Recombinant western blot and cell-binding assay (CBA) were used to confirm antigen specificity. Clinical data were obtained retrospectively.

RESULTS:

Serum (10) and CSF (6) specimens of 10 patients produced identical IFA staining patterns throughout mouse nervous system tissues, most prominently in cerebellum (Purkinje neuronal perikarya, granular layer synapses, and dentate regions), spinal cord gray matter, dorsal root ganglia, and sympathetic ganglia. The antigen revealed by mass spectrometry analysis and confirmed by recombinant assays (western blot and CBA) was AP3B2 in all. Of 10 seropositive patients, 6 were women; median symptom onset age was 42 years (range 24-58). Clinical information was available for 9 patients, all with subacute onset and rapidly progressive gait ataxia. Neurologic manifestations were myeloneuropathy (3), peripheral sensory neuropathy (2), cerebellar ataxia (2), and spinocerebellar ataxia (2). Five patients received immunotherapy; none improved, but they did not worsen over the follow-up period (median 36 months; range 3-94). Two patients (both with cancer) died. One of 50 control sera was positive by western blot only (but not by IFA or CBA).

CONCLUSION:

AP3B2 (previously named β-neuronal adaptin-like protein) autoimmunity appears rare, is accompanied by ataxia (sensory or cerebellar), and is potentially treatable.

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