Frequencies of neuronal autoantibodies in healthy controls
Estimation of disease specificity
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Abstract
Objective: To provide an extensive overview on the prevalence of antibodies against neuronal surfaces (neuronal surface antibody [NSAb]) in healthy participants and disease controls.
Methods: We searched the PubMed database (1974 to October 2016) for studies that analyzed frequencies of 22 different NSAbs in serum or CSF and included controls. Antibody prevalence was calculated for patients with NSAb-mediated disease and controls, including healthy participants, and those with neurologic and nonneurologic diseases. Different assays for antibody detection were compared.
Results: In 309 articles, 743,299 antibody tests for 22 NSAbs were performed, including 30,485 tests for 19 NSAbs in healthy controls (HCs). Of these, 26,423 (86.7%) were tested with current standard methods, usually cell-based assays. Prevalence was very low in HCs (mean 0.23%, absent for 9/19 antibodies), and test numbers ranged from 21 to 3,065 per antibody. One study reported >1,000 healthy participants, and the others contained 21–274 samples. CSF samples were virtually not available from HCs. NSAb prevalence was considerably higher (1.5%) in 69,850 disease controls, i.e., patients not initially suspected to have NSAb-mediated diseases. Antibody determination in controls using nonstandard assays (such as ELISA) resulted in 6% positivity.
Conclusions: NSAbs are rarely found in healthy participants, particularly with standard detection methods, suggesting high disease specificity and supporting their diagnostic usefulness. Conversely, positive titers in atypical patients might point to the still expanding phenotypic spectrum. Future studies should include more CSF samples, data from HCs, and experimental evidence for antibody pathogenicity.
GLOSSARY
- AMPAR1/2, AMPAR3=
- alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor subunits 1/2 and 3;
- AQP4=
- aquaporin-4;
- Caspr2=
- contactin-associated protein-like 2;
- CBA=
- cell-based assay;
- D2R=
- dopamine-2 receptor;
- DNER=
- delta/notch-like epidermal growth factor–related receptor;
- DPPX=
- dipeptidyl-peptidase-like protein 6;
- FACS=
- fluorescence-activated cell sorting;
- GABAaR and GABAbR=
- gamma-aminobutyric acid-A and -B receptor;
- GlyR=
- glycine receptor;
- HC=
- healthy control;
- IgLON5=
- cell adhesion molecule IgLON family member 5;
- IHC=
- immunohohstochemistry;
- Lgi1=
- leucine-rich glioma-inactivated protein 1;
- mGluR5=
- metabotropic glutamate receptor 5;
- MOG=
- myelin oligodendrocyte glycoprotein;
- nAChR (m), nAChR (g)=
- nicotinic acetylcholine receptor of muscle (m) and ganglionic (g) type;
- NMDAR/NR1, NMDAR/NR2=
- N-methyl-D-aspartate-receptor subunits NR1 or NR2;
- NSAb=
- neuronal surface antibody;
- PRG5=
- plasticity-related gene 5;
- RIA=
- radioimmunoassay;
- VGKC=
- voltage-gated potassium channel;
- WB=
- Western blot
Footnotes
Funding information and disclosures are provided at the end of the article. Go to Neurology.org/nn for full disclosure forms. The Article Processing Charge was funded by German Center for Neurodegenerative Diseases (DZNE) Berlin.
Supplemental data at Neurology.org/nn
- Received April 1, 2017.
- Accepted in final form May 25, 2017.
- Copyright © 2017 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology
This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND), which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
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