In:
Annals of the New York Academy of Sciences, Wiley, Vol. 1412, No. 1 ( 2018-01), p. 90-94
Abstract:
Patients with myasthenia gravis (MG) without antibodies to the acetylcholine receptor (AChR) or muscle‐specific tyrosine kinase (MuSK) have been classified as having double‐seronegative myasthenia gravis (dSNMG). We used the sera from six dSNMG patients with positive immunohistochemistry assays in a protein array to screen reactivity with 9000 human proteins. We identified cortactin, an intracellular protein that interacts with agrin/MuSK favoring AChR aggregation, as a new antigen in dSNMG. We then designed an in‐house enzyme‐linked immunosorbent assay as a screening assay and confirmed these results by western blot. We found that 19.7% of dSNMG patients had anti‐cortactin antibodies. In contrast, patients with AChR + MG or other autoimmune disorders and healthy controls were positive at significantly lower rates. Five percent of healthy controls were positive. In a recent study, we screened sera from 250 patients (AChR + MG, MuSK + MG, dSNMG) and 29 healthy controls. Cortactin antibodies were identified in 23.7% of dSNMG and 9.5% AChR + MG patients ( P = 0.02). None of the MuSK + MG patients, patients with other autoimmune disorders, or healthy controls had antibodies against cortactin. Patients with dSNMG cortactin + MG were negative for anti‐striated muscle and anti‐LRP4 antibodies. Patients with dSNMG cortactin + MG presented ocular or mild generalized MG without bulbar symptoms. We conclude that cortactin autoantibodies are biomarkers of MG that, when present, suggest that the disease will be mild.
Type of Medium:
Online Resource
ISSN:
0077-8923
,
1749-6632
DOI:
10.1111/nyas.2018.1412.issue-1
Language:
English
Publisher:
Wiley
Publication Date:
2018
detail.hit.zdb_id:
2834079-6
detail.hit.zdb_id:
211003-9
detail.hit.zdb_id:
2071584-5
SSG:
11
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