| Literature DB >> 35366559 |
Gianvito Masi1, Yingkai Li2, Tabitha Karatz2, Minh C Pham3, Seneca R Oxendine1, Richard J Nowak4, Jeffrey T Guptill5, Kevin C O'Connor6.
Abstract
Trial eligibility in myasthenia gravis (MG) remains largely dependent on a positive autoantibody serostatus. This significantly hinders seronegative MG (SNMG) patients from receiving potentially beneficial new treatments. In a subset of SNMG patients, acetylcholine receptor (AChR) autoantibodies are detectable by a clustered AChR cell-based assay (CBA). Of 99 SNMG patients from two academic U.S. centers, 18 (18.2%) tested positive by this assay. Autoantibody positivity was further validated in 17/18 patients. In a complementary experiment, circulating AChR-specific B cells were identified in a CBA-positive SNMG patient. These findings corroborate the clinical need for clustered AChR CBA testing when evaluating SNMG patients.Entities:
Keywords: Autoantibodies; Cell-based assay; Myasthenia gravis; Seronegative
Mesh:
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Year: 2022 PMID: 35366559 PMCID: PMC9106915 DOI: 10.1016/j.jneuroim.2022.577850
Source DB: PubMed Journal: J Neuroimmunol ISSN: 0165-5728 Impact factor: 3.221