<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Masi G</submitter><funding>National Institute of Allergy and Infectious Diseases</funding><funding>National Institute of Neurological Disorders and Stroke</funding><funding>Takeda Pharmaceuticals U.S.A.</funding><funding>UCB Pharma</funding><funding>NCATS NIH HHS</funding><funding>Genentech</funding><funding>Centers for Disease Control and Prevention</funding><funding>NIAID NIH HHS</funding><funding>NINDS NIH HHS</funding><funding>National Institute of Mental Health</funding><funding>National Institutes of Health</funding><funding>Myasthenia Gravis Foundation of America</funding><pagination>577850</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9106915</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>367</volume><pubmed_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.</pubmed_abstract><journal>Journal of neuroimmunology</journal><pubmed_title>The clinical need for clustered AChR cell-based assay testing of seronegative MG.</pubmed_title><pmcid>PMC9106915</pmcid><funding_grant_id>R01 AI114780</funding_grant_id><funding_grant_id>R21 AI164590</funding_grant_id><funding_grant_id>R01-AI114780</funding_grant_id><funding_grant_id>R21-AI164590</funding_grant_id><funding_grant_id>UL1 TR001863</funding_grant_id><funding_grant_id>U54 NS115054</funding_grant_id><funding_grant_id>T32 AI007019</funding_grant_id><pubmed_authors>Masi G</pubmed_authors><pubmed_authors>Nowak RJ</pubmed_authors><pubmed_authors>O'Connor KC</pubmed_authors><pubmed_authors>Pham MC</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Karatz T</pubmed_authors><pubmed_authors>Oxendine SR</pubmed_authors><pubmed_authors>Guptill JT</pubmed_authors></additional><is_claimable>false</is_claimable><name>The clinical need for clustered AChR cell-based assay testing of seronegative MG.</name><description>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.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jun</publication><modification>2025-04-04T20:20:07.665Z</modification><creation>2025-02-19T02:17:31.268Z</creation></dates><accession>S-EPMC9106915</accession><cross_references><pubmed>35366559</pubmed><doi>10.1016/j.jneuroim.2022.577850</doi></cross_references></HashMap>