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    <responseDate>2026-10-12T04:44:51Z</responseDate>
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    <identifier>10.57760/sciencedb.33610</identifier>
    <datestamp>2026-01-08T17:33:46Z</datestamp>
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  <dc:date>2026-01-08</dc:date>
  <dc:title>Application Analysis of Transfected Cell Method for Detecting AChR Antibodies in MG Patients</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.33610</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>Objective:&amp;nbsp;This study aimed to establish a technical process for detecting nicotinic acetylcholine receptor (nAChR) antibodies using the transfected cell method and evaluate its application in the serological diagnosis of myasthenia gravis (MG) , thereby enhancing&amp;nbsp;diagnostic efficiency.Methods:&amp;nbsp;Cell transfection technology was used&amp;nbsp;to introduce various nAChR&amp;nbsp;subunit combinations into HEK293 cells for antibody detection. Indirect immunofluorescence (IIF) was utilized&amp;nbsp;to test nAChR&amp;nbsp;antibodies in serum samples from 85 MG patients, and the results were compared for consistency with those of enzyme-linked immunosorbent assay (ELISA).Results:&amp;nbsp;The combination of fetal and adult AChR&amp;nbsp;subunits in transfected cells exhibited&amp;nbsp;the highest sensitivity for detecting serum antibodies&amp;nbsp;in patients with MG. The prepared cell slides demonstrated excellent consistency with the ELISA kit results for 85 MG patients, yielding&amp;nbsp;a Kappa value of 0.769, indicating excellent agreement between the two methods.Conclusion:&amp;nbsp;Co-transfection of multiple AChR&amp;nbsp;subunits successfully generated&amp;nbsp;a cell expressing clustered nAChRs, establishing a highly sensitive detection technique for nAChR&amp;nbsp;antibodies. This technique&amp;nbsp;is invaluable&amp;nbsp;for serological detection of patients with MG, facilitating&amp;nbsp;early disease detection, condition assessment, and therapeutic guidance.</dc:description>
  <dc:subject>Acetylcholine Receptor(AChR); Autoantibody; Myasthenia Gravis(MG); Ptosis; Transfected Cell; Indirect Immunofluorescence (IIF) Data Access Statement: Data supporting the findings of this study are available upon reasonable request to the corresponding author.</dc:subject>
  <dc:creator>liu wei</dc:creator>
  <dc:rights>EMBARGO</dc:rights>
  <dc:rights>https://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:publisher>Science Data Bank</dc:publisher>
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