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Pathogenic Th17 cells are a potential therapeutic target for tacrolimus in AChR-myasthenia gravis patients.

J Neuroimmunol

November 2024

Department of Neurology, National Key Clinical Department and Key Discipline of Neurology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510080, China. Electronic address:

Article Synopsis
  • The study examined how tacrolimus (TAC) affects CD4+ T cell subsets in 41 patients with AChR-MG over 12 weeks.
  • Results showed that 27 patients responded positively to TAC treatment by exhibiting improved myasthenia gravis scores, while 14 did not respond.
  • The findings suggest that TAC's clinical effectiveness is linked to its ability to lower Th17 and pathogenic Th17 cells, which may improve management of myasthenia gravis by modulating the immune response.
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Background: Myasthenia gravis (MG) is a rare classic autoimmune disease where immunosuppressant therapies have been successful to reduce MG attributable mortality fairly well. However, patients with refractory MG (rMG) among the actively treated MG (aMG) are nonresponsive to conventional therapy and display high disease severity, which calls for further research. We aimed to determine survival, prognosis, and clinical feature of patients with rMG compared to non-rMG.

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