Effect of tacrolimus on soluble costimulatory molecules in patients with refractory myasthenia gravis

J Neuroimmunol. 2022 Nov 15:372:577955. doi: 10.1016/j.jneuroim.2022.577955. Epub 2022 Aug 27.

Abstract

Objectives: To investigate the expression and possible role of soluble costimulatory molecules in the treatment of refractory myasthenia gravis.

Methods: Thirty-two patients with refractory myasthenia gravis were enrolled into this study and given tacrolimus 3 mg/day. At the beginning of treatment and 12 months follow-up period, clinical data were collected and recorded. The clinical classification of myasthenia gravis Foundation (MGFA) was performed. The MGFA-quantitative myasthenia gravis score (MGFA-QMGS), manual muscle test (MMT), MG activity of daily living (MG-ADL) and the activity of daily living (MG-ADL), the 15-item myasthenia gravis quality of life (MG QOL-15) and the dose change of prednisone were used to evaluate the efficacy. The expression levels of soluble costimulatory molecules and their ligands (sPD-1/sPD-L1, sICOS/sICOSL, sCD40/sCD40L), soluble CD25 and IL-2 in serum were determined by enzyme-linked immunosorbent assay (ELISA).

Results: We observed that oral administration of 3 mg tacrolimus daily for 1 year can significantly improve the clinical symptoms of patients with refractory myasthenia gravis, which is characterized by a significant reduction in clinical scores, such as QMG, MMT, ADL, MGQOL-15, and a reduction daily oral prednisolone (PSL) dose (P < 0.0001).We also found that the levels of plasma sPD-1, sCD40, IL-2 in refractory MG patients increased significantly, and those decreased significantly 12 months after tacrolimus treatment (P < 0.05). The level of sCD25 was negatively correlated with clinical severity scores (P < 0.05). After tacrolimus treatment, the level of sPD-L1 increased although there was no significant difference.

Conclusion: Tacrolimus could relieve the symptoms of refractory MG and significantly decrease the levels of plasma sPD-1, sICOSL, sCD40, sCD25 and IL-2. Soluble costimulatory molecules might be potential biomarkers for MG and tacrolimus treatment.

Keywords: Myasthenia gravis; Prognosis; Refractory myasthenia gravis; Risk factors; Soluble costimulatory molecules; Tacrolimus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Humans
  • Interleukin-2
  • Myasthenia Gravis* / drug therapy
  • Prednisolone / therapeutic use
  • Prednisone / therapeutic use
  • Quality of Life
  • Tacrolimus* / therapeutic use
  • Transcription Factors

Substances

  • Interleukin-2
  • Prednisolone
  • Prednisone
  • Tacrolimus
  • Transcription Factors