Research Article

Trail/trail receptor expression on T-cell subtypes in patients with myasthenia gravis

Volume: 42 Number: 3 September 30, 2025
EN

Trail/trail receptor expression on T-cell subtypes in patients with myasthenia gravis

Abstract

Anti- acetylcholine receptor (Anti-AChR) is the most commonly seen and well known antibody among Myasthenia Gravis (MG) related antibodies and it is produced by B lymphocytes; however,,T-lymphocytes also contribute to the development of the autoimmune response. Apoptosis, programmed cell death, regulates the activities of central and peripheral T cells during immune response. In this regard, the goal of this study was to determine T cell related TNF-related apoptosis-inducing ligand (TRAIL) receptor and ligand composition; and TRAIL’s role in the development and progression of the disease in MG patients. Thus, we aimed to understand how TRAIL and its receptors affect T cell function in the pathophysiological mechanism of MG. This study included a total of 25 patients (13 females and 12 males), who were admitted to the department of neurology and diagnosed with MG according to clinical, electrophysiological and laboratory data, and 16 age- and sex-matched healthy volunteers. The expression profile of TRAIL and its receptors on CD3+ CD4+ and CD3+ CD8+ T lymphocytes were investigated with flow cytometry in peripheral blood samples. Furthermore, the relationship between TRAIL/TRAIL receptor expression and clinical findings and , treatment protocol of the patients were analyzed with Spearman’s Rho. It was detected that TRAIL/TRAIL receptor expression on both CD4+ and CD8+ T cells were significantly higher in MG patients compared to control group. In MG patients, while death receptor-4 (DR4) and decoy receptors (DcR), DcR1 and DcR2, were correlated with CD8+ T cells, they were not correlated with CD4+ T cells. In this study, which evaluated TRAIL/TRAIL receptor expression on T cell subtypes in MG patients, we showed that TNF and TRAIL/TRAIL receptor system play a significant role in MG and concluded that these data will contribute to the development of new gene therapies.

Keywords

Supporting Institution

YOK

Ethical Statement

Çukurova Üniversitesi Tıp Fakültesi Girişimsel Olmayan Klinik Araştırmalar Etik kurulu, toplantı sayısı 19, Tarih 2 mayıs 2013, karar no :11

References

  1. Grob D, Brunner N, Namba T, Pagala M. Lifetime course of myasthenia gravis. Muscle Nerve. 2008; 37(2):141-149.
  2. Punga AR, Maddison P, Heckmann JM, Guptill JT, Evoli, A. Epidemiology, diagnostics, and biomarkers of autoimmune neuromuscular junction disorders. The Lancet Neurology, 2022;21(2), 176-188.
  3. Zhang X, Yang M, Xu J, Zhang M, Lang B, Wang W et al. Clinical and serological study of myasthenia gravis in HuBei Province, China. J Neurol Neurosurg Psychiatry. 2007; 78(4):386-390.
  4. Li V, Jasinarachchi M, Butler E. Epidemiology, symptomatology and treatment of patients with myasthenia gravis in an Australian hospital. Intern Med J. 2019; 49(12):1537-1540.
  5. Mantegazza R, Cavalcante P. Diagnosis and treatment of myasthenia gravis. Curr Opin Rheumatol. 2019; 31(6):623-33.
  6. Carding SR, Egan PJ. Gammadelta T cells: functional plasticity and heterogeneity. Nat Rev Immunol. 2002; 2(5):336-345.
  7. Godfrey DI, Berzins SP. Control points in NKT-cell development. Nat Rev Immunol. 2007; 7(7): 505-518.
  8. Niu L, Jiang J, Yin Y, Hu B. LncRNA XLOC_003810 modulates thymic Th17/Treg balance in myasthenia gravis with thymoma. Clin Exp Pharmacol Physiol. 2020 Feb 11. doi: 10.1111/1440-1681.13280.

Details

Primary Language

English

Subjects

Neurology and Neuromuscular Diseases

Journal Section

Research Article

Publication Date

September 30, 2025

Submission Date

January 20, 2025

Acceptance Date

July 2, 2025

Published in Issue

Year 2025 Volume: 42 Number: 3

APA
Dincer, A., İşcan, D., Bişgin, A., & Koç, F. (2025). Trail/trail receptor expression on T-cell subtypes in patients with myasthenia gravis. Deneysel Ve Klinik Tıp Dergisi, 42(3), 257-265. https://izlik.org/JA95AN23TJ
AMA
1.Dincer A, İşcan D, Bişgin A, Koç F. Trail/trail receptor expression on T-cell subtypes in patients with myasthenia gravis. J. Exp. Clin. Med. 2025;42(3):257-265. https://izlik.org/JA95AN23TJ
Chicago
Dincer, Ali, Dilek İşcan, Atıl Bişgin, and Filiz Koç. 2025. “Trail/Trail/Receptor/Expression/on/T-Cell/Subtypes/in/Patients/With/Myasthenia/Gravis”. Deneysel Ve Klinik Tıp Dergisi 42 (3): 257-65. https://izlik.org/JA95AN23TJ.
EndNote
Dincer A, İşcan D, Bişgin A, Koç F (September 1, 2025) Trail/trail receptor expression on T-cell subtypes in patients with myasthenia gravis. Deneysel ve Klinik Tıp Dergisi 42 3 257–265.
IEEE
[1]A. Dincer, D. İşcan, A. Bişgin, and F. Koç, “Trail/trail receptor expression on T-cell subtypes in patients with myasthenia gravis”, J. Exp. Clin. Med., vol. 42, no. 3, pp. 257–265, Sept. 2025, [Online]. Available: https://izlik.org/JA95AN23TJ
ISNAD
Dincer, Ali - İşcan, Dilek - Bişgin, Atıl - Koç, Filiz. “Trail/Trail/Receptor/Expression/on/T-Cell/Subtypes/in/Patients/With/Myasthenia/Gravis”. Deneysel ve Klinik Tıp Dergisi 42/3 (September 1, 2025): 257-265. https://izlik.org/JA95AN23TJ.
JAMA
1.Dincer A, İşcan D, Bişgin A, Koç F. Trail/trail receptor expression on T-cell subtypes in patients with myasthenia gravis. J. Exp. Clin. Med. 2025;42:257–265.
MLA
Dincer, Ali, et al. “Trail/Trail/Receptor/Expression/on/T-Cell/Subtypes/in/Patients/With/Myasthenia/Gravis”. Deneysel Ve Klinik Tıp Dergisi, vol. 42, no. 3, Sept. 2025, pp. 257-65, https://izlik.org/JA95AN23TJ.
Vancouver
1.Ali Dincer, Dilek İşcan, Atıl Bişgin, Filiz Koç. Trail/trail receptor expression on T-cell subtypes in patients with myasthenia gravis. J. Exp. Clin. Med. [Internet]. 2025 Sep. 1;42(3):257-65. Available from: https://izlik.org/JA95AN23TJ