Effect of Fingolimod on Lymphocyte Subsets in Patients With Relapsing Multiple Sclerosis.


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Sarıkaya C., Gacar G., Efendi H.

Cureus, cilt.16, sa.10, 2024 (ESCI) identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 16 Sayı: 10
  • Basım Tarihi: 2024
  • Doi Numarası: 10.7759/cureus.70715
  • Dergi Adı: Cureus
  • Derginin Tarandığı İndeksler: Emerging Sources Citation Index (ESCI)
  • Açık Arşiv Koleksiyonu: AVESİS Açık Erişim Koleksiyonu
  • Kocaeli Üniversitesi Adresli: Evet

Özet

Background and aim

Multiple sclerosis (MS) is the most common chronic inflammatory demyelinating disease of the central

nervous system (CNS). This study aims to evaluate the effect of fingolimod on T and B lymphocytes in

relapsing-remitting multiple sclerosis (RRMS) patients.

Method

Multiple sclerosis patients were selected from patients who were scheduled to start medication at the

outpatient clinic of Kocaeli University, Kocaeli, Turkey, between February 2019 and February 2022. Venous

blood samples were obtained before starting medication from the patients who agreed to participate in the

study and who were to start treatment, simultaneous clinical and neurologic examinations were performed

and the Expanded Disability Status Scale (EDSS) was calculated. After the six-month treatment, venous

blood samples were taken again. Lymphocyte subgroup analyses were performed in the flow cytometry

laboratory.

Results

The study included 48 patients in the fingolimod group and 33 patients as controls. Flow cytometry analyses

showed there was no significant difference between the two groups in the numbers and percentages of

CD19+, CD20+, and CD22+ cells at baseline, while a significant decrease was observed in all of these

parameters in the fingolimod group after the six-month treatment.

Discussion

Our findings support that the fingolimod treatment has significant effects on both lymphocyte counts and

lymphocyte subgroup ratios. The results show the mechanism of action of fingolimod is unaccountable only

through T lymphocytes, and it is effective in both B lymphocyte subgroups and T lymphocytes.