芬戈莫德对MS患者白细胞、淋巴细胞和中性粒细胞计数的影响。

IF 1.4 Q4 IMMUNOLOGY American journal of clinical and experimental immunology Pub Date : 2019-04-15 eCollection Date: 2019-01-01
Aryan Rafiee Zadeh, Sara Parsa, Nooshin Tavoosi, Mohsen Farshi, Mohammad Farid Masaeli
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引用次数: 0

摘要

芬戈莫德是一种用于治疗复发-缓解型多发性硬化症(RRMS)的免疫调节口服药物。其预防复发的确切机制尚不清楚。此外,它对免疫细胞群的影响仍未确定。目的:本研究将测量MS患者治疗一个月后白细胞、淋巴细胞和中性粒细胞细胞群的变化。方法:选取伊斯法罕省伴有RRMS的多发性硬化症患者66例,根据一定的排除标准和口服芬戈莫德治疗的资格。获得了白细胞、淋巴细胞和中性粒细胞群体的初始细胞计数。然后在医生的监督下开始每日服用芬戈莫德0.5毫克。治疗1个月后,重复细胞计数。采用SPSS进行统计分析。结果:在该患者队列中,淋巴细胞和白细胞平均细胞计数均显著降低。在这66例患者队列中,中性粒细胞平均细胞计数显著增加。只有白细胞数量的减少在男性和女性人群中都是显著的。只有女性亚群的中性粒细胞和淋巴细胞有显著变化,分别增加和减少。男性亚队列保持相同的方向性,但没有产生统计学意义。结论:虽然在大多数患者群体中,芬戈莫德已被证明可以有效地减少淋巴细胞,但其对中性粒细胞的影响尚未得到大量研究。此外,对芬戈莫德治疗的淋巴细胞和中性粒细胞的反应可能存在性别差异,这表明男性和女性在RRMS发病机制上可能存在差异。
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Effect of fingolimod on white blood cell, lymphocyte and neutrophil counts in MS patients.

Introduction: Fingolimod is an immunomodulating oral treatment used for treating relapsing-remitting multiple sclerosis (RRMS). The exact mechanism for its action in preventing relapses is unknown. Also, its affect on immune cell populations remains unestablished.

Objectives: This study will measure the changes in cell populations of WBCs, lymphocytes, and neutrophils in MS patients after one month of treatment.

Methods: 66 MS patients from Isfahan Province with RRMS were chosen based on certain exclusion criteria and eligibility for fingolimod oral treatment. Initial cell counts for WBC, lymphocyte, and neutrophil cell populations were achieved. Fingolimod .5 mg daily treatment was then initiated under the supervision of a physician. After one month of treatment, cell counts were repeated. Statistical analysis was performed using SPSS.

Results: Both lymphocyte and WBC mean cell counts were significantly decreased in this patient cohort. Neutrophil average cell counts were significantly increased in this 66 patient cohort. Only the decrease of WBC populations was significant for both male and female cohorts individually. Only female sub-cohorts were significantly changed for neutrophils and lymphocytes, increased and decreased respectively. Male sub-cohorts maintained the same directionality but failed to produce statistical significance.

Conclusion: While fingolimod has been effectively proven as reducing lymphocyte cells in most patient populations, its effects on neutrophils have not been studied in abundance. Also, there may be sex-related differences in responses to fingolimod treatment with regards to lymphocytes and neutrophils, suggesting a possible difference in RRMS pathogenesis between males and females.

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