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[活动性多发性硬化症患者淋巴细胞亚群的变化及β-干扰素治疗]

[Changes in lymphocyte subsets s and treatment with beta interferon in active multiple sclerosis].

作者信息

Gata J M, García-Moreno J M, Dinca L, Sánchez-Margalet V, Navarro G, Izquierdo G

机构信息

Servicio de Neurología, Hospital Universitario Virgen de la Macarena, Sevilla, España.

出版信息

Rev Neurol. 1998 Dec;27(160):939-42.

PMID:9951008
Abstract

INTRODUCTION

We report that interferon beta decreases CD8 T cells percentage and increases CD4/CD8 cell's rate in vivo in Multiple Sclerosis (MS) patients.

PATIENTS AND METHODS

We studied 40 patients (22 women and 18 men) with clinically definite active MS who received IFN beta. Twenty-six were treated with nIFN (9 MU/week) and 14 with rIFN (28 MU/week). All patients except two with secondary progressive forms presented relapsing remitting courses. Mean age and mean age at onset were 36.5 +/- 9 and 27.8 +/- 7 years respectively. Mean EDSS score was 2.96 +/- 1.8. Patients were reviewed at four weeks and every eight weeks and periodical studies of immunity were performed. T cell subpopulations (CD3, CD4, CD8 and NK) were studied byflow cytometry.

RESULTS

The evolution of CD8 T cell percentage showed a statistically significant decrease in all blood samples after 20 weeks of treatment with rIFN (24.3 +/- 8 vs 34.7 +/- 5 in the control group) and after 36 weeks for nIFN beta group (25.7 +/- 6 vs 33.0 +/- 4 in the control group). No changes were detected in CD4 T cell subset. The evolution of CD4/CD8 T cell rate showed an increase over the cut-off (2.200) in all blood samples after 20 weeks of treatment with rIFN (2.302 +/- 1.12, 2.332 +/- 0.99 and 2.488 +/- 1.61 for 20, 28 and 36 weeks respectively) and after 52 weeks for nIFN beta group (2.128 +/- 1.07, 2.346 +/- 1.09 and 3.168 +/- 3.87 for 52, 60 and 68 weeks respectively).

CONCLUSIONS

Both nIFN and rIFN beta are able in vivo to decrease CD8 percentage of T cells and increase CD4/CD8+ T cell rate. The increase in the rate is produced earlier in the rIFN treated group.

摘要

引言

我们报告,在多发性硬化症(MS)患者体内,β干扰素可降低CD8 T细胞百分比并提高CD4/CD8细胞比率。

患者与方法

我们研究了40例接受β干扰素治疗的临床确诊活动性MS患者(22名女性和18名男性)。26例接受天然干扰素(nIFN,9 MU/周)治疗,14例接受重组干扰素(rIFN,28 MU/周)治疗。除2例继发进展型患者外,所有患者均呈复发缓解病程。平均年龄和平均发病年龄分别为36.5±9岁和27.8±7岁。平均扩展残疾状态量表(EDSS)评分为2.96±1.8。在4周和每8周时对患者进行复查,并进行定期免疫研究。通过流式细胞术研究T细胞亚群(CD3、CD4、CD8和NK)。

结果

rIFN治疗20周后(对照组为34.7±5,治疗组为24.3±8)以及nIFNβ组治疗36周后(对照组为33.0±4,治疗组为25.7±6),所有血样中CD8 T细胞百分比的变化均显示出统计学上的显著下降。CD4 T细胞亚群未检测到变化。rIFN治疗20周后(20周、28周和36周时分别为2.302±1.12、2.332±0.99和2.488±1.61)以及nIFNβ组治疗52周后(52周、60周和68周时分别为2.128±1.07、2.346±1.09和3.168±3.87),所有血样中CD4/CD8 T细胞比率的变化均显示超过临界值(2.200)升高。

结论

nIFN和rIFNβ在体内均能降低T细胞的CD8百分比并提高CD4/CD8+ T细胞比率。rIFN治疗组比率升高出现得更早。

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