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[糖皮质激素对系统性红斑狼疮患者Th细胞因子平衡的影响]

[Effect of corticosteroids on the balance of Th cytokines in patients with systemic lupus erythematosus].

作者信息

Xie Hong-fu, Li Jie, Shi Wei

机构信息

Department of Dermatology, Xiangya Hospital, Central South University, Changsha 410008, China.

出版信息

Hunan Yi Ke Da Xue Xue Bao. 2002 Dec 28;27(6):533-5.

Abstract

OBJECTIVE

To investigate the levels of Th cell-derived cytokines and the effect of corticosteroids on the balance of Th1/Th2 cytokines in patients with systemic lupus erythematosus (SLE).

METHODS

Fifty-eight SLE patients were treated with corticosteroids. Their IFN-gamma, IL-4 and IL-10 levels were detected by ELISA before and after the treatment with corticosteroids respectively; and the SLEDAI scores of the patients were compared before and after the treatment.

RESULTS

Before the treatment, the serum levels of IFN-gamma, IL-4 and IL-10 were higher than those of the healthy controls (P < 0.05). After the treatment with corticosteroids, the elevated levels of IFN-gamma, IL-4 and IL-10 in the SLE patients were all significantly reduced than those before the treatment (P < 0.05). At the same time, the SLEDAI scores were significantly lower than those before the treatment (P < 0.01). The serum level of IFN-gamma was significantly decreased in the patients with SLE compared with the healthy controls (P < 0.05). By contrast, the levels of IL-4 and IL-10 of the patients with SLE were significantly increased compared with the healthy controls (P < 0.05).

CONCLUSION

Corticosteroids may induce a shift from the Th1 to Th2 profile of cytokine secretion. This may be one aspect of the mechanisms for corticosteroids treatment.

摘要

目的

探讨系统性红斑狼疮(SLE)患者Th细胞衍生细胞因子水平及皮质类固醇对Th1/Th2细胞因子平衡的影响。

方法

58例SLE患者接受皮质类固醇治疗。分别用ELISA法检测其在皮质类固醇治疗前后的IFN-γ、IL-4和IL-10水平;比较患者治疗前后的SLEDAI评分。

结果

治疗前,SLE患者血清IFN-γ、IL-4和IL-10水平高于健康对照(P<0.05)。皮质类固醇治疗后,SLE患者升高的IFN-γ、IL-4和IL-10水平均较治疗前显著降低(P<0.05)。同时,SLEDAI评分显著低于治疗前(P<0.01)。SLE患者血清IFN-γ水平较健康对照显著降低(P<0.05)。相比之下,SLE患者IL-4和IL-10水平较健康对照显著升高(P<0.05)。

结论

皮质类固醇可能诱导细胞因子分泌从Th1型向Th2型转变。这可能是皮质类固醇治疗机制的一个方面。

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