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雷帕霉素和地塞米松对Vogt-小柳原田病患者白细胞介素-17和γ-干扰素产生的抑制作用

Inhibitory effect of rapamycin and dexamethasone on production of IL-17 and IFN-gamma in Vogt-Koyanagi-Harada patients.

作者信息

Yang K, Wen J, Liu X, Kijlstra A, Chen L, Chi W, Zhou H, Huang X, Yang P

机构信息

The First Clinical Hospital of ZhengZhou University, ZhengZhou, PR China.

出版信息

Br J Ophthalmol. 2009 Feb;93(2):249-53. doi: 10.1136/bjo.2008.142489. Epub 2008 Nov 19.

DOI:10.1136/bjo.2008.142489
PMID:19019941
Abstract

AIMS

To evaluate the effect of rapamycin (RAPA) and dexamethasone (DEX) on the production of IL-17 and IFN-gamma by peripheral blood mononuclear cells (PBMCs) from Vogt-Koyanagi-Harada (VKH) patients and healthy individuals.

METHODS

Blood samples were drawn from 10 active VKH patients and 10 healthy individuals. PBMCs were cultured with or without anti-CD3 and anti-CD28 antibodies in the presence or absence of different concentrations of RAPA or DEX for 72 h. IL-17 and IFN-gamma concentrations in the supernatants were measured by enzyme-linked immunosorbent assay (ELISA).

RESULTS

The expression of IL-17 and IFN-gamma was significantly increased in active VKH patients compared with that in healthy controls. Both RAPA and DEX were able to significantly inhibit the production of IL-17 and IFN-gamma by PBMCs from patients and healthy controls. RAPA was able to completely inhibit IL-17 production at a dosage of 10 ng/ml but only partially suppressed IFN-gamma production even at a much higher concentration (1000 ng/ml). DEX inhibited the production of both IL-17 and IFN-gamma by approximately 70%.

CONCLUSIONS

This study indicates that both RAPA and DEX inhibit the production of IL-17 and IFN-gamma by PBMCs. RAPA is much stronger in inhibiting the production of IL-17 than DEX.

摘要

目的

评估雷帕霉素(RAPA)和地塞米松(DEX)对葡萄膜炎-小柳原田病(VKH)患者及健康个体外周血单个核细胞(PBMC)产生白细胞介素-17(IL-17)和干扰素-γ(IFN-γ)的影响。

方法

采集10例活动期VKH患者和10例健康个体的血样。PBMC在有或无抗CD3和抗CD28抗体的情况下,于不同浓度的RAPA或DEX存在或不存在时培养72小时。通过酶联免疫吸附测定(ELISA)测量上清液中IL-17和IFN-γ的浓度。

结果

与健康对照相比,活动期VKH患者中IL-17和IFN-γ的表达显著增加。RAPA和DEX均能显著抑制患者和健康对照的PBMC产生IL-17和IFN-γ。RAPA在剂量为10 ng/ml时能够完全抑制IL-17的产生,但即使在更高浓度(1000 ng/ml)时也只能部分抑制IFN-γ的产生。DEX抑制IL-17和IFN-γ的产生约70%。

结论

本研究表明,RAPA和DEX均抑制PBMC产生IL-17和IFN-γ。RAPA在抑制IL-17产生方面比DEX更强。

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