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甲泼尼龙可预防肿瘤坏死因子-α依赖性多核巨细胞形成。

Methylprednisolone prevents tumour necrosis factor-alpha-dependent multinucleated giant cell formation.

机构信息

Institute for Inflammation Research, Department of Rheumatology, Rigshospitalet, The University Hospital of Copenhagen, Copenhagen, Denmark.

出版信息

Rheumatology (Oxford). 2010 Nov;49(11):2037-42. doi: 10.1093/rheumatology/keq213. Epub 2010 Jul 15.

Abstract

OBJECTIVES

Granulomas contain multinucleated giant cells (MGCs), the function of which remains largely unknown. In patients with autoimmune granulomatous disease, the granulomas can be resolved during treatment with glucocorticosteroid (GCS). However, little is known about the influence of GCSs on the formation of MGCs.

METHODS

Monocytes isolated from buffy coats were stimulated with IFN-γ and Concanavalin A to form MGCs either in presence or absence of TNF-α, methylprednisolone (MP), adalimumab or human immunoglobulin G. The concentrations of IL-1β, IL-6, IL-10, IL-12p70 and TNF-α in the culture supernatants were measured after 18 h of stimulation.

RESULTS

MP, at a concentration of 0.1 µM, inhibited monocyte fusion (P < 0.05), and abrogated the formation of MGCs completely at higher concentrations. The production of IL-1β, IL-6 and TNF-α that accompanied MGC formation was reduced significantly by 10 µM MP. Recombinant TNF-α, at a concentration of 50 ng/ml, increased the number of formed MGCs and counteracted the inhibitory effect of 0.1 µM MP, while higher concentrations of MP still blocked MGC formation completely. Blockade of TNF-α with adalimumab within 16 h after stimulation significantly reduced the number MGCs formed (P < 0.05).

CONCLUSION

MP inhibits the fusion of monocytes into MGCs, as well as the monocyte production of pro-inflammatory cytokines, which may be an important aspect of its beneficial effect in chronic granulomatous disorders. MCG formation can be promoted by TNF-α and inhibited by TNF-α blockade.

摘要

目的

肉芽肿中含有多核巨细胞(MGC),但其功能仍知之甚少。在自身免疫性肉芽肿疾病患者中,糖皮质激素(GCS)治疗可使肉芽肿消退。然而,关于 GCS 对 MGC 形成的影响知之甚少。

方法

从白细胞中分离出单核细胞,用 IFN-γ 和刀豆蛋白 A 刺激形成 MGC,在有或没有 TNF-α、甲泼尼龙(MP)、阿达木单抗或人免疫球蛋白 G 的情况下进行刺激。刺激 18 小时后,测量培养上清液中 IL-1β、IL-6、IL-10、IL-12p70 和 TNF-α 的浓度。

结果

MP 浓度为 0.1 μM 时抑制单核细胞融合(P < 0.05),在更高浓度时完全阻断 MGC 的形成。与 MGC 形成伴随的 IL-1β、IL-6 和 TNF-α 的产生,被 10 μM MP 显著减少。浓度为 50 ng/ml 的重组 TNF-α增加了形成的 MGC 数量,并抵消了 0.1 μM MP 的抑制作用,而更高浓度的 MP 仍完全阻断 MGC 的形成。刺激后 16 小时内用阿达木单抗阻断 TNF-α可显著减少形成的 MGC 数量(P < 0.05)。

结论

MP 抑制单核细胞融合为 MGC,以及单核细胞产生促炎细胞因子,这可能是其在慢性肉芽肿性疾病中有益作用的一个重要方面。TNF-α 可促进 MCG 形成,而 TNF-α 阻断可抑制 MCG 形成。

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