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评估布地奈德对从哮喘患者分离出的血液单核细胞的丝裂原诱导或变应原诱导激活的抑制作用。

Evaluation of the inhibitory effects of budesonide on the mitogen-induced or the allergen-induced activation of blood mononuclear cells isolated from asthmatic patients.

作者信息

Oddera S, Silvestri M, Sacco O, Lantero S, Morelli M C, Rossi G A

机构信息

Division of Pneumology, G. Gaslini Institute, Genoa, Italy.

出版信息

Ann Allergy Asthma Immunol. 1995 Jul;75(1):33-40.

PMID:7621058
Abstract

BACKGROUND

Corticosteroids are thought to be effective in the treatment of allergic reactions including bronchial asthma because they not only have anti-inflammatory effects, but also downregulate the processes of T-cell activation.

OBJECTIVE

To evaluate in vitro the inhibitory activity of budesonide, a widely used inhaled corticosteroid, on allergen-induced mononuclear cell activation.

METHODS

Thirty-one atopic asthmatic patients, sensitized to Dermatophagoides pteronyssinus (Der p) were studied. Peripheral blood mononuclear cells isolated from these patients were used to determine the ability of budesonide to inhibit (1) the proliferative response of blood T-lymphocytes to Der p allergen extract and to phytohemoagglutinin (PHA) and (2) the release of different cytokines known to modulate the interaction between T-lymphocytes and monocytes in the allergic processes.

RESULTS

A significant T-cell proliferation was observed both in the presence of PHA (P < .001) and that of Der p allergen extract (P < .05), and was associated with increased release of interleukin-2 [IL-2 (respectively P < .001 and P < .01)], gamma-interferon [gamma-IFN (respectively P < .001 and P < .01)], granulocyte-macrophage colony-stimulating factor [GM-CSF (respectively P < .01 and P < .001)], interleukin-1 beta [IL-1 beta (respectively P < .05 and P < .01)], and tumor necrosis factor-alpha [TNF-alpha (P < .05 each comparison)]. The addition at the beginning of the cell cultures of different concentrations (from 10(-10) M to 10(-7) M) of budesonide, and as control of dexamethasone, induced a dose-dependent inhibition of T-cell proliferation, in response to PHA and Der p. Budesonide at the lowest concentrations tested (10(-10) M and 10(-9) M) was more effective than dexamethasone. Budesonide was also more active than dexamethasone in inhibiting the release of IL-2, gamma-IFN, IL-1 beta and GM-CSF (in both PHA-stimulated and Der p-stimulated blood mononuclear cell cultures) and TNF-alpha (in Der p-stimulated blood mononuclear cell cultures).

CONCLUSIONS

Budesonide is equally or more effective than dexamethasone in inhibiting the allergen-induced T-cell proliferation and in reducing the release of cytokines by allergen-stimulated blood mononuclear cells.

摘要

背景

皮质类固醇被认为对包括支气管哮喘在内的过敏反应有效,因为它们不仅具有抗炎作用,还能下调T细胞活化过程。

目的

在体外评估广泛使用的吸入性皮质类固醇布地奈德对变应原诱导的单核细胞活化的抑制活性。

方法

研究了31名对尘螨(Der p)致敏的特应性哮喘患者。从这些患者中分离出外周血单核细胞,以确定布地奈德抑制(1)血液T淋巴细胞对Der p变应原提取物和植物血凝素(PHA)的增殖反应,以及(2)在过敏过程中已知调节T淋巴细胞与单核细胞相互作用的不同细胞因子释放的能力。

结果

在存在PHA(P <.001)和Der p变应原提取物(P <.05)的情况下均观察到显著的T细胞增殖,并且与白细胞介素-2 [IL-2(分别为P <.001和P <. ,01)]、γ-干扰素[γ-IFN(分别为P <.001和P <.01)]、粒细胞-巨噬细胞集落刺激因子[GM-CSF(分别为P <.01和P <.001)]、白细胞介素-1β[IL-1β(分别为P <.05和P <.01)]和肿瘤坏死因子-α [TNF-α(每次比较P <.05)]释放增加有关。在细胞培养开始时加入不同浓度(从10^(-10) M到10^(-7) M)的布地奈德,并作为地塞米松的对照,可诱导对PHA和Der p的T细胞增殖的剂量依赖性抑制。在测试的最低浓度(10^(-10) M和10^(-9) M)下,布地奈德比地塞米松更有效。在抑制IL-2、γ-IFN、IL-1β和GM-CSF的释放(在PHA刺激和Der p刺激的血液单核细胞培养物中)以及TNF-α(在Der p刺激的血液单核细胞培养物中)方面,布地奈德也比地塞米松更具活性。

结论

在抑制变应原诱导的T细胞增殖以及减少变应原刺激的血液单核细胞释放细胞因子方面,布地奈德与地塞米松同样有效或更有效。

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