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香烟烟雾中的丙烯醛会抑制T细胞反应。

Acrolein in cigarette smoke inhibits T-cell responses.

作者信息

Lambert Cherie, McCue Jesica, Portas Mary, Ouyang Yanli, Li JiMei, Rosano Thomas G, Lazis Alexander, Freed Brian M

机构信息

Division of Allergy and Clinical Immunology, Department of Medicine, University of Colorado at Denver and Health Sciences Center, Denver, CO 80262, USA.

出版信息

J Allergy Clin Immunol. 2005 Oct;116(4):916-22. doi: 10.1016/j.jaci.2005.05.046. Epub 2005 Aug 1.

Abstract

BACKGROUND

Cigarette smoking inhibits T-cell responses in the lungs, but the immunosuppressive compounds have not been fully identified. Cigarette smoke extracts inhibit IL-2, IFN-gamma, and TNF-alpha production in stimulated lymphocytes obtained from peripheral blood, even when the extracts were diluted 100-fold to 1000-fold.

OBJECTIVE

The objective of these studies was to identify the immunosuppressive compounds found in cigarette smoke.

METHODS

Gas chromatography/mass spectroscopy and HPLC were used to identify and quantitate volatile compounds found in cigarette smoke extracts. Bioactivity was measured by viability and production of cytokine mRNA and protein levels in treated human lymphocytes.

RESULTS

The vapor phase of the cigarette smoke extract inhibited cytokine production, indicating that the immunosuppressive compounds were volatile. Among the volatile compounds identified in cigarette smoke extracts, only the alpha,beta-unsaturated aldehydes, acrolein (inhibitory concentration of 50% [IC50] = 3 micromol/L) and crotonaldehyde (IC50 = 6 micromol/L), exhibited significant inhibition of cytokine production. Although the levels of aldehydes varied 10-fold between high-tar (Camel) and ultralow-tar (Carlton) extracts, even ultralow-tar cigarettes produced sufficient levels of acrolein (34 micromol/L) to suppress cytokine production by >95%. We determined that the cigarette smoke extract inhibited transcription of cytokine genes. The inhibitory effects of acrolein could be blocked with the thiol compound N-acetylcysteine.

CONCLUSION

The vapor phase from cigarette smoke extracts potently suppresses cytokine production. The compound responsible for this inhibition appears to be acrolein.

摘要

背景

吸烟会抑制肺部的T细胞反应,但免疫抑制化合物尚未完全明确。香烟烟雾提取物可抑制从外周血获取的受刺激淋巴细胞中白细胞介素-2(IL-2)、干扰素-γ(IFN-γ)和肿瘤坏死因子-α(TNF-α)的产生,即使提取物被稀释100倍至1000倍。

目的

这些研究的目的是鉴定香烟烟雾中存在的免疫抑制化合物。

方法

采用气相色谱/质谱联用技术和高效液相色谱法来鉴定和定量香烟烟雾提取物中的挥发性化合物。通过处理后的人淋巴细胞的活力以及细胞因子mRNA和蛋白质水平的产生来测量生物活性。

结果

香烟烟雾提取物的气相抑制细胞因子的产生,表明免疫抑制化合物是挥发性的。在香烟烟雾提取物中鉴定出的挥发性化合物中,只有α,β-不饱和醛,即丙烯醛(半数抑制浓度[IC50]=3微摩尔/升)和巴豆醛(IC50=6微摩尔/升),对细胞因子的产生有显著抑制作用。尽管高焦油(骆驼牌)和超低焦油(卡尔顿牌)提取物中醛的含量相差10倍,但即使是超低焦油香烟产生的丙烯醛水平(34微摩尔/升)也足以抑制细胞因子产生>95%。我们确定香烟烟雾提取物抑制细胞因子基因的转录。丙烯醛的抑制作用可用硫醇化合物N-乙酰半胱氨酸阻断。

结论

香烟烟雾提取物的气相能有效抑制细胞因子的产生。造成这种抑制作用的化合物似乎是丙烯醛。

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