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对乙醇代谢产物的免疫反应和细胞因子谱可区分有或无肝脏疾病的酗酒者。

Immune Responses to Ethanol Metabolites and Cytokine Profiles Differentiate Alcoholics with or without Liver Disease.

作者信息

Latvala Jaana, Hietala Johanna, Koivisto Heidi, Järvi Kimmo, Anttila Petra, Niemelä Onni

机构信息

Department of Laboratory Medicine and Addiction Research Unit, EP Central Hospital, Seinäjoki, and University of Tampere, Finland.

出版信息

Am J Gastroenterol. 2005 Jun;100(6):1303-10. doi: 10.1111/j.1572-0241.2005.41509.x.

Abstract

OBJECTIVES

Excessive alcohol consumption is associated with the generation of antibodies against neoantigens induced by ethanol metabolism. However, the associations between such immune responses, ethanol consumption, and liver injury remain unclear.

METHODS

Eight-six male alcoholics with (n=54) or without (n=32) liver disease, and 20 male volunteers (6 abstainers, 14 moderate drinkers) underwent clinical, morphological, and biochemical assessments of liver status and ethanol consumption.

RESULTS

Antiacetaldehyde adduct IgAs in both groups of alcoholics were significantly higher than those in the controls. Elevated IgGs occurred in patients with liver disease, whereas IgMs were high in the heavy drinkers without apparent liver disease. Liver disease patients had high levels of both proinflammatory (IL-2, IL-6, IL-8, TNF-alpha) and antiinflammatory (IL-10) cytokines, whereas those without liver disease showed elevated IL-6, IL-8, and IL-10 only. Ethanol consumption correlated significantly with antiadduct IgA and IL-6 levels, which also showed parallel changes upon abstinence.

CONCLUSIONS

Alcoholic liver disease is associated with the generation of IgAs and IgGs against acetaldehyde-derived antigens and enhanced levels of both pro- and antiinflammatory cytokines, whereas elevated IgA, IL-6, and IL-10 characterize alcoholics without liver disease. These data suggest that immunological mechanisms may play a role in the sequence of events leading to liver disease in some patients with excessive drinking.

摘要

目的

过量饮酒与乙醇代谢诱导产生的新抗原抗体生成有关。然而,这种免疫反应、乙醇摄入与肝损伤之间的关联仍不明确。

方法

86名男性酗酒者(其中54名患有肝病,32名未患肝病)以及20名男性志愿者(6名戒酒者,14名适度饮酒者)接受了肝脏状态和乙醇摄入情况的临床、形态学及生化评估。

结果

两组酗酒者的抗乙醛加合物IgA均显著高于对照组。肝病患者的IgG升高,而无明显肝病的重度饮酒者IgM升高。肝病患者促炎细胞因子(IL-2、IL-6、IL-8、TNF-α)和抗炎细胞因子(IL-10)水平均较高,而无肝病者仅IL-6、IL-8和IL-10升高。乙醇摄入量与抗加合物IgA和IL-6水平显著相关,戒酒时二者也呈现平行变化。

结论

酒精性肝病与针对乙醛衍生抗原的IgA和IgG生成以及促炎和抗炎细胞因子水平升高有关,而无肝病的酗酒者则以IgA、IL-6和IL-10升高为特征。这些数据表明,免疫机制可能在一些过量饮酒患者导致肝病的一系列事件中发挥作用。

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