Suppr超能文献

人类免疫缺陷病毒gp120抑制人单核细胞分泌白细胞介素-12:一种间接的白细胞介素-10介导的效应。

Human immunodeficiency virus gp120 inhibits interleukin-12 secretion by human monocytes: an indirect interleukin-10-mediated effect.

作者信息

Taoufik Y, Lantz O, Wallon C, Charles A, Dussaix E, Delfraissy J F

机构信息

Laboratoire Virus, Neurones et Immunité, Université Paris-Sud, Le Kremlin-Bicêtre, France.

出版信息

Blood. 1997 Apr 15;89(8):2842-8.

PMID:9108403
Abstract

Interleukin-12 (IL-12), a cytokine with in vitro and in vivo immunomodulatory effects, is produced mostly by activated monocytes and macrophages. To study the effect of human immunodeficiency virus (HIV) infection on IL-12 production, we investigated the expression of IL-12 at mRNA and protein levels by human monocytes preincubated with HIV-gp120. In these conditions, we show that monocytes have a decreased ability to express IL-12 mRNA subunits and to produce IL-12 p40 and bioactive p70 proteins in response to Staphylococcus aureus strain cowan I (SAC). We showed that in human monocyte cultures, HIV-gp120 induces a significant IL-10 synthesis, which in turn inhibits IL-12 subunits mRNA accumulation and protein secretion after SAC-activation. Similar data were obtained with human macrophages. These results suggest that, during HIV infection, gp120 induces in uninfected monocytes and macrophages IL-10/IL-12 disregulation, which can alter immune response.

摘要

白细胞介素-12(IL-12)是一种在体外和体内均具有免疫调节作用的细胞因子,主要由活化的单核细胞和巨噬细胞产生。为了研究人类免疫缺陷病毒(HIV)感染对IL-12产生的影响,我们通过用HIV-gp120预孵育人类单核细胞,在mRNA和蛋白质水平上研究了IL-12的表达。在这些条件下,我们发现单核细胞对金黄色葡萄球菌考恩I株(SAC)作出反应时,表达IL-12 mRNA亚基以及产生IL-12 p40和生物活性p70蛋白的能力下降。我们表明,在人类单核细胞培养物中,HIV-gp120诱导显著的IL-10合成,这反过来又抑制了SAC激活后IL-12亚基mRNA的积累和蛋白质分泌。在人类巨噬细胞中也获得了类似的数据。这些结果表明,在HIV感染期间,gp120在未感染的单核细胞和巨噬细胞中诱导IL-10/IL-12失调,这可能会改变免疫反应。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验