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白细胞介素-12可短暂诱导人CD4 +过敏原特异性Th2 T细胞克隆中的γ干扰素转录和蛋白质合成。

IL-12 transiently induces IFN-gamma transcription and protein synthesis in human CD4+ allergen-specific Th2 T cell clones.

作者信息

Yssel H, Fasler S, de Vries J E, de Waal Malefyt R

机构信息

DNAX Research Institute for Molecular and Cellular Biology, Human Immunology Department, Palo Alto, CA 94304-1104.

出版信息

Int Immunol. 1994 Jul;6(7):1091-6. doi: 10.1093/intimm/6.7.1091.

Abstract

IL-12 is a cytokine produced by monocytes and Epstein-Barr virus-transformed B cells which initiates Th1 responses by inducing the development of CD4+, IFN-gamma producing Th1 T cells in mouse and human. We have previously reported that allergen-specific CD4+ Th2 T cell clones produce IFN-gamma, following activation by phorbol ester (TPA) and calcium ionophore, indicating that these cells still have the ability to produce IFN-gamma. This observation, together with the capacity of IL-12 to induce IFN-gamma, prompted us to examine the effects of rIL-12 on the cytokine production profiles of a panel of cloned allergen-specific Th2 cell lines, and compare these to the effects of rIL-12 on the cytokine production by Th0 and Th1 T cell clones. Activation with antigen or TPA/anti-CD3 mAb of Th2 T cell clones that had been preincubated with rIL-12 and rIL-2 for 5 days induced or enhanced the expression of IFN-gamma transcripts, as well as the production of IFN-gamma by these cells. Furthermore, in a different set of experiments, it was found that the presence of rIL-12 during a 12 h stimulation of Th2 T cell clones induced or enhanced the expression of IFN-gamma transcripts, as well as the production of IFN-gamma by these cells. rIL-12 also enhanced IFN-gamma production by Th0 and Th1 T cells, but, in contrast, rIL-12 had no effect on the production of IL-4, nor on the frequency of IL-4 producing cells, as judged by analysis of intracellularly produced cytokines.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

白细胞介素-12是一种由单核细胞和爱泼斯坦-巴尔病毒转化的B细胞产生的细胞因子,它通过诱导小鼠和人类中产生干扰素-γ的CD4+ Th1 T细胞的发育来启动Th1反应。我们之前报道过,变应原特异性CD4+ Th2 T细胞克隆在佛波酯(TPA)和钙离子载体激活后会产生干扰素-γ,这表明这些细胞仍有产生干扰素-γ的能力。这一观察结果,连同白细胞介素-12诱导干扰素-γ的能力,促使我们研究重组白细胞介素-12(rIL-12)对一组克隆的变应原特异性Th2细胞系细胞因子产生谱的影响,并将其与rIL-12对Th0和Th1 T细胞克隆细胞因子产生的影响进行比较。用抗原或TPA/抗CD3单克隆抗体激活预先用rIL-12和rIL-2孵育5天的Th2 T细胞克隆,可诱导或增强这些细胞中干扰素-γ转录本的表达以及干扰素-γ的产生。此外,在另一组实验中发现,在对Th2 T细胞克隆进行12小时刺激期间存在rIL-12,可诱导或增强这些细胞中干扰素-γ转录本的表达以及干扰素-γ的产生。rIL-12还增强了Th0和Th1 T细胞产生干扰素-γ的能力,但相比之下,通过对细胞内产生的细胞因子进行分析判断,rIL-12对白细胞介素-4的产生以及产生白细胞介素-4的细胞频率没有影响。(摘要截短于250字)

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