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白细胞介素-21对人免疫球蛋白E产生的影响,该影响是针对白细胞介素-4或白细胞介素-13而言的。

IL-21 effects on human IgE production in response to IL-4 or IL-13.

作者信息

Wood Nancy, Bourque Karen, Donaldson Debra D, Collins Mary, Vercelli Donata, Goldman Samuel J, Kasaian Marion T

机构信息

Wyeth Research, Cambridge, MA, USA.

出版信息

Cell Immunol. 2004 Sep-Oct;231(1-2):133-45. doi: 10.1016/j.cellimm.2005.01.001. Epub 2005 Feb 9.

Abstract

In human atopic disease, IgE sensitizes the allergic response, while IgG4 is protective. Because IL-4 and IL-13 trigger switch recombination to both IgE and IgG4, additional agents must regulate the balance between these isotypes to influence susceptibility or tolerance to atopy. In this report, we define in vitro conditions leading to activation or inhibition of human IgE and IgG4 production by IL-21. IL-21 reduced IL-4-driven IgE synthesis by mitogen-stimulated human PBMC. IL-21 inhibition of human IgE production was not a direct effect on B cells, was not seen following B cell activation with IL-13, and was overcome by CD40 ligation. Neither IFN-gamma, IL-10, IL-12, CD40L expression, nor apoptosis was responsible for the inhibitory effect. In contrast, IL-21-stimulated secretion of IgG4 from PBMC. Our findings indicate that IL-21 may influence the production of both human IgE and IgG4, and thus contribute to the regulation of atopic reactions.

摘要

在人类特应性疾病中,IgE使过敏反应致敏,而IgG4具有保护作用。由于白细胞介素-4(IL-4)和白细胞介素-13(IL-13)触发向IgE和IgG4的类别转换重组,因此其他因子必须调节这些同种型之间的平衡,以影响对特应性的易感性或耐受性。在本报告中,我们确定了导致IL-21激活或抑制人IgE和IgG4产生的体外条件。IL-21减少了丝裂原刺激的人外周血单个核细胞(PBMC)中IL-4驱动的IgE合成。IL-21对人IgE产生的抑制作用不是对B细胞的直接作用,在用IL-13激活B细胞后未观察到这种作用,并且通过CD40连接得以克服。γ干扰素(IFN-γ)、IL-10、IL-12、CD40L表达或细胞凋亡均与这种抑制作用无关。相反,IL-21刺激PBMC分泌IgG4。我们的研究结果表明,IL-21可能影响人IgE和IgG4的产生,从而有助于调节特应性反应。

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