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重组人促红细胞生成素对体外人IgE产生的影响。

Effect of recombinant human erythropoietin on human IgE production in vitro.

作者信息

Kimata H, Yoshida A, Ishioka C, Mikawa H

机构信息

Department of Paediatrics, Kyoto University Hospital, Japan.

出版信息

Clin Exp Immunol. 1991 Mar;83(3):483-7. doi: 10.1111/j.1365-2249.1991.tb05665.x.

DOI:10.1111/j.1365-2249.1991.tb05665.x
PMID:2004487
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1535330/
Abstract

Recombinant human erythropoietin enhanced spontaneous IgE production (200-300% enhancement) in cultures of peripheral blood mononuclear cells (MNC) from atopic patients. In contrast, IgG and IgA production were only slightly enhanced (30-50% enhancement), and IgM production was not affected by erythropoietin. The enhancement of IgE production by erythropoietin was indirect since it required T cells and monocytes. However, erythropoietin effect was specific since enhancement was blocked by anti-erythropoietin antibody but not by control antibody. Interleukin-4 (IL-4) also enhanced spontaneous IgE production from atopic MNC. However, the enhancing effect by erythropoietin is different from that by IL-4, since the erythropoietin effect was not blocked by anti-IL-4 antibody, and conversely IL-4 effect was not blocked by anti-erythropoietin antibody. In contrast to the enhancing effect on atopic MNC, erythropoietin failed to induce IgE production in cultures of MNC from normal donors while IL-4 induced IgE production from normal MNC. However, when normal MNC were pre-incubated with IL-4, erythropoietin enhanced IgE production from IL-4-pre-incubated MNC. Moreover, B cells separated from IL-4-pre-incubated MNC produced IgE which was enhanced by erythropoietin. However, this effect required T cells and monocytes. These results indicate that erythropoietin could regulate ongoing IgE production in vitro by T cell- and monocyte-dependent mechanisms.

摘要

重组人促红细胞生成素可增强特应性患者外周血单个核细胞(MNC)培养物中自发性IgE的产生(增强200 - 300%)。相比之下,IgG和IgA的产生仅略有增强(增强30 - 50%),而IgM的产生不受促红细胞生成素的影响。促红细胞生成素对IgE产生的增强作用是间接的,因为它需要T细胞和单核细胞。然而,促红细胞生成素的作用具有特异性,因为其增强作用被抗促红细胞生成素抗体阻断,而未被对照抗体阻断。白细胞介素-4(IL-4)也可增强特应性MNC自发性IgE的产生。然而,促红细胞生成素的增强作用与IL-4不同,因为促红细胞生成素的作用未被抗IL-4抗体阻断,反之,IL-4的作用也未被抗促红细胞生成素抗体阻断。与对特应性MNC的增强作用相反,促红细胞生成素未能在正常供体的MNC培养物中诱导IgE产生,而IL-4可诱导正常MNC产生IgE。然而,当正常MNC与IL-4预孵育后,促红细胞生成素可增强来自IL-4预孵育MNC的IgE产生。此外,从IL-4预孵育MNC中分离出的B细胞产生的IgE可被促红细胞生成素增强。然而,这种作用需要T细胞和单核细胞。这些结果表明,促红细胞生成素可通过T细胞和单核细胞依赖的机制在体外调节正在进行的IgE产生。

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IgE production by normal human lymphocytes is induced by interleukin 4 and suppressed by interferons gamma and alpha and prostaglandin E2.正常人淋巴细胞产生的IgE由白细胞介素4诱导,而被γ干扰素、α干扰素和前列腺素E2抑制。
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IL-4 is an essential factor for the IgE synthesis induced in vitro by human T cell clones and their supernatants.白细胞介素-4是人类T细胞克隆及其上清液在体外诱导产生免疫球蛋白E合成的关键因素。
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Human recombinant interleukin 4 induces Fc epsilon receptors (CD23) on normal human B lymphocytes.人重组白细胞介素4可诱导正常人B淋巴细胞上的Fcε受体(CD23)。
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