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来自丝虫寄生虫诱导IgE的一个因素是人类CD40的激动剂。

A factor of inducing IgE from a filarial parasite is an agonist of human CD40.

作者信息

Imai S, Tezuka H, Furuhashi Y, Muto R, Fujita K

机构信息

Section of Environmental Parasitology, Department of International Health Development, Division of Public Health, Graduate School, Tokyo Medical and Dental University, 1-5-45 Yushima Bunkyo-ku, Tokyo 113-8519.

出版信息

J Biol Chem. 2001 Dec 7;276(49):46118-24. doi: 10.1074/jbc.M104581200. Epub 2001 Oct 8.

Abstract

Immune responses to parasitic helminth are usually characterized by quite mysterious phenomena: dominance of Th2-like immunity and antigen-nonspecific IgE secretion. We previously purified a factor from Dirofilaria immitis that induces antigen-nonspecific IgE in rats and named it DiAg. In the presence of IL-4, DiAg induces mouse B cells to secrete IgE, which is antigen-nonspecific polyclonal antibody. We investigated the biochemical characteristics of DiAg as a factor of inducing IgE in this study. Recombinant DiAg (rDiAg) with interleukin (IL)-4 induced IgE synthesis in highly purified human normal B cells in vitro cell culture systems. The addition of recombinant human soluble CD40 IgG fusion protein (rsCD40-Ig) inhibited induction of IgE synthesis by rDiAg with IL-4. Monocyte cells were stimulated with rDiAg and recombinant human soluble CD40L (rsCD40L); IL-12 and TNF-alpha were induced. The addition of rsCD40-Ig to THP-1 cells activated with rDiAg and rsCD40L inhibited the production of IL-12. rDiAg bound to the monocyte cell membrane fraction and recombinant human soluble CD40; this binding of rDiAg was competitively inhibited by addition of rsCD40L. Moreover, in CD40-deficient mice, IgE production and MLN-B cell proliferation by rDiAg were completely absent. Based on these results, we concluded that DiAg is an agonist of CD40.

摘要

对寄生蠕虫的免疫反应通常具有一些相当神秘的现象

类似Th2免疫的主导地位和抗原非特异性IgE分泌。我们之前从犬恶丝虫中纯化出一种能在大鼠中诱导抗原非特异性IgE的因子,并将其命名为DiAg。在白细胞介素-4(IL-4)存在的情况下,DiAg诱导小鼠B细胞分泌IgE,IgE是一种抗原非特异性多克隆抗体。在本研究中,我们调查了DiAg作为诱导IgE的因子的生化特性。在体外细胞培养系统中,重组DiAg(rDiAg)与白细胞介素(IL)-4可诱导高度纯化的人正常B细胞合成IgE。添加重组人可溶性CD40 IgG融合蛋白(rsCD40-Ig)可抑制rDiAg与IL-4诱导的IgE合成。用rDiAg和重组人可溶性CD40配体(rsCD40L)刺激单核细胞;可诱导产生IL-12和肿瘤坏死因子-α(TNF-α)。向用rDiAg和rsCD40L激活的THP-1细胞中添加rsCD40-Ig可抑制IL-12的产生。rDiAg与单核细胞膜部分和重组人可溶性CD40结合;添加rsCD40L可竞争性抑制rDiAg的这种结合。此外,在CD40缺陷小鼠中,rDiAg完全不会诱导产生IgE,也不会使肠系膜淋巴结B细胞增殖。基于这些结果,我们得出结论:DiAg是CD40的激动剂。

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