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去氧精胍菌素优先抑制抗CD40激活的表面IgD+B淋巴细胞的生长和成熟。

Deoxyspergualin preferentially inhibits the growth and maturation of anti-CD40-activated surface IgD+ B lymphocytes.

作者信息

Morikawa K, Nemoto K, Miyawaki T, Morikawa S

机构信息

Department of Internal Medicine, Shimane Medical University, Japan.

出版信息

Clin Exp Immunol. 1998 Jun;112(3):495-500. doi: 10.1046/j.1365-2249.1998.00602.x.

Abstract

Deoxyspergualin (DSG), an analogue of spermidin, is a potent immunosuppressive drug with an action quite distinct from that of cyclosporin, rapamycin, or FK506. In this study we investigated the effect of DSG and methyldeoxyspergualin (MeDSG) on the proliferation and differentiation of human B cells stimulated with anti-CD40 MoAb. Highly purified B cells obtained from tonsillar samples were used as target cells. Both agents inhibited the proliferative response of anti-CD40-stimulated B cells in the absence and presence of IL-4, IL-2 or IL-10 in a dose-dependent manner. This inhibitory effect differed markedly among cell populations based on surface IgD expression: strong inhibition of sIgD+ B cells but little inhibition of sIgD- B cells. The drugs also suppressed the production of IgG, IgM and IgA by unfractionated B cells, which suggests that DSG acts against post-switch (sIgD-) B cells. Although the drugs suppressed immunoglobulin synthesis by both sIgD+ and sIgD- B cells, the effect was more marked in the sIgD+ B cells. Analysis of the subclass of IgG secreted by sIgD+ B cells revealed a decline in IgG1 and IgG3 in the presence of DSG. These results suggest that DSG preferentially inhibits the growth and maturation of sIgD+ naive B cells.

摘要

去氧精胍菌素(DSG)是亚精胺的类似物,是一种强效免疫抑制药物,其作用与环孢素、雷帕霉素或FK506截然不同。在本研究中,我们调查了DSG和甲基去氧精胍菌素(MeDSG)对用抗CD40单克隆抗体刺激的人B细胞增殖和分化的影响。从扁桃体样本中获得的高度纯化的B细胞用作靶细胞。在有或无白细胞介素-4、白细胞介素-2或白细胞介素-10的情况下,这两种药物均以剂量依赖的方式抑制抗CD40刺激的B细胞的增殖反应。基于表面IgD表达,这种抑制作用在细胞群体之间存在显著差异:对sIgD + B细胞有强烈抑制作用,但对sIgD - B细胞抑制作用很小。这些药物还抑制了未分级B细胞产生IgG、IgM和IgA,这表明DSG作用于转换后(sIgD -)B细胞。尽管这些药物抑制了sIgD +和sIgD - B细胞的免疫球蛋白合成,但对sIgD + B细胞的作用更为明显。对sIgD + B细胞分泌的IgG亚类分析显示,在存在DSG的情况下,IgG1和IgG3减少。这些结果表明,DSG优先抑制sIgD +幼稚B细胞的生长和成熟。

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