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早期前浆细胞定义了自身反应性B细胞的一个耐受性检查点。

Early preplasma cells define a tolerance checkpoint for autoreactive B cells.

作者信息

Culton Donna A, O'Conner Brian P, Conway Kara L, Diz Ramiro, Rutan Jennifer, Vilen Barbara J, Clarke Stephen H

机构信息

Department of Microbiology and Immunology, University of North Carolina, Chapel Hill, NC 27599, USA.

出版信息

J Immunol. 2006 Jan 15;176(2):790-802. doi: 10.4049/jimmunol.176.2.790.

Abstract

Ab-secreting plasma cells (PCs) are the effectors of humoral immunity. In this study, we describe regulation of autoreactive B cells specific for the ribonucleoprotein Smith (Sm) at an early pre-PC stage. These cells are defined by the expression of the PC marker CD138 and normal levels of CD19 and B220. They are present at a high frequency in normal mouse spleen and bone marrow, are Ag dependent, and are located predominantly along the T cell-B cell border and near bridging channels. Anti-Sm pre-PCs also occur at a high frequency in nonautoimmune mice and show additional phenotypic characteristics of PC differentiation. However, while some of these pre-PCs are Ab-secreting cells, those specific for Sm are not, indicating regulation. Consistent with this, anti-Sm pre-PCs have a higher turnover rate and higher frequency of cell death than those that do not bind Sm. Regulation of anti-Sm pre-PCs occurs upstream of the transcriptional repressor, B lymphocyte-induced maturation protein-1, expression. Regulation at this stage is overcome in autoimmune MRL/lpr mice and is accompanied by an altered B lymphocyte stimulator receptor profile. These data reveal a new B cell tolerance checkpoint that is overcome in autoimmunity.

摘要

分泌抗体的浆细胞(PCs)是体液免疫的效应细胞。在本研究中,我们描述了在早期前浆细胞阶段对核糖核蛋白史密斯(Sm)具有特异性的自身反应性B细胞的调控。这些细胞由浆细胞标志物CD138以及正常水平的CD19和B220的表达来定义。它们在正常小鼠脾脏和骨髓中以高频率存在,依赖抗原,并且主要位于T细胞 - B细胞边界以及桥接通道附近。抗Sm前浆细胞在非自身免疫小鼠中也以高频率出现,并表现出浆细胞分化的其他表型特征。然而,虽然这些前浆细胞中的一些是分泌抗体的细胞,但那些对Sm具有特异性的细胞则不是,这表明存在调控。与此一致的是,抗Sm前浆细胞比那些不结合Sm的前浆细胞具有更高的更新率和更高的细胞死亡频率。抗Sm前浆细胞的调控发生在转录抑制因子B淋巴细胞诱导成熟蛋白-1表达的上游。在自身免疫性MRL/lpr小鼠中,这一阶段的调控被克服,并伴随着B淋巴细胞刺激因子受体谱的改变。这些数据揭示了一种在自身免疫中被克服的新的B细胞耐受性检查点。

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