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首页> 外文期刊>The journal of immunology >L Chain Allelic Inclusion Does Not Increase Autoreactivity in Lupus-Prone New Zealand Black/New Zealand White Mice
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L Chain Allelic Inclusion Does Not Increase Autoreactivity in Lupus-Prone New Zealand Black/New Zealand White Mice

机译:L链等位基因包涵不增加狼疮新西兰黑/新西兰白小鼠的自身反应性

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L chain allelic inclusion has been proposed as a B cell tolerance mechanism in addition to clonal deletion, clonal anergy, and receptor editing. It is said to rescue autoreactive B cells from elimination by diluting out the self-reactive BCR through the expression of a second innocuous L chain. In autoimmune animals, such as lupus-prone mice, allelically included B cells could be activated and produce pathogenic autoantibodies. We have previously shown that anti-DNA hybridomas from diseased New Zealand Black/New Zealand White F1 mice exhibit nearly perfect allelic exclusion. In the current study, we have analyzed single B cells from these and from nonautoimmune mice. In addition, we have cloned and expressed the Ig variable regions of several L chain–included B cells in cell culture. We find that although the number of L chain-included B cells increases as a result of receptor editing, the majority of such cells do not retain an autoreactive HxL chain combination and, therefore, allelic inclusion in itself does not serve as a B cell tolerance mechanism in these autoimmune mice.
机译:除了克隆缺失,克隆无反应性和受体编辑外,还提出了将L链等位基因包涵体作为B细胞耐受机制。据说可以通过表达第二条无害的L链来稀释自身反应性BCR,从而使自身反应性B细胞免于被清除。在自身免疫动物(如易患狼疮的小鼠)中,可激活包含等位基因的B细胞并产生致病性自身抗体。先前我们已经表明,来自患病的新西兰黑/新西兰白F1小鼠的抗DNA杂交瘤表现出近乎完美的等位基因排斥。在当前的研究中,我们已经分析了这些小鼠和非自身免疫小鼠的B细胞。此外,我们已经在细胞培养中克隆并表达了一些包含L链的B细胞的Ig可变区。我们发现,尽管由于受体编辑而使包含L链的B细胞数量增加,但大多数此类细胞并未保留自身反应性HxL链组合,因此,等位基因本身不具有B细胞耐受性这些自身免疫小鼠的体内机制。

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