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独特型特异性抑制的细胞基础分析。

Analysis of the cellular basis of idiotype-specific suppression.

作者信息

Ward K, Cantor H, Nisonoff A

出版信息

J Immunol. 1978 Jun;120(6):2016-9.

PMID:307028
Abstract

We have investigated the ability of B and T lymphocyte subclasses from donor mice that produce high levels of anti-Ar antibody but have been suppressed for one idiotypic component (CRI) to induce and maintain idiotypespecific suppression. Our studies indicate: 1) Memory B cells from such mice can preempt virgin CRI+ B cells present in the host from contributing to the anti-Ar response. 2) T cells can also adoptively transfer idiotypespecific suppression. 3) B and T cells do not act synergistically in this transfer of idiotype-specific suppression. 4) Extremely small numbers of Ly23 cells transfer suppression of idiotype and most probably represent true Ts cells. 5) Ly1 cells from hyperimmune idiotypically suppressed donors can induce idiotype-specific suppression. This latter result most likely reflects the induction of idiotype-specific suppressor cells in the host.

摘要

我们研究了来自供体小鼠的B和T淋巴细胞亚类的能力,这些供体小鼠产生高水平的抗Ar抗体,但已被抑制一种独特型成分(CRI),以诱导和维持独特型特异性抑制。我们的研究表明:1)来自此类小鼠的记忆B细胞可以抢先占据宿主中存在的未成熟CRI+B细胞,使其不参与抗Ar反应。2)T细胞也可以过继转移独特型特异性抑制。3)B细胞和T细胞在这种独特型特异性抑制的转移中不协同作用。4)极少量的Ly23细胞转移独特型抑制,很可能代表真正的Ts细胞。5)来自超免疫独特型抑制供体的Ly1细胞可以诱导独特型特异性抑制。后一结果很可能反映了宿主中独特型特异性抑制细胞的诱导。

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