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通过与新制癌菌素偶联的抗独特型抗体对人抗DNA抗体产生进行体外操作。

In vitro manipulation of human anti-DNA antibody production by anti-idiotypic antibodies conjugated with neocarzinostatin.

作者信息

Sasaki T, Tamate E, Muryoi T, Takai O, Yoshinaga K

机构信息

Second Department of Internal Medicine, Tohoku University School of Medicine, Sendai, Japan.

出版信息

J Immunol. 1989 Feb 15;142(4):1159-65.

PMID:2521660
Abstract

Anti-DNA Id, 0-81, consist of 5 to 51% of Id in human anti-ssDNA antibodies; NE-1-Id shares 2 to 20% of those in anti-dsDNA antibodies. Thus, both 0-81-Id and NE-1-Id are of the cross-reactive Id that are commonly present among anti-DNA antibodies. In order to manipulate the production of anti-DNA antibodies by human PBL, we used mouse antiidiotypic mAb or those conjugated with a cytotoxic agent, neocarzinostatin. Treatment with the conjugates caused profound suppression of anti-ssDNA and anti-dsDNA antibody synthesis related to 0-81- and NE-1-Id. This was attributed to the specific killing of the clones bearing anti-DNA Id among the lymphocytes, evidenced by the indirect rosette formation tests. The Id-mediated suppression was not solely due to selective elimination of Id-positive B cells, because 50 to 92% of anti-DNA antibodies were suppressed by treatment with the conjugates. This was supported by flow cytometry analysis that showed a decrease of anti-Id-reactive cells when T cells were treated with the conjugates. This method, then, will permit an analysis of the question as to whether T cells reactive to anti-idiotypic antibodies might participate in the regulatory mechanism for anti-DNA production and, in addition, may lead to a new therapy for SLE.

摘要

抗DNA独特型0-81,占人抗单链DNA抗体中独特型的5%至51%;NE-1-独特型在抗双链DNA抗体中占2%至20%。因此,0-81-独特型和NE-1-独特型均为抗DNA抗体中常见的交叉反应性独特型。为了调控人外周血淋巴细胞产生抗DNA抗体,我们使用了小鼠抗独特型单克隆抗体或与细胞毒性药物新制癌菌素偶联的抗体。用这些偶联物处理可显著抑制与0-81-和NE-1-独特型相关的抗单链DNA和抗双链DNA抗体的合成。这归因于淋巴细胞中携带抗DNA独特型的克隆被特异性杀伤,间接花环形成试验证明了这一点。独特型介导的抑制并非仅仅由于Id阳性B细胞的选择性清除,因为用偶联物处理可抑制50%至92%的抗DNA抗体。流式细胞术分析支持了这一点,该分析显示用偶联物处理T细胞时抗独特型反应性细胞减少。那么,这种方法将有助于分析对抗独特型抗体有反应的T细胞是否可能参与抗DNA产生的调节机制,此外,可能会带来一种治疗系统性红斑狼疮的新疗法。

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