Induction of auto-antibody formation in C3H/HeJ mice by cobra venom factor.

P Bloembergen, C Hol, F M Hofhuis, H van Dijk
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引用次数: 1

Abstract

Recently, we demonstrated that lipopolysaccharide (LPS)-hyporesponsive C3H/HeJ mice show a very high background number of splenic antibody-forming cells with specificity for bromelain-treated isologous erythrocytes. This background level was not or only slightly enhanced by LPS injection. In this paper it is reported that the existing response of C3H/HeJ mice is about doubled by treatment of the animals with cobra venom factor (CVF). This increase is very similar to the LPS-induced potentiation of the auto-antibody response of C3H/Tif and other LPS-responder mice. The absence of auto-antibodies in the sera of CVF-treated C3H/HeJ mice, however, points at a different mechanism of B cell activation. The mediation of the CVF-induced stimulation of the B cells of C3H/HeJ mice by covalent C3-glycoprotein complexes and the need for an additional stimulus is discussed.

眼镜蛇毒因子诱导C3H/HeJ小鼠自身抗体的形成。
最近,我们证明了脂多糖(LPS)低反应的C3H/HeJ小鼠显示出非常高的脾脏抗体形成细胞的背景数量,这些细胞对菠萝蛋白酶处理的异体红细胞具有特异性。LPS注射后,该背景水平没有或仅略有提高。本文报道了C3H/HeJ小鼠在用眼镜蛇毒因子(cobra venom factor, CVF)治疗后的现有应答率提高了一倍左右。这种增加与脂多糖诱导C3H/Tif和其他脂多糖应答小鼠自身抗体反应的增强非常相似。然而,cvf处理的C3H/HeJ小鼠血清中缺乏自身抗体,表明B细胞活化的机制不同。讨论了共价c3 -糖蛋白复合物介导cvf诱导的C3H/HeJ小鼠B细胞的刺激,以及是否需要额外的刺激。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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