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Murine monoclonal antibodies to DNA. A comparison of MRL/lpr NZB/W and chronically graft-versus-host-diseased mice.

机译:鼠抗DNA单克隆抗体。 MRL / lpr NZB / W与慢性移植物抗宿主病小鼠的比较。

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摘要

Hybridomas producing monoclonal antibodies to DNA were prepared from NZB/W F1 (n = 20), MRL/lpr (n = 13), mice with a chronical graft versus-host-disease (GVHD) (n = 8) and polyclonally stimulated mice (n = 9). Screening was performed by means of an anti-DNA ELISA. Reaction patterns in four different anti-DNA assays (anti-DNA ELISA, indirect immunofluorescence on Crithidia luciliae, PEG assay and Farr assay) as well as avidity and cross-reactivity of these monoclonals were studied in relation to anti-DNA (sub)class and murine origin of the clones. It was found that monoclonal anti-DNA derived from mice with chronic GVHD did not differ from monoclonal anti-DNA derived from NZB/W F1 or MRL/lpr mice, with respect to isotype distribution, avidity towards DNA, cross-reactivity and assay behaviour in the anti-DNA assays mentioned before. In contrast, monoclonal anti-DNA obtained from polyclonally stimulated mice were all of the IgM isotype and displayed a stronger cross-reactive behaviour than the other three models. Altogether, these results exclude the possibility that anti-DNA in the GVHD mice originates from the non-specific pool of natural autoantibodies and further emphasize the relevance of chronic GVHD as a murine model of systemic lupus erythematosus.
机译:从NZB / W F1(n = 20),MRL / lpr(n = 13),患有慢性移植物抗宿主病(GVHD)的小鼠(n = 8)和经多克隆刺激的小鼠制备产生针对DNA的单克隆抗体的杂交瘤(n = 9)。借助于抗DNA ELISA进行筛选。研究了四种不同的抗DNA检测的反应模式(抗DNA ELISA,在光闪夜蛾上的间接免疫荧光,PEG检测和Farr检测)以及与抗DNA(亚)类相关的这些单克隆的亲和力和交叉反应性和克隆的鼠源。发现同种型分布,对DNA的亲和力,交叉反应性和测定行为在慢性GVHD小鼠中得到的单克隆抗DNA与NZB / W F1或MRL / lpr小鼠得到的单克隆抗DNA没有区别。在前面提到的抗DNA分析中。相反,从多克隆刺激小鼠获得的单克隆抗DNA均为IgM同型,并且比其他三个模型表现出更强的交叉反应性。总之,这些结果排除了GVHD小鼠中抗DNA来源于天然自身抗体的非特异性库的可能性,并进一步强调了慢性GVHD作为系统性红斑狼疮鼠模型的相关性。

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