Gavalchin J, Seder R A, Datta S K
J Immunol. 1987 Jan 1;138(1):128-37.
The incidence of lupus nephritis is low in autoimmune NZB mice, but when they are crossed with normal SWR mice, almost 100% of the female F1 hybrids (SNF1) develop lethal glomerulonephritis. In a previous study we showed that anti-DNA auto-antibodies produced by the SNF1 mice were qualitatively different from those made by the NZB parents with respect to their isotype, charge, and antigenic specificity patterns. Here we studied idiotypic cross-reactions among the 65 monoclonal anti-DNA antibodies that were derived from four NZB and seven SNF1 mice. A library of 15 anti-idiotypic antibodies were prepared by immunizing rabbits with 15 monoclonal anti-DNA antibodies selected from the panel of 65. We identified 10 cross-reactive idiotype (CRI) families among this large collection of autoantibodies. Five of these CRI families were restricted to cationic anti-DNA antibodies that were exclusively of SNF1 origin, and the strongly cross-reacting members were predominantly IgG2b auto-antibodies with the allotype of the normal SWR parent. The cationic anti-DNA CRI families could be grouped into an interrelated cluster called the Id564 cluster. The other five anti-DNA CRI families were not restricted to any particular parental allotype or charge, although two of these CRI were shared exclusively by SNF1-derived autoantibodies and four of these CRI families could also be grouped into an idiotypically interrelated cluster called the Id512 cluster. In the case of seven out of the 10 CRI families, the idiotypic determinants detected were close to the antigen-binding site of the anti-DNA antibodies. The results indicate that the idiotypic repertoire of anti-DNA autoantibodies produced by the SNF1 mice is different from the NZB parents, and potentially pathogenic (cationic) antibodies produced by the SNF1 mice that are encoded by genes from the normal SWR parent can be identified as distinct CRI families. In the accompanying paper we demonstrate the role of these anti-DNA CRI families in the development of lupus nephritis.
自身免疫性新西兰黑(NZB)小鼠中狼疮性肾炎的发病率较低,但当它们与正常的斯威尔(SWR)小鼠杂交时,几乎100%的雌性F1代杂种(SNF1)会发生致命的肾小球肾炎。在之前的一项研究中我们表明,SNF1小鼠产生的抗DNA自身抗体在同种型、电荷和抗原特异性模式方面与NZB亲本产生的抗体在质量上有所不同。在此,我们研究了来自4只NZB和7只SNF1小鼠的65种单克隆抗DNA抗体之间的独特型交叉反应。通过用从65种抗体中挑选出的15种单克隆抗DNA抗体免疫兔子,制备了一个包含15种抗独特型抗体的文库。我们在这一大组自身抗体中鉴定出了10个交叉反应独特型(CRI)家族。其中5个CRI家族仅限于仅源自SNF1的阳离子抗DNA抗体,并且强烈交叉反应的成员主要是具有正常SWR亲本同种异型的IgG2b自身抗体。阳离子抗DNA CRI家族可被归为一个称为Id564簇的相互关联的簇。其他5个抗DNA CRI家族不限于任何特定的亲本同种异型或电荷,尽管其中2个CRI仅由源自SNF1的自身抗体共享,并且这些CRI家族中的4个也可被归为一个称为Id512簇的独特型相互关联的簇。在10个CRI家族中的7个家族中,检测到的独特型决定簇靠近抗DNA抗体的抗原结合位点。结果表明,SNF1小鼠产生的抗DNA自身抗体的独特型库与NZB亲本不同,并且由正常SWR亲本的基因编码的SNF1小鼠产生的潜在致病性(阳离子)抗体可被鉴定为不同的CRI家族。在随附的论文中,我们证明了这些抗DNA CRI家族在狼疮性肾炎发展中的作用。