Wloch M K, Alexander A L, Pippen A M, Pisetsky D S, Gilkeson G S
Department of Medicine, Duke University Medical Center, Durham, USA.
Eur J Immunol. 1996 Sep;26(9):2225-33. doi: 10.1002/eji.1830260939.
To investigate the molecular properties of anti-DNA from lpr mice that express high levels of anti-DNA without immune-mediated nephritis, the sequences of VH and V kappa genes encoding 11 monoclonal anti-DNA antibodies derived from C3H-lpr/lpr (C3H-lpr) mice were studied. All of the C3H-lpr monoclonal anti-DNA bound single-stranded DNA while five also bound double-stranded DNA. Two of the hybridomas were clonally related as determined by Southern analysis and sequencing. Sequence analysis of C3H-lpr anti-DNA revealed the use of VH genes that encode anti-DNA from the MRL-lpr/lpr and (NZB X NZW) F1 mouse models of lupus, although differences occurred in the VH CDR3 amino acid content. In contrast, the V kappa genes from C3H-lpr mice lacked significant identity with previously reported V kappa genes for anti-DNA from lupus models. These results indicate that anti-DNA from C3H-lpr mice differ from anti-DNA from lupus mice with nephritis in patterns of V gene expression and suggest a molecular basis for the lack of pathogenicity of anti-DNA in these mice.
为了研究来自lpr小鼠的抗DNA分子特性,这些lpr小鼠表达高水平的抗DNA但无免疫介导的肾炎,我们研究了编码源自C3H-lpr/lpr(C3H-lpr)小鼠的11种单克隆抗DNA抗体的VH和Vκ基因序列。所有C3H-lpr单克隆抗DNA均结合单链DNA,而其中五种还结合双链DNA。通过Southern分析和测序确定,其中两个杂交瘤具有克隆相关性。C3H-lpr抗DNA的序列分析显示,其使用的VH基因编码来自狼疮的MRL-lpr/lpr和(NZB×NZW)F1小鼠模型的抗DNA,尽管VH CDR3氨基酸含量存在差异。相比之下,C3H-lpr小鼠的Vκ基因与先前报道的狼疮模型抗DNA的Vκ基因缺乏显著同源性。这些结果表明,C3H-lpr小鼠的抗DNA在V基因表达模式上与患有肾炎的狼疮小鼠的抗DNA不同,并提示了这些小鼠中抗DNA缺乏致病性的分子基础。