Ward F J, Knies J E, Cunningham C, Harris W J, Staines N A
Infection and Immunity Research Group, King's College London, UK.
Immunology. 1997 Nov;92(3):354-61. doi: 10.1046/j.1365-2567.1997.00359.x.
Cross-reactive idiotypes (CRI) have been detected on anti-DNA autoantibodies associated with lesions typical of systemic lupus erythematosus. In order to analyse the antigenic make up of idiotypes on anti-DNA monoclonal antibodies (mAb) V-88 (IgG1 kappa) and F-423 (IgG3 kappa), derived respectively from an adult (NZB x NZW)F1 and a fetal MRL/Mp-lpr/lpr mouse, a set of overlapping hexapeptides representing the VH and VL regions of mAb V-88 and F-423 were synthesized and reacted with a range of sera in pepscan enzyme-linked immunosorbent assays (ELISA) taken from normal and lupus mouse strains. Serum pools were collected both from normal BALB/c and lupus MRL/Mp-lpr/lpr and (NZB x NZW)F1 mice at 10, 20 and 30 weeks of age and analysed for the presence of spontaneously produced anti-V-region peptide IgM and IgG antibodies. IgM antibodies from both the lupus mice reacted with the same V-region epitopes, and although some epitopes mapped to similar locations in the two mAb, the maps for V-88 and F-423 were not identical. In MRL/Mp-lpr/lpr mice, as lupus disease progressed there was a switch from IgM antibodies to IgG anti-peptide antibodies whose specificity for the peptide antigens coincided with but was better defined than that of the IgM antibodies. The identified idiotopes were located in both complementary determining regions (CDR) and framework region (FR) regions, indicating that some contribute to CRI shared by other related antibodies, while others were unique to either mAb V-88 or F-423. In conclusion, we have dissected and identified a mosaic of antibody V-region idiotopes that contribute to the idiotype of an anti-DNA autoantibody and against which autoantibodies are made naturally in lupus disease.
在与系统性红斑狼疮典型病变相关的抗DNA自身抗体上已检测到交叉反应性独特型(CRI)。为了分析分别源自成年(NZB×NZW)F1小鼠和胎儿MRL/Mp-lpr/lpr小鼠的抗DNA单克隆抗体(mAb)V-88(IgG1 κ)和F-423(IgG3 κ)上独特型的抗原组成,合成了一组代表mAb V-88和F-423的VH和VL区域的重叠六肽,并在肽扫描酶联免疫吸附测定(ELISA)中与取自正常和狼疮小鼠品系的一系列血清反应。从10、20和30周龄的正常BALB/c小鼠、狼疮MRL/Mp-lpr/lpr小鼠和(NZB×NZW)F1小鼠中收集血清池,分析自发产生的抗V区肽IgM和IgG抗体的存在情况。两种狼疮小鼠的IgM抗体都与相同的V区表位反应,尽管一些表位在两种单克隆抗体中映射到相似位置,但V-88和F-423的图谱并不相同。在MRL/Mp-lpr/lpr小鼠中,随着狼疮疾病的进展,出现了从IgM抗体到IgG抗肽抗体的转换,其对肽抗原的特异性与IgM抗体一致,但比IgM抗体更明确。鉴定出的独特位位于互补决定区(CDR)和框架区(FR)区域,这表明一些独特位促成了其他相关抗体共享的CRI,而其他独特位则是mAb V-88或F-423所特有的。总之,我们剖析并鉴定了抗体V区独特位的镶嵌图谱,这些独特位促成了抗DNA自身抗体的独特型,并且在狼疮疾病中会自然产生针对这些独特位的自身抗体。