Uwatoko S, Mannik M
Department of Medicine, University of Washington, Seattle 98195.
J Clin Invest. 1988 Sep;82(3):816-24. doi: 10.1172/JCI113684.
The majority of C1q-binding IgG in sera of some patients with systemic lupus erythematosus (SLE) cosediments with monomeric IgG. This study was undertaken to provide definitive proof that the low-molecular weight C1q-binding IgG consists of autoantibodies to C1q. Monomeric C1q-binding IgG was isolated from five SLE plasmas by C1q affinity chromatography and gel filtration. All C1q-binding IgG preparations and their F(ab')2 fragments bound to both C1q and the collagen-like region of C1q by an ELISA. To rule out the possibility that small DNA-antiDNA immune complexes caused this binding activity, Fab' fragments of the C1q-binding IgG preparations were digested with DNase I to degrade any DNA. The Fab' fragments continued to bind to C1q and its collagen-like region after this treatment. C1q-binding IgG was heterogenous on isoelectric focusing. Interaction of C1q-binding IgG with solid-phase C1q was retained in 1 M NaCl, whereas the binding of DNA or heat-aggregated IgG to solid-phase C1q was abrogated or markedly diminished. The association constant of C1q-binding IgG with solid-phase C1q was 2.7 X 10(7) M-1. We conclude that low-molecular weight C1q-binding IgG in the studied patients with SLE consists of autoantibodies to the collagen-like region of C1q.
一些系统性红斑狼疮(SLE)患者血清中的大多数C1q结合性IgG与单体IgG共沉淀。本研究旨在提供确凿证据,证明低分子量C1q结合性IgG由针对C1q的自身抗体组成。通过C1q亲和层析和凝胶过滤从五份SLE血浆中分离出单体C1q结合性IgG。所有C1q结合性IgG制剂及其F(ab')2片段通过酶联免疫吸附测定法(ELISA)与C1q及其C1q胶原样区域结合。为排除小DNA-抗DNA免疫复合物导致这种结合活性的可能性,用脱氧核糖核酸酶I消化C1q结合性IgG制剂的Fab'片段以降解任何DNA。处理后,Fab'片段继续与C1q及其胶原样区域结合。C1q结合性IgG在等电聚焦上具有异质性。C1q结合性IgG与固相C1q的相互作用在1 M氯化钠中得以保留,而DNA或热聚集IgG与固相C1q的结合被消除或显著减弱。C1q结合性IgG与固相C1q的缔合常数为2.7×10(7) M-1。我们得出结论,在所研究的SLE患者中,低分子量C1q结合性IgG由针对C1q胶原样区域的自身抗体组成。