Department of Dermatology, Hokkaido University Graduate School of Medicine, N15 W7, Sapporo, 060-8638 Japan.
Am J Pathol. 2010 Feb;176(2):914-25. doi: 10.2353/ajpath.2010.090744. Epub 2009 Dec 30.
Activation of the complement cascade via the classical pathway is required for the development of tissue injury in many autoantibody-mediated diseases. It therefore makes sense to block the pathological action of autoantibodies by preventing complement activation through inhibition of autoantibody binding to the corresponding pathogenic autoantigen using targeted Fab antibody fragments. To achieve this, we use bullous pemphigoid (BP) as an example of a typical autoimmune disease. Recombinant Fabs against the non-collagenous 16th-A domain of type XVII collagen, the main pathogenic epitope for autoantibodies in BP, were generated from antibody repertoires of BP patients by phage display. Two Fabs, Fab-B4 and Fab-19, showed marked ability to inhibit the binding of BP autoantibodies and subsequent complement activation in vitro. In the in vivo experiments using type XVII collagen humanized BP model mice, these Fabs protected mice against BP autoantibody-induced blistering disease. Thus, the blocking of pathogenic epitopes using engineered Fabs appears to demonstrate efficacy and may lead to disease-specific treatments for antibody-mediated autoimmune diseases.
补体级联的经典途径激活是许多自身抗体介导的疾病中组织损伤发展所必需的。因此,通过使用针对 Fab 抗体片段靶向阻断自身抗体与相应致病自身抗原的结合来防止补体激活,从而阻断自身抗体的病理作用是有意义的。为了实现这一目标,我们以天疱疮(BP)为例,这是一种典型的自身免疫性疾病。通过噬菌体展示,从 BP 患者的抗体库中生成了针对 XVII 型胶原非胶原 16 域的重组 Fab,这是 BP 中自身抗体的主要致病表位。两种 Fab,Fab-B4 和 Fab-19,在体外显示出显著抑制 BP 自身抗体结合和随后补体激活的能力。在使用 XVII 型胶原人源化 BP 模型小鼠的体内实验中,这些 Fab 可保护小鼠免受 BP 自身抗体诱导的水疱病。因此,使用工程化 Fab 阻断致病表位似乎显示出疗效,并可能为抗体介导的自身免疫性疾病带来特异性治疗。