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建立针对 NMO-IgG 与 AQP4 结合的胞外域的单克隆抗体。

Establishment of monoclonal antibodies against the extracellular domain that block binding of NMO-IgG to AQP4.

机构信息

Department of Pharmacology, School of Medicine, Keio University, 35 Shinanomachi, Shinjyuku-ku, Tokyo 160-8582, Japan.

出版信息

J Neuroimmunol. 2013 Jul 15;260(1-2):107-16. doi: 10.1016/j.jneuroim.2013.03.003.

Abstract

Neuromyelitis optica is a demyelinating disease characterized by a disease-specific autoantibody designated as NMO-IgG that specifically recognizes aquaporin-4, and the binding of NMO-IgG to AQP4 causes the progress of the disease. Prevention of the binding of NMO-IgG, therefore, may alleviate the disease. Here we have developed monoclonal antibodies against AQP4 with a baculovirus display system in order to obtain high affinity monoclonal antibodies against the extracellular domains of AQP4. Our monoclonal antibodies can block the binding of NMO-IgG in spite of their heterogeneity. Taken together, we propose that our monoclonal antibodies can be applied in clinical therapy for NMO patients.

摘要

视神经脊髓炎是一种脱髓鞘疾病,其特征在于存在一种称为 NMO-IgG 的疾病特异性自身抗体,该抗体特异性识别水通道蛋白-4,并且 NMO-IgG 与 AQP4 的结合导致疾病的进展。因此,预防 NMO-IgG 的结合可能会缓解疾病。在这里,我们使用杆状病毒展示系统开发了针对 AQP4 的单克隆抗体,以便获得针对 AQP4 细胞外结构域的高亲和力单克隆抗体。尽管我们的单克隆抗体具有异质性,但它们可以阻断 NMO-IgG 的结合。总之,我们提出我们的单克隆抗体可应用于 NMO 患者的临床治疗。

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