Generation and characterization blocking monoclonal antibody

被引:0
|
作者
Zhuang, Weiliang [1 ]
Zhang, Jianjun [2 ]
Pei, Lili [1 ]
Fang, Shuping [1 ]
Liu, Honghao [1 ]
Wang, Ruixue [2 ]
Su, Yunpeng [1 ]
机构
[1] Novomab Biopharmaceut Inc, Nanjing 210042, Jiangsu, Peoples R China
[2] China Pharmaceut Univ, Nanjing 210009, Jiangsu, Peoples R China
关键词
Autoimmune; SLE; Blys; Antibody; B-LYMPHOCYTE STIMULATOR; SYSTEMIC-LUPUS-ERYTHEMATOSUS; NECROSIS-FACTOR FAMILY; AUTOIMMUNE-DISEASE; SJOGRENS-SYNDROME; BAFF; MICE; BLYS; OVEREXPRESSION; IDENTIFICATION;
D O I
10.1016/j.molimm.2016.08.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The cytokine, B lymphocyte stimulator (Blys) is essential for activation and proliferation of B cells and is involved in the pathogenesis of B-cell mediated autoimmune diseases. Based on its essential activity, Blys may be a potential therapeutic target for human autoimmune diseases. In this article, we have described the development of a novel humanized anti-Blys antibody, NMB04, that binds with high affinity and specificity to both soluble and membrane bound Blys. This monoclonal antibody has the potential to block Blys binding to all its three receptors, TACI, BCMA and BR-3. Further in vivo studies revealed that NMB04 possessed more potent inhibitory activity against human Blys as compared to an existing antibody, Belimumab. Therefore, NMB04 may have potential as a therapeutic candidate targeting autoimmune diseases. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:141 / 147
页数:7
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