【摘 要】
:
Systemic lupus erythematosus(SLE)is a chronic,heterogeneous autoimmune disease short of effective therapeutic agents.A multitude of studies of SLE in the last decade have accentuated a central role of
【机 构】
:
Beijing Institute of Biotechnology;Beijing,China
【出 处】
:
第八届国际分子模拟与信息技术应用学术会议
论文部分内容阅读
Systemic lupus erythematosus(SLE)is a chronic,heterogeneous autoimmune disease short of effective therapeutic agents.A multitude of studies of SLE in the last decade have accentuated a central role of the interferon alpha(IFN-α)pathway in SLE pathogenesis.We report here a candidate therapeutic neutralizing antibody,AIA22,with a different binding epitope and discrepant neutralizing profile from the anti-multiple IFN-α subtype antibodies currently in clinical trials.AIA22 specifically interacts with multiple IFN-α subtypes,binds to the type Ⅰ IFN receptor 2(IFNAR2)recognition region of IFN-α(considered a novel antigen epitope),and effectively neutralizes the activity of almost all of the IFN-α subtypes(with the exception of IFN-α7)both in vitro and in vivo.Concurrently,structural modeling and computational design yielded a mutational antibody of AIA22,AlAmut,which exhibited substantially improved neutralizing activity to multiple IFN-α subtypes.
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