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利用噬菌体展示组合文库对拮抗型抗人4-1BB单克隆抗体进行人源化

Humanization of antagonistic anti-human 4-1BB monoclonal antibody using a phage-displayed combinatorial library.

作者信息

Lee Unn Hwa, Son Ji Hee, Lee Jeong Jin, Kwon Byungsuk, Park Jeong Woo, Se Kwon Byoung

机构信息

Department of Biological Sciences and Immunomodulation Research Center, University of Ulsan, Ulsan, Korea.

出版信息

J Immunother. 2004 May-Jun;27(3):201-10. doi: 10.1097/00002371-200405000-00004.

Abstract

Anti-4-1BB (CD137) monoclonal antibody (mAb) has been reported to suppress immune responses and to have the potential for use as a therapeutic agent to block autoimmune diseases. Previously, the authors prepared an antagonistic anti-human 4-1BB (CD137) mAb, BBK2. Here the authors report the humanization of BBK2 using a phage display library. Four humanized single-chain Fv (scFv) fragments were selected from a combinatorial library expressing a phage-displayed humanized scFv. They were found to retain the epitope specificity of the original mAb and to have affinities higher than those of the original. Both the soluble and bound forms of the humanized scFv suppressed the proliferation of human peripheral blood mononuclear cells, similar to the original mAb. These results suggest that humanized anti-human 4-1BB scFvs can be used as a valuable reagent for clinical application.

摘要

据报道,抗4-1BB(CD137)单克隆抗体(mAb)可抑制免疫反应,并具有用作治疗剂来阻断自身免疫性疾病的潜力。此前,作者制备了一种拮抗性抗人4-1BB(CD137)单克隆抗体BBK2。在此,作者报道了使用噬菌体展示文库对BBK2进行人源化。从表达噬菌体展示人源化单链Fv(scFv)的组合文库中筛选出四个单链Fv片段。发现它们保留了原始单克隆抗体的表位特异性,并且亲和力高于原始单克隆抗体。人源化单链Fv的可溶性形式和结合形式均能抑制人外周血单个核细胞的增殖,这与原始单克隆抗体相似。这些结果表明,人源化抗人4-1BB单链Fv可作为一种有价值的试剂用于临床应用。

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