Human anti-human IL-18 antibody recognizing the IL-18-binding site 3 with IL-18 signaling blocking activity

被引:21
作者
Hamasaki, T
Hashiguchi, S
Ito, Y
Kato, Z
Nakanishi, K
Nakashima, T
Sugimura, K
机构
[1] Kagoshima Univ, Fac Engn, Dept Bioengn, Kagoshima 8900065, Japan
[2] Gifu Univ, Grad Sch Med, Dept Pediat, Gifu 5011194, Japan
[3] Hyogo Med Univ, Dept Immunol & Med Zool, Nishinomiya, Hyogo 6638501, Japan
[4] Chemosero Therapeut Res Inst, Kumamoto 8691298, Japan
[5] Japan Sci & Technol Corp, Core Res Evolut Sci & Technol, Tokyo, Japan
关键词
allergy; epitope mapping; interleukin-18; human antibody; phage display;
D O I
10.1093/jb/mvi148
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
IL-18 is an important regulator in both innate and acquired immune responses. The aberrant expression of IL-18 is associated with severe inflammatory conditions, such as autoimmune diseases and allergies. Thus, human antibodies with inhibitory activity on IL-18 signaling may be useful for therapeutic applications. We report here the first establishment of an antagonistic anti-IL-18 complete human antibody, h18-108, employing a human single chain antibody (scFv)-displaying phage library. The h18-108 scFv inhibited the IFN-gamma production of a human myelomonocytic cell line, KG-1. Flow cytometry analysis showed that h18-108 blocked the binding of IL-18 to KG-l cells. Epitope mapping analysis using two kinds of random peptide-displaying phage libraries and an IL-18 alanine mutant (D98A) demonstrated that the h18-108 scFv binds to the site 3 of IL-18, which is suggested to be an association site with the IL-18 receptor P. The complete human Fab and IgG forms of h18-108 have been successfully constructed to attain increases in both binding affinity and inhibitory activity.
引用
收藏
页码:433 / 442
页数:10
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