抗体
免疫球蛋白轻链
单克隆抗体
抗原
多发性骨髓瘤
分子生物学
生物
免疫学
癌症研究
化学
作者
Keita Sato,Masayuki Tsuchiya,José W. Saldanha,Yasuo Koishihara,Yoshiyuki Ohsugi,Tadamitsu Kishimoto,Mary M. Bendig
出处
期刊:PubMed
日期:1993-02-15
卷期号:53 (4): 851-6
被引量:91
摘要
The mouse PM-1 monoclonal antibody binds to the human interleukin 6 receptor, inhibits IL-6 functions, and shows strong antitumor cell activity against multiple myeloma cells. In order to be effective as a therapeutic agent administered to human patients in repeated doses, reshaped human PM-1 antibodies consisting of human REI-based light chain and NEW-based heavy chain variable regions were designed and constructed with the assistance of a structural model of the mouse PM-1 variable regions. The best reshaped human PM-1 antibody is equivalent to mouse or chimeric PM-1 antibody in terms of antigen binding and growth inhibition against multiple myeloma cells. Only a few minor changes in the human framework regions were required to recreate the mouse PM-1 antigen-binding site within a human antibody. The reshaped human PM-1 antibody, therefore, could be efficacious in human multiple myeloma patients.
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