抗体
抗原
CD19
分子生物学
重组DNA
单克隆抗体
化学
生物
病毒学
免疫学
基因
生物化学
作者
B Bejcek,Duo Wang,Erica Berven,Christopher A. Pennell,S C Peiper,Sibrandes Poppema,Fatih M. Uckun,John H. Kersey
出处
期刊:PubMed
日期:1995-06-01
卷期号:55 (11): 2346-51
被引量:25
摘要
Antibodies that recognize antigens restricted to leukemia, lymphoma, and normal hematopoietic cells represent a unique opportunity to develop therapeutics, because they have the potential for relatively selective treatment of these diseases. Antibodies that recognize the CD19 antigen found on normal and malignant B cells, but not on stem cells, have been used to develop immunoconjugates. However, these conjugates are large and might be suboptimal in tumor penetration when compared to molecules using smaller single chain Fv (scFv) antibody fragments. scFv has the advantage of being a molecularly engineered homogeneous molecule. In this report, we demonstrate the cloning, expression, and binding of three anti-CD19 antibodies as scFvs. All three scFvs were successfully cloned and expressed. FVS191, derived from cell line B43, and FVS192, derived from SJ25C1, were properly refolded and bound CD19 antigen in FACS competition assays. These anti-CD19 scFv should be useful in the further development of diagnostic and therapeutic molecules.
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