Preparation of phage antibodies to the ED-A domain of human fibronectin

被引:18
作者
Borsi, L
Castellani, P
Allemanni, G
Neri, D
Zardi, L
机构
[1] Ist Nazl Ric Canc, Cell Biol Lab, I-16132 Genoa, Italy
[2] ETH Zurich, Inst Mol Biol & Biophys, CH-8093 Zurich, Switzerland
关键词
D O I
10.1006/excr.1998.3946
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The fibronectin (FN) isoform containing the alternative spliced ED-A domain is much more expressed in fetal, tumoral, and regenerating tissues than in normal adult tissues. The ED-A containing FN is up-regulated by numerous cytokines, such as TGF-beta, and, although in normal adult liver the ED-A domain is undetectable, in regenerating rat liver the expression of ED-A is increased and mediates the conversion of fat storing cells to myofibroblasts. Here we describe the selection from a phage display library and the characterization of human antibody fragments directed against the EDA sequence of FN, As they can be easily radiolabeled with P-32, these antibodies are very highly sensitive reagents for the determination of ED-A levels in tissues and biological fluids; in fact, use of these scFv induced a more than 10-fold increase in sensitivity with respect to the murine monoclonal IST-9. The possibility of preparing a range of human engineered antibodies should facilitate the development of antibody reagents with suitable pharmacokinetics, valency, functional affinity, and effector functions and that could be useful for clinical purposes. (C) 1998 Academic Press.
引用
收藏
页码:244 / 251
页数:8
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