Targeting by affinity-matured recombinant antibody fragments of an angiogenesis associated fibronectin isoform

被引:239
作者
Neri, D
Carnemolla, B
Nissim, A
Leprini, A
Querzè, G
Balza, E
Pini, A
Tarli, L
Halin, C
Neri, P
Zardi, L
Winter, G
机构
[1] Univ Cambridge, Ctr Mrc, Cambridge Ctr Prot Engn, Cambridge CB2 2QH, England
[2] ETH Honggerberg, Inst Mol Biol & Biophys, CH-8093 Zurich, Switzerland
[3] Ist Nazl Ric Canc, Lab Biol Cellulare, I-16132 Genoa, Italy
[4] Univ Siena, Dipartimento Biol Mol, Ctr Didatt Loc Scotte, I-53100 Siena, Italy
关键词
antibody engineering; single-chain antibody; oncofetal protein;
D O I
10.1038/nbt1197-1271
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The oncofetal fibronectin (B-FN) isoform is present in vessels of neoplastic tissues during angiogenesis but not in mature vessels, B-FN could therefore provide a target for diagnostic imaging and therapy of cancer, Phage display libraries have been used to isolate human antibody fragments with pan-species recognition of this isoform, We describe the use of these fragments in nude mice to target an aggressive tumor (grafted Fg murine teratocarcinoma). Imaging in real time was done by infrared photodetection of a chemically coupled fluorophore, The targeting was improved by use of affinity-matured fragments with law kinetic dissociation rates (k(off)=1.5x10(-4) s(-1)) and also by engineering dimeric fragments via a C-terminal amphipathic helix.
引用
收藏
页码:1271 / 1275
页数:5
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