| Literature DB >> 11360829 |
K A Chester1, J Bhatia, G Boxer, S P Cooke, A A Flynn, A Huhalov, A Mayer, R B Pedley, L Robson, S K Sharma, D I Spencer, R H Begent.
Abstract
Single chain Fv antibodies (sFvs) have been produced from filamentous bacteriophage libraries obtained from immunised mice. MFE-23, the most characterised of these sFvs, is reactive with carcinoembryonic antigen (CEA), a glycoprotein that is highly expressed in colorectal adenocarcinomas. MFE-23 has been expressed in bacteria and purified in our laboratory for two clinical trials; a gamma camera imaging trial using 123I-MFE-23 and a radioimmunoguided surgery trial using 125I-MFE-23, where tumour deposits are detected by a hand-held probe during surgery. Both these trials show MFE-23 is safe and effective in localising tumour deposits in patients with cancer. We are now developing fusion proteins which use MFE-23 to deliver a therapeutic moiety; MFE-23::CPG2 targets the enzyme carboxypeptidase G2 (CPG2) for use in the ADEPT (antibody directed enzyme prodrug therapy) system and MFE::TNF alpha aims to reduce sequestration and increase tumor concentrations of systemically administered TNF alpha.Entities:
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Year: 2000 PMID: 11360829 PMCID: PMC3851051 DOI: 10.1155/2000/672706
Source DB: PubMed Journal: Dis Markers ISSN: 0278-0240 Impact factor: 3.434