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Updated: Jun 26, 2026

Initial Evaluation of Antibody-conjugates Modified with Viral-derived Peptides for Increasing Cellular Accumulation and Improving Tumor Targeting
Published on: March 8, 2018
Clinical evidence of efficient tumor targeting based on single-chain Fv antibody selected from a combinatorial
R H Begent1, M J Verhaar, K A Chester
1Department of Clinical Oncology, Royal Free Hospital, School of Medicine, London, UK.
Abstract:
We present a system for cancer targeting based on single-chain Fv (scFv) antibodies selected from combinatorial libraries, produced in bacteria and purified by using an engineered tag. Combinatorial libraries of scFv genes contain great diversity, and scFv antibodies with characteristics optimized for a particular task can be selected from them using filamentous bacteriophage. We illustrate the benefits of this system by imaging patients with carcinoembryonic antigen (CEA)-producing cancers using an iodine-123 labeled scFv anti-CEA selected for high affinity. All known tumor deposits were located, and advantages over current imaging technology are illustrated. ScFvs are produced in a cloned form and can be readily engineered to have localizing and therapeutic functions that will be applicable in cancer and other diseases.
Insights
This study introduces a novel cancer targeting system using engineered single-chain Fv (scFv) antibodies. These antibodies effectively image tumors in patients, offering advantages over existing technologies for cancer diagnosis and treatment.
Area of Science:
- Biotechnology
- Immunology
- Oncology
Background:
- Single-chain variable fragment (scFv) antibodies offer versatile platforms for targeted therapies.
- Combinatorial libraries and phage display enable selection of high-affinity antibodies for specific targets.
Purpose of the Study:
- To develop and validate a system for cancer targeting using engineered scFv antibodies.
- To demonstrate the efficacy of scFv-based imaging in patients with carcinoembryonic antigen (CEA)-producing cancers.
Main Methods:
- Selection of high-affinity anti-CEA scFv antibodies from combinatorial libraries using phage display.
- Production and purification of scFv antibodies in bacteria using an engineered tag.
- Iodine-123 labeling of scFv for SPECT imaging in cancer patients.
Main Results:
- The developed scFv-based system successfully located all known tumor deposits in patients with CEA-producing cancers.
- Iodine-123 labeled anti-CEA scFv demonstrated advantages over current cancer imaging technologies.
- Engineered scFv antibodies showed potential for both diagnostic and therapeutic applications.
Conclusions:
- The presented system provides an effective method for cancer targeting and imaging using engineered scFv antibodies.
- scFv antibodies produced in bacteria offer a scalable and adaptable platform for future cancer diagnostics and therapeutics.
- This approach holds promise for broader applications in oncology and other disease areas.
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