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Updated: May 7, 2026

Validation of Nanobody and Antibody Based In Vivo Tumor Xenograft NIRF-imaging Experiments in Mice Using Ex Vivo Flow Cytometry and Microscopy
Published on: April 6, 2015
Targeting tumors with nanobodies for cancer imaging and therapy
Sabrina Oliveira1, Raimond Heukers, Jirawas Sornkom
1Division of Cell Biology, Department of Biology, Faculty of Science, Utrecht University, Padualaan 8, 3584 CH Utrecht, The Netherlands; Department of Pathology, University Medical Center Utrecht, Heidelberglaan 100, 3584 CX Utrecht, The Netherlands.
Abstract:
The use of monoclonal antibodies has revolutionized both cancer therapy and cancer imaging. Antibodies have been used to directly inhibit tumor cell proliferation or to target drugs to tumors. Also in molecular imaging, monoclonal antibodies have found their way to the clinic. Nevertheless, distribution within tumors is hampered by their size, leading to insufficient efficacy of cancer treatment and irregular imaging. An attractive alternative for monoclonal antibodies are nanobodies or VHHs. These are the variable domain of heavy-chain antibodies from animals from the Camelidae family that were first discovered in 1993. Stimulated by the ease of nanobody selection, production, and low immunogenicity potential, a number of nanobodies specific to different disease-related targets have been developed. For cancer therapy, nanobodies have been employed as antagonistic drugs, and more recently, as targeting moieties of effector-domaINS and of drug delivery systems. In parallel, nanobodies have also been employed for molecular imaging with modalities such as nuclear and optical imaging. In this review, we discuss recent developments in the application of nanobodies as targeting moieties in cancer therapy and cancer imaging. With such a wide range of successful applications, nanobodies have become much more than simple antagonists.
Insights
Nanobodies offer a promising alternative to monoclonal antibodies for cancer therapy and imaging due to their small size and ease of production. These VHHs are effective targeting moieties for drug delivery and molecular imaging, improving treatment efficacy and image resolution.
Area of Science:
- Biotechnology
- Oncology
- Immunology
Background:
- Monoclonal antibodies have advanced cancer therapy and imaging but face limitations due to their large size, impacting tumor penetration and efficacy.
- Nanobodies (VHHs), derived from camelid heavy-chain antibodies, present an attractive alternative with potential for improved tumor targeting.
Purpose of the Study:
- To review recent advancements in the application of nanobodies as targeting moieties in cancer therapy and molecular imaging.
- To highlight the advantages of nanobodies over traditional monoclonal antibodies in oncology.
Main Methods:
- Literature review of studies on nanobody development and application in cancer research.
- Analysis of nanobody use in preclinical and clinical settings for therapy and imaging modalities.
- Discussion of nanobody characteristics, including selection, production, and immunogenicity.
Main Results:
- Nanobodies have been successfully employed as antagonistic drugs, targeting moieties for drug delivery systems, and in molecular imaging (nuclear and optical).
- Their small size facilitates better tumor penetration compared to monoclonal antibodies, potentially leading to improved therapeutic outcomes and imaging quality.
- Nanobodies demonstrate ease of selection, production, and low immunogenicity, making them versatile tools in cancer research.
Conclusions:
- Nanobodies are emerging as powerful tools in oncology, offering significant advantages over monoclonal antibodies for both cancer treatment and diagnostic imaging.
- Their versatility and efficacy position nanobodies as a key technology for future advancements in personalized cancer medicine.
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