Camelid single-domain antibody-fragment engineering for (pre)clinical in vivo molecular imaging applications: adjusting the bullet to its target.

TitleCamelid single-domain antibody-fragment engineering for (pre)clinical in vivo molecular imaging applications: adjusting the bullet to its target.
Publication TypeJournal Article
Year of Publication2013
AuthorsDe Vos, J., N. Devoogdt, T. Lahoutte, and S. Muyldermans
JournalExpert Opin Biol Ther
Volume13
Issue8
Pagination1149-60
Date Published2013 Aug
ISSN1744-7682
KeywordsAnimals, Evaluation Studies as Topic, Humans, Immunoglobulin Fragments, Molecular Imaging, Single-Domain Antibodies
Abstract

INTRODUCTION: Molecular imaging is a fast developing field and there is a growing need for specific imaging tracers in the clinic. Camelid single-domain antibody-fragments (sdAbs) recently emerged as a new class of molecular imaging tracers.AREAS COVERED: We review the importance of molecular imaging in the clinic and the use of camelid sdAbs as in vivo molecular imaging tracers. Interest in imaging tracers based on antibody fragments or man-made protein scaffolds expanded over the last years. Camelid sdAbs are small, monomeric binding fragments that are derived from unique heavy-chain-only antibodies. In vivo imaging studies with sdAbs targeting various cell membrane receptors in different disease models have been reported and more sdAb imaging tracers are under development. The first clinical trial with a camelid sdAb as a molecular imaging tracer targeting the breast cancer marker Human Epidermal growth factor Receptor 2 is currently ongoing.EXPERT OPINION: We expect that the development and use of sdAbs as tracers for both preclinical and clinical molecular imaging applications will become widespread.

DOI10.1517/14712598.2013.800478
Alternate JournalExpert Opin Biol Ther
PubMed ID23675652
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