Generation of Single-Domain Antibody-Based Recombinant Immunotoxins.
Bryan D FlemingMitchell HoPublished in: Methods in molecular biology (Clifton, N.J.) (2022)
The discovery of single-domain antibodies has opened new avenues for drug development. Single-domain antibodies, also known as nanobodies, can access buried epitopes that are inaccessible to conventional antibodies. These antigen-binding domains have a high level of solubility and stability, which makes them well suited for therapeutic development. This chapter will discuss the design, production, and testing of single-domain antibody-based recombinant immunotoxins. Recombinant immunotoxins are chimeric proteins that combine the specificity of an antibody with the ribosomal-inhibitory domain of a bacterial toxin. Immunotoxins using the Pseudomonas exotoxin domain have been well studied in clinical trials. Recently, an anti-CD22 immunotoxin was granted marketing approval for use in patients with relapsed or refractory hairy cell leukemia. This supports the idea that treatment with recombinant immunotoxins can be explored for cancers that have not responded to standard therapies.
Keyphrases
- clinical trial
- acute myeloid leukemia
- cell therapy
- escherichia coli
- single cell
- small molecule
- stem cells
- staphylococcus aureus
- multiple myeloma
- mesenchymal stem cells
- pseudomonas aeruginosa
- hodgkin lymphoma
- transcription factor
- combination therapy
- biofilm formation
- replacement therapy
- phase ii
- structural basis
- smoking cessation