Generation of Single-Domain Antibody-Based Recombinant Immunotoxins

Methods Mol Biol. 2022:2446:489-512. doi: 10.1007/978-1-0716-2075-5_25.

Abstract

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.

Keywords: Nanobody; Pseudomonas exotoxin A; Recombinant immunotoxin; Single-domain antibody; Tandem-binding domain.

Publication types

  • Research Support, N.I.H., Intramural

MeSH terms

  • ADP Ribose Transferases / genetics
  • ADP Ribose Transferases / metabolism
  • Bacterial Toxins* / metabolism
  • Exotoxins / metabolism
  • Humans
  • Immunotoxins* / therapeutic use
  • Neoplasms* / drug therapy
  • Recombinant Fusion Proteins / genetics
  • Single-Domain Antibodies*
  • Virulence Factors / metabolism

Substances

  • Bacterial Toxins
  • Exotoxins
  • Immunotoxins
  • Recombinant Fusion Proteins
  • Single-Domain Antibodies
  • Virulence Factors
  • ADP Ribose Transferases