Human toxin-based recombinant immunotoxins/chimeric proteins as a drug delivery system for targeted treatment of human diseases
- PMID: 21453191
- DOI: 10.1517/17425247.2011.566269
Human toxin-based recombinant immunotoxins/chimeric proteins as a drug delivery system for targeted treatment of human diseases
Abstract
Introduction: The development of specific immunosuppressive reagents remains the major goal in the treatment of human diseases. One such approach is the use of recombinant immunotoxins/chimeric proteins, composed of targeting and killing moieties, fused at the cDNA level. Most of these 'magic bullets' use bacterial or plant toxins to induce cell death. These toxins are extremely potent, but they also cause severe toxicity and systemic side effects that limit the maximal doses given to patients. Moreover, being of non-human origin, they are highly immunogenic, and the resulting neutralizing antibody production impairs their efficacy.
Areas covered: This review describes recombinant immunotoxins/chimeric proteins composed of the classical delivering, cell-targeting molecules, fused to highly cytotoxic human proteins capable of generating an intense apoptotic response within the target cell. This review focuses on the new 'Human Killing Moieties' of these targeted proteins and describes recent progress in the development of these promising molecules.
Expert opinion: Human toxin-based immunotoxins/chimeric proteins for the targeted delivery of drugs are still in their early stages of development. However, they are certain to advance in the very near future to become an extra weapon in the everlasting war against human diseases, mainly cancer.
Similar articles
-
Patents on immunotoxins and chimeric toxins for the treatment of cancer.Recent Pat Drug Deliv Formul. 2007;1(2):105-15. doi: 10.2174/187221107780831932. Recent Pat Drug Deliv Formul. 2007. PMID: 19075878 Review.
-
Recombinant antibody fragments and immunotoxin fusions for cancer therapy.In Vivo. 2000 Jan-Feb;14(1):21-7. In Vivo. 2000. PMID: 10757057 Review.
-
Immunotoxins and cytokine toxin fusion proteins.Semin Immunol. 1990 Nov;2(6):467-79. Semin Immunol. 1990. PMID: 2104283 Review.
-
Antibody targeted drugs as cancer therapeutics.Nat Rev Drug Discov. 2006 Feb;5(2):147-59. doi: 10.1038/nrd1957. Nat Rev Drug Discov. 2006. PMID: 16424916 Review.
-
Targeted therapy of cancer using diphtheria toxin-derived immunotoxins.Drug Discov Today. 2008 Sep;13(17-18):807-15. doi: 10.1016/j.drudis.2008.06.017. Epub 2008 Aug 21. Drug Discov Today. 2008. PMID: 18678276 Review.
Cited by
-
Exploiting the Endogenous Ubiquitin Proteasome System in Targeted Cancer Treatment.Cancers (Basel). 2022 Dec 30;15(1):256. doi: 10.3390/cancers15010256. Cancers (Basel). 2022. PMID: 36612252 Free PMC article.
-
Two Simple Methods for Optimizing the Production of "Difficult-to-Express" GnRH-DFF40 Chimeric Protein.Adv Pharm Bull. 2019 Aug;9(3):423-431. doi: 10.15171/apb.2019.050. Epub 2019 Aug 1. Adv Pharm Bull. 2019. PMID: 31592077 Free PMC article.
-
Targeted Toxins for the Treatment of Prostate Cancer.Biomedicines. 2021 Aug 9;9(8):986. doi: 10.3390/biomedicines9080986. Biomedicines. 2021. PMID: 34440190 Free PMC article. Review.
-
Functional production of a soluble and secreted single-chain antibody by a bacterial secretion system.PLoS One. 2014 May 13;9(5):e97367. doi: 10.1371/journal.pone.0097367. eCollection 2014. PLoS One. 2014. PMID: 24824752 Free PMC article.
-
Combining flagellin and human β-defensin-3 to combat bacterial infections.Front Microbiol. 2014 Dec 9;5:673. doi: 10.3389/fmicb.2014.00673. eCollection 2014. Front Microbiol. 2014. PMID: 25538693 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources