Use of Exogenous Enzymes in Human Therapy: Approved Drugs and Potential Applications.

Recombinant proteins anticancer biologics biopharmaceuticals. cancer enzymatic starvation fibrinolytic therapy pharmaceutical enzymes

Journal

Current medicinal chemistry
ISSN: 1875-533X
Titre abrégé: Curr Med Chem
Pays: United Arab Emirates
ID NLM: 9440157

Informations de publication

Date de publication:
2022
Historique:
received: 23 12 2020
revised: 05 03 2021
accepted: 17 03 2021
pubmed: 15 7 2021
medline: 20 1 2022
entrez: 14 7 2021
Statut: ppublish

Résumé

The development of safe and efficacious enzyme-based human therapies has increased greatly in the last decades, thanks to remarkable advances in the understanding of the molecular mechanisms responsible for different diseases, and the characterization of the catalytic activity of relevant exogenous enzymes that may play a remedial effect in the treatment of such pathologies. Several enzyme-based biotherapeutics have been approved by FDA (the U.S. Food and Drug Administration) and EMA (the European Medicines Agency) and many are undergoing clinical trials. Apart from enzyme replacement therapy in human genetic diseases, which is not discussed in this review, approved enzymes for human therapy find applications in several fields, from cancer therapy to thrombolysis and the treatment, e.g., of clotting disorders, cystic fibrosis, lactose intolerance and collagen-based disorders. The majority of therapeutic enzymes are of microbial origin, the most convenient source due to fast, simple and cost-effective production and manipulation. The use of microbial recombinant enzymes has broadened prospects for human therapy but some hurdles such as high immunogenicity, protein instability, short half-life and low substrate affinity, still need to be tackled. Alternative sources of enzymes, with reduced side effects and improved activity, as well as genetic modification of the enzymes and novel delivery systems are constantly searched. Chemical modification strategies, targeted-and/or nanocarrier-mediated delivery, directed evolution and site-specific mutagenesis, fusion proteins generated by genetic manipulation are the most explored tools to reduce toxicity and improve bioavailability and cellular targeting. This review provides a description of exogenous enzymes that are presently employed for the therapeutic management of human diseases with their current FDA/EMA-approved status, along with those already experimented at the clinical level and potential promising candidates.

Identifiants

pubmed: 34259137
pii: CMC-EPUB-116663
doi: 10.2174/0929867328666210713094722
doi:

Substances chimiques

Pharmaceutical Preparations 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

411-452

Subventions

Organisme : bilateral project of the National Research Council of Italy (CNR)
ID : MD P01.008
Organisme : Russian Foundation for Basic Research (RFBR)
ID : 15-54-78021

Informations de copyright

Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.

Auteurs

Patrizia Cioni (P)

Institute of Biophysics, National Research Council, Via Moruzzi 1, 56124 Pisa,Italy.

Edi Gabellieri (E)

Institute of Biophysics, National Research Council, Via Moruzzi 1, 56124 Pisa,Italy.

Barbara Campanini (B)

Department of Food and Drug, University of Parma, Parco Area delle Scienze 23/A, 43124 Parma,Italy.

Stefano Bettati (S)

Institute of Biophysics, National Research Council, Via Moruzzi 1, 56124 Pisa,Italy.

Samanta Raboni (S)

Institute of Biophysics, National Research Council, Via Moruzzi 1, 56124 Pisa,Italy.

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Classifications MeSH