Phage display antibody libraries: A robust approach for generation of recombinant human monoclonal antibodies.
Diagnostics
Monoclonal antibodies
Phage display
Therapeutic antibodies
Journal
International journal of biological macromolecules
ISSN: 1879-0003
Titre abrégé: Int J Biol Macromol
Pays: Netherlands
ID NLM: 7909578
Informations de publication
Date de publication:
15 Aug 2019
15 Aug 2019
Historique:
received:
26
04
2019
revised:
02
06
2019
accepted:
02
06
2019
pubmed:
7
6
2019
medline:
18
12
2019
entrez:
7
6
2019
Statut:
ppublish
Résumé
Monoclonal antibodies (mAbs) and their derivatives have achieved remarkable success as medicine, targeting both diagnostic and therapeutic applications associated with communicable and non-communicable diseases. In the last 3 to 4 decades, tremendous success has been manifested in the field of cancer therapy, autoimmune diseases, cardiovascular and infectious diseases. MAbs are the fastest growing class of biopharmaceuticals, with more than 25 derivatives are in clinical use and 7 of these have been isolated through phage display technology. Phage display technology has gained impetus in the field of medical and health sciences, as a large repertoire of diverse recombinant antibodies, targeting various antigens have been generated in a short span of time. A prominent number of phage display derived antibodies are already approved for therapy and significant numbers are currently in clinical trials. In this review we have discussed the various strategies employed for generation of monoclonal antibodies; their advantages, limitations and potential therapeutic applications. We also discuss the potential of phage display antibody libraries in isolation of monoclonal antibodies.
Identifiants
pubmed: 31170490
pii: S0141-8130(19)33085-5
doi: 10.1016/j.ijbiomac.2019.06.006
pii:
doi:
Substances chimiques
Antibodies, Monoclonal
0
Recombinant Proteins
0
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
907-918Informations de copyright
Copyright © 2019 Elsevier B.V. All rights reserved.