Roadmap to affinity-tuned antibodies for enhanced chimeric antigen receptor T cell function and selectivity.
affinity
antibody engineering
chimeric antigen receptor
selectivity
Journal
Trends in biotechnology
ISSN: 1879-3096
Titre abrégé: Trends Biotechnol
Pays: England
ID NLM: 8310903
Informations de publication
Date de publication:
07 2022
07 2022
Historique:
received:
20
10
2021
revised:
16
12
2021
accepted:
17
12
2021
pubmed:
27
1
2022
medline:
14
6
2022
entrez:
26
1
2022
Statut:
ppublish
Résumé
Chimeric antigen receptor (CAR) T cells have revolutionized cancer treatment. CARs use antibody-derived binding domains to redirect T cells to antigens expressed on the surface of cancer cells. However, the high affinity of most currently used CAR-binding domains results in excessive T-cell activation limiting CAR T-cell persistence and the inability to differentiate between antigen-high tumor cells and antigen-low healthy cells. We review recent data on the use of low-affinity CAR-binding domains and evaluate technologies and approaches to engineer and screen low-affinity antibody variants for CAR T-cell development. We propose an ideal workflow for the generation of optimal low-affinity binders derived from existing antibodies to streamline the development of more functional and selective therapeutics.
Identifiants
pubmed: 35078657
pii: S0167-7799(21)00315-2
doi: 10.1016/j.tibtech.2021.12.009
pii:
doi:
Substances chimiques
Receptors, Chimeric Antigen
0
Types de publication
Journal Article
Review
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
875-890Informations de copyright
Copyright © 2022 Elsevier Ltd. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of interests E.R.V., D.A., and T.L. have submitted a patent application ‘Highly selective CD229 chimeric antigen receptor and uses thereof’ (Application Number: 63285843) describing the development of low-affinity CAR-binding domains targeting CD229.