Roadmap to affinity-tuned antibodies for enhanced chimeric antigen receptor T cell function and 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
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

875-890

Informations 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.

Auteurs

Erica R Vander Mause (ER)

Department of Microbiology and Immunology, University of Maryland, Baltimore, MD 21201, USA; Department of Pharmaceutics and Pharmaceutical Chemistry, University of Utah, Salt Lake City, UT 84112, USA; A2 Biotherapeutics, Agoura Hills, CA, 91301, USA. Electronic address: evandermause@a2biotherapeutics.com.

Djordje Atanackovic (D)

Transplant and Cellular Therapy Program, Department of Medicine, University of Maryland School of Medicine and Greenebaum Comprehensive Cancer Center, Baltimore, MD 21201, USA.

Carol S Lim (CS)

Department of Pharmaceutics and Pharmaceutical Chemistry, University of Utah, Salt Lake City, UT 84112, USA.

Tim Luetkens (T)

Department of Microbiology and Immunology, University of Maryland, Baltimore, MD 21201, USA; Transplant and Cellular Therapy Program, Department of Medicine, University of Maryland School of Medicine and Greenebaum Comprehensive Cancer Center, Baltimore, MD 21201, USA.

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