Chimeric antigen receptors for T-cell based therapy

Eleanor J. Cheadle, Vicky Sheard, Andreas A. Hombach, Markus Chmielelewski, Tobias Riet, Cor Berrevoets, Erik Schooten, Cor Lamers, Hinrich Abken, Reno Debets, David E. Gilham

Research output: Chapter/Conference proceedingChapterAcademic

41 Citations (Scopus)

Abstract

The Chimeric Antigen Receptor (CAR) consists of an antibody-derived targeting domain fused with T-cell signaling domains that, when expressed by a T-cell, endows the T-cell with antigen specificity determined by the targeting domain of the CAR. CARs can potentially redirect the effector functions of a T-cell towards any protein and nonprotein target expressed on the cell surface as long as an antibody or similar targeting domain is available. This strategy thereby avoids the requirement of antigen processing and presentation by the target cell and is applicable to nonclassical T-cell targets like carbohydrates. This circumvention of HLA-restriction means that the CAR T-cell approach can be used as a generic tool broadening the potential of applicability of adoptive T-cell therapy. Proof-of-principle studies focusing upon the investigation of the potency of CAR T-cells have primarily focused upon the genetic modification of human and mouse T-cells for therapy. This chapter focuses upon methods to modify T-cells from both species to generate CAR T-cells for functional testing.
Original languageEnglish
Title of host publicationAntibody engineering
Subtitle of host publicationmethods and protocols
EditorsPatrick Chames
PublisherHumana Press
Chapter36
Pages645-666
Number of pages22
EditionSecond
ISBN (Print)9781617799730
Publication statusPublished - 2012

Publication series

SeriesMethods in Molecular Biology
Volume907
ISSN1064-3745

Research programs

  • EMC MM-03-86-08

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