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ConvertibleCARs: A chimeric antigen receptor system for flexible control of activity and antigen targeting.


ABSTRACT: We have developed a chimeric antigen receptor (CAR) platform that functions as a modular system to address limitations of traditional CAR therapies. An inert form of the human NKG2D extracellular domain (iNKG2D) was engineered as the ectodomain of the CAR to generate convertibleCARTM-T cells. These cells were specifically directed to kill antigen-expressing target cells only in the presence of an activating bispecific adapter comprised of an iNKG2D-exclusive ULBP2-based ligand fused to an antigen-targeting antibody (MicAbodyTM). Efficacy against Raji tumors in NSG mice was dependent upon doses of both a rituximab-based MicAbody and convertibleCAR-T cells. We have also demonstrated that the exclusive ligand-receptor partnering enabled the targeted delivery of a mutant form of IL-2 to selectively promote the expansion of convertibleCAR-T cells in vitro and in vivo. By altering the Fv domains of the MicAbody or the payload fused to the orthogonal ligand, convertibleCAR-T cells can be readily targeted or regulated.

SUBMITTER: Landgraf KE 

PROVIDER: S-EPMC7283332 | biostudies-literature | 2020 Jun

REPOSITORIES: biostudies-literature

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convertibleCARs: A chimeric antigen receptor system for flexible control of activity and antigen targeting.

Landgraf Kyle E KE   Williams Steven R SR   Steiger Daniel D   Gebhart Dana D   Lok Stephen S   Martin David W DW   Roybal Kole T KT   Kim Kaman Chan KC  

Communications biology 20200609 1


We have developed a chimeric antigen receptor (CAR) platform that functions as a modular system to address limitations of traditional CAR therapies. An inert form of the human NKG2D extracellular domain (iNKG2D) was engineered as the ectodomain of the CAR to generate convertibleCAR<sup>TM</sup>-T cells. These cells were specifically directed to kill antigen-expressing target cells only in the presence of an activating bispecific adapter comprised of an iNKG2D-exclusive ULBP2-based ligand fused t  ...[more]

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