The regulatory landscape of CAR T cell dysfunction

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Abstract/Contents

Abstract
Chimeric Antigen Receptor (CAR) T cells have emerged as a promising immunotherapy strategy to target cancer in a subset of patients. T cell exhaustion presents a significant barrier to the progress of CAR T cell therapy development and efficacy. We use a human CAR T cell model system, utilizing the non-exhausting CD19-targeting CD19-28z CAR T cells and the in vitro exhausting GD2-targeting HA-28z CAR T cells, to investigate the genetic interactions and regulation underlying CAR T cell exhaustion and dysfunction. We nominate regulatory transcription factors and enhancer loci that control the expression of exhaustion-associated and -promoting genes and perturb these regulatory networks to modulate the exhaustion phenotype and prevent T cells from exhibiting the hallmarks of exhaustion.

Description

Type of resource text
Form electronic resource; remote; computer; online resource
Extent 1 online resource.
Place California
Place [Stanford, California]
Publisher [Stanford University]
Copyright date 2021; ©2021
Publication date 2021; 2021
Issuance monographic
Language English

Creators/Contributors

Author Gennert, David George
Degree supervisor Chang, Howard Y. (Howard Yuan-Hao), 1972-
Thesis advisor Chang, Howard Y. (Howard Yuan-Hao), 1972-
Thesis advisor Bassik, Michael
Thesis advisor Greenleaf, William James
Thesis advisor Mackall, Crystal
Degree committee member Bassik, Michael
Degree committee member Greenleaf, William James
Degree committee member Mackall, Crystal
Associated with Stanford University, Department of Genetics

Subjects

Genre Theses
Genre Text

Bibliographic information

Statement of responsibility David George Gennert.
Note Submitted to the Department of Genetics.
Thesis Thesis Ph.D. Stanford University 2021.
Location https://purl.stanford.edu/tv531yz5755

Access conditions

Copyright
© 2021 by David George Gennert
License
This work is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported license (CC BY-NC).

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