Single-cell transcriptomics identifies multiple pathways underlying antitumor function of TCR- and CD8αβ-engineered human CD4 + T cells

Author:

Rath Jan A.1ORCID,Bajwa Gagan2ORCID,Carreres Benoit1ORCID,Hoyer Elisabeth2,Gruber Isabelle1ORCID,Martínez-Paniagua Melisa A.3ORCID,Yu Yi-Ru1ORCID,Nouraee Nazila2ORCID,Sadeghi Fatemeh3,Wu Mengfen4,Wang Tao4,Hebeisen Michael1,Rufer Nathalie1,Varadarajan Navin3ORCID,Ho Ping-Chih1ORCID,Brenner Malcolm K.2567ORCID,Gfeller David1ORCID,Arber Caroline125ORCID

Affiliation:

1. Department of Oncology UNIL-CHUV, Lausanne University Hospital, Ludwig Institute for Cancer Research, University of Lausanne, Lausanne, Switzerland.

2. Center for Cell and Gene Therapy, Baylor College of Medicine, Houston Methodist Hospital and Texas Children’s Hospital, Houston, TX, USA.

3. Department of Chemical and Biomolecular Engineering, University of Houston, TX, USA.

4. Biostatistics Shared Resource, Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX, USA.

5. Department of Medicine, Baylor College of Medicine, Houston, TX, USA.

6. Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.

7. Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.

Abstract

TCR-CD8–engineered CD4 + T cells have potent antitumor activity with sustained expression of diverse transcriptional programs.

Funder

National Institutes of Health

National Cancer Institute

Cancer Prevention and Research Institute of Texas

Leukemia and Lymphoma Society

Swiss National Science Foundation

Swiss Government Excellence Scholarship

Krebsforschung Schweiz

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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