Murine pre–B-cell ALL induces T-cell dysfunction not fully reversed by introduction of a chimeric antigen receptor

Author:

Qin Haiying1,Ishii Kazusa1,Nguyen Sang1,Su Paul P.12,Burk Chad R.12,Kim Bong-Hyun34,Duncan Brynn B.1,Tarun Samikasha1,Shah Nirali N.1,Kohler M. Eric1,Fry Terry J.1ORCID

Affiliation:

1. Hematologic Malignancies Section, Pediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD;

2. Howard Hughes Medical Institute, Chevy Chase, MD;

3. Center for Cancer Research Collaborative Bioinformatics Resource, Frederick National Laboratory for Cancer Research, Frederick, MD; and

4. Leidos Biomedical Research, Inc., Frederick, MD

Abstract

Key Points Pre–B-cell ALL induces T-cell dysfunction in vivo, mediated in part by a non–T-cell receptor–linked mechanism. Prior exposure of T cells to pre–B-cell ALL in vivo impairs subsequent functionality of CAR-expressing T cells.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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