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Article ; Online: Enhancing chimeric antigen receptor T cell therapy by modulating the p53 signaling network with Δ133p53α.

Roselle, Christopher / Horikawa, Izumi / Chen, Linhui / Kelly, Andre R / Gonzales, Donna / Da, Tong / Wellhausen, Nils / Rommel, Philipp C / Baker, Daniel / Suhoski, Megan / Scholler, John / O'Connor, Roddy S / Young, Regina M / Harris, Curtis C / June, Carl H

Proceedings of the National Academy of Sciences of the United States of America

2024  Volume 121, Issue 10, Page(s) e2317735121

Abstract: Chimeric antigen receptor (CAR) T cell dysfunction is a major barrier to achieving lasting remission in hematologic cancers, especially in chronic lymphocytic leukemia (CLL). We have shown previously that Δ133p53α, an endogenous isoform of the human TP53 ...

Abstract Chimeric antigen receptor (CAR) T cell dysfunction is a major barrier to achieving lasting remission in hematologic cancers, especially in chronic lymphocytic leukemia (CLL). We have shown previously that Δ133p53α, an endogenous isoform of the human TP53 gene, decreases in expression with age in human T cells, and that reconstitution of Δ133p53α in poorly functional T cells can rescue proliferation [A. M. Mondal
MeSH term(s) Humans ; Immunotherapy, Adoptive/methods ; Leukemia, Lymphocytic, Chronic, B-Cell/genetics ; Leukemia, Lymphocytic, Chronic, B-Cell/therapy ; Receptors, Chimeric Antigen/genetics ; Receptors, Chimeric Antigen/metabolism ; Tumor Suppressor Protein p53/genetics ; Tumor Suppressor Protein p53/metabolism ; Antigens, CD19 ; Cell- and Tissue-Based Therapy ; Receptors, Antigen, T-Cell/genetics ; Receptors, Antigen, T-Cell/metabolism
Chemical Substances Receptors, Chimeric Antigen ; Tumor Suppressor Protein p53 ; Antigens, CD19 ; Receptors, Antigen, T-Cell
Language English
Publishing date 2024-02-26
Publishing country United States
Document type Journal Article
ZDB-ID 209104-5
ISSN 1091-6490 ; 0027-8424
ISSN (online) 1091-6490
ISSN 0027-8424
DOI 10.1073/pnas.2317735121
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