Chimeric antigen receptor (CAR) T cell (CAR-T cell) therapy based on gene editing technology represents a significant breakthrough in personalized immunotherapy for human …
R Chiesa, C Georgiadis, F Syed, H Zhan… - … England Journal of …, 2023 - Mass Medical Soc
Background Cytidine deamination that is guided by clustered regularly interspaced short palindromic repeats (CRISPR) can mediate a highly precise conversion of one nucleotide …
CRISPR-enabled screening is a powerful tool for the discovery of genes that control T cell function and has nominated candidate targets for immunotherapies,,,,–. However, new …
Y Tan, L Shan, L Zhao, B Deng, Z Ling, Y Zhang… - Journal of Hematology & …, 2023 - Springer
Background Donor-derived CD7-directed chimeric antigen receptor (CAR) T cells showed feasibility and early efficacy in patients with refractory or relapsed T-cell acute lymphoblastic …
T-cell malignancies are associated with frequent relapse and high morbidity, which is partly due to the lack of effective or targeted treatment options. To broaden the use of CAR-T cells …
X Yang, B Zhang - Functional & Integrative Genomics, 2023 - Springer
Cancer is one of the leading causes of death worldwide and it has the trend of increase incidence. However, in the past decades, as quickly developed new technologies and …
B Wienert, MK Cromer - Frontiers in Genome Editing, 2022 - frontiersin.org
The discovery of CRISPR has allowed site-specific genomic modification to become a reality and this technology is now being applied in a number of human clinical trials. While this …
A Ren, X Tong, N Xu, T Zhang, F Zhou, H Zhu - Vaccines, 2023 - mdpi.com
T-cell acute lymphoblastic leukemia (T-ALL), a form of T-cell malignancy, is a typically aggressive hematological malignancy with high rates of disease relapse and a poor …