High CAR intensity of expression confers enhanced antitumor effect against lymphoma without functional exhaustion
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cancer Research,Molecular Biology,Molecular Medicine
Link
https://www.nature.com/articles/s41417-022-00518-6.pdf
Reference60 articles.
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2. Grover NS, Savoldo B. Challenges of driving CD30-directed CAR-T cells to the clinic. BMC Cancer. 2019;19:1–8.
3. Dai H, Wang Y, Lu X, Han W. Chimeric antigen receptors modified T-cells for cancer therapy. J Natl Cancer Inst. 2016;108. https://doi.org/10.1093/jnci/djv439.
4. Strati P, Neelapu SS. Chimeric antigen receptor–engineered T cell therapy in lymphoma. Curr Oncol Rep. 2019;21. https://doi.org/10.1007/s11912-019-0789-z.
5. Kochenderfer JN, Dudley ME, Kassim SH, Somerville RPT, Carpenter RO, Maryalice SS, et al. Chemotherapy-refractory diffuse large B-cell lymphoma and indolent B-cell malignancies can be effectively treated with autologous T cells expressing an anti-CD19 chimeric antigen receptor. J Clin Oncol. 2015;33:540–9.
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1. Correction to: High CAR intensity of expression confers enhanced antitumor effect against lymphoma without functional exhaustion;Cancer Gene Therapy;2022-12-02
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