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Published on: December 17, 2019
Chimeric Antigen Receptor T-Cell Therapy in Aggressive B-Cell Lymphoma
Mark P Hamilton1, David B Miklos2
1Center for Cancer Cell Therapy, Stanford Cancer Institute, Stanford University School of Medicine, Stanford, CA 94305, USA; Division of Blood and Marrow Transplantation and Cellular Therapy, Department of Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA; Division of Hematology, Department of Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA.
Chimeric antigen receptor (CAR) T-cell therapy offers a revolutionary treatment for aggressive B-cell lymphomas. This review details its clinical use, toxicity, efficacy, resistance mechanisms, and future potential in lymphoma treatment.
Area of Science:
- Oncology
- Immunotherapy
Background:
- Chimeric antigen receptor (CAR) T-cell therapy is a rapidly advancing treatment modality.
- It is increasingly utilized for hematologic malignancies, particularly non-Hodgkin B-cell lymphoma.
Purpose of the Study:
- To provide a comprehensive review of CAR T-cell therapy in aggressive B-cell lymphoma.
- To cover clinical indications, toxicity profiles, efficacy mechanisms, and resistance patterns.
Main Methods:
- Literature review of clinical studies and research on CAR T-cell therapy.
- Analysis of data regarding treatment outcomes, adverse events, and biological mechanisms.
Main Results:
- CAR T-cell therapy demonstrates significant efficacy in treating aggressive B-cell lymphomas.
- Short- and long-term toxicities are well-documented and manageable.
- Mechanisms of both efficacy and tumor resistance are being elucidated.
Conclusions:
- CAR T-cell therapy represents a key therapeutic option for aggressive B-cell lymphoma.
- Ongoing research aims to optimize efficacy, mitigate toxicity, and overcome resistance.
- Future directions include refining CAR T-cell constructs and treatment strategies.
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