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Manufacturing Chimeric Antigen Receptor CAR T Cells for Adoptive Immunotherapy
Published on: December 17, 2019
CAR Cells beyond Classical CAR T Cells: Functional Properties and Prospects of Application
Elizaveta P Minina1, Dmitry V Dianov1, Saveliy A Sheetikov1
1National Medical Research Centre for Hematology, Ministry of Health of the Russian Federation, Moscow, 125167, Russia.
Abstract:
Chimeric antigen receptors (CARs) are genetically engineered receptors that recognize antigens and activate signaling cascades in a cell. Signal recognition and transmission are mediated by the CAR domains derived from different proteins. T cells carrying CARs against tumor-associated antigens have been used in the development of the CAR T cell therapy, a new approach to fighting malignant neoplasms. Despite its high efficacy in the treatment of oncohematological diseases, CAR T cell therapy has a number of disadvantages that could be avoided by using other types of leukocytes as effector cells. CARs can be expressed in a wide range of cells of adaptive and innate immunity with the emergence or improvement of cytotoxic properties. This review discusses the features of CAR function in different types of immune cells, with a particular focus on the results of preclinical and clinical efficacy studies and the safety of potential CAR cell products.
Insights
Chimeric antigen receptors (CARs) offer a novel approach to cancer therapy by engineering immune cells. This review explores CARs in various immune cells beyond T cells, examining efficacy and safety for potential new treatments.
Area of Science:
- Immunology
- Cellular Engineering
- Oncology
Background:
- Chimeric antigen receptors (CARs) are engineered receptors that direct immune cells to target specific antigens.
- CAR T cell therapy, utilizing T cells engineered with CARs, shows promise in treating hematological malignancies.
- Current CAR T cell therapy faces limitations, prompting exploration of alternative immune effector cells.
Purpose of the Study:
- To review the functional characteristics of CARs in diverse immune cell types.
- To evaluate the preclinical and clinical efficacy of CAR-engineered cells beyond T cells.
- To assess the safety profile of novel CAR-based immunotherapies.
Main Methods:
- Literature review of preclinical studies and clinical trials involving CARs in various immune cells.
- Analysis of CAR domain structures and their impact on signaling and effector functions.
- Comparative assessment of CAR cell therapy efficacy and safety across different leukocyte types.
Main Results:
- CARs can be successfully expressed in various innate and adaptive immune cells, enhancing their cytotoxic potential.
- Studies demonstrate promising efficacy of non-T cell CARs against tumors in preclinical models.
- Initial clinical data suggest potential benefits and manageable safety profiles for alternative CAR cell therapies.
Conclusions:
- Engineering diverse immune cells with CARs offers a promising strategy to overcome limitations of CAR T cell therapy.
- Further research into CAR function across different immune cell types is crucial for developing next-generation cancer immunotherapies.
- CAR cell therapy holds potential for broader applications in treating various cancers, with ongoing investigations into safety and efficacy.
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