Abstract
Immunotherapy has been growing in the past decade as a therapeutic alternative for cancer treatment. In this chapter, we deal with CAR-T cells, genetically engineered autologous T cells to express a chimeric receptor specific for an antigen expressed on tumor cell surface. While this type of personalized therapy is revolutionizing cancer treatment, especially B cell malignancies, it has some challenging limitations. Here, we discuss the basic immunological and technological aspects of CAR-T cell therapy, the limitations that have compromised its efficacy and safety, and the current proposed strategies to overcome these limitations, thereby allowing for greater therapeutic application of CAR-T cells.
Keywords:
CAR-T cells; Chimeric antigen receptor; Immunotherapy; T cells.
Publication types
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Research Support, Non-U.S. Gov't
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Review
MeSH terms
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Animals
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Antigens, Neoplasm
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Cellular Microenvironment / genetics
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Cellular Microenvironment / immunology
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Genetic Engineering
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Humans
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Immunomodulation
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Immunotherapy, Adoptive* / adverse effects
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Immunotherapy, Adoptive* / methods
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Immunotherapy, Adoptive* / standards
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Immunotherapy, Adoptive* / trends
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Lymphocyte Activation / genetics
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Lymphocyte Activation / immunology
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Neoplasms / immunology*
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Neoplasms / therapy*
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Receptors, Antigen, T-Cell / genetics
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Receptors, Antigen, T-Cell / metabolism
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Receptors, Chimeric Antigen / genetics
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Receptors, Chimeric Antigen / metabolism
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Research Design
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T-Lymphocytes / immunology*
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T-Lymphocytes / metabolism*
Substances
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Antigens, Neoplasm
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Receptors, Antigen, T-Cell
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Receptors, Chimeric Antigen