Abstract
Chimeric antigen receptor (CAR) T-cell therapy utilizes genetic engineering to redirect a patient's own T cells to target cancer cells. The remarkable results in hematological malignancies prompted investigating this approach in solid tumors such as pancreatic cancer. The complex tumor microenvironment, stromal hindrance in limiting immune response, and expression of checkpoint blockade on T cells pose hurdles. Herein, we summarize the opportunities, challenges, and state of knowledge in targeting pancreatic cancer with CAR T-cell therapy.
Keywords:
CAR T cells; adoptive cell therapy; checkpoint blockade; chimeric antigen receptor; immunotherapy.
© 2017 Wiley Periodicals, Inc.
MeSH terms
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Antigens, Neoplasm / immunology
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CD24 Antigen / immunology
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Carcinoembryonic Antigen / immunology
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Clinical Trials as Topic
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GPI-Linked Proteins / immunology
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Humans
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Immunotherapy, Adoptive*
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Mesothelin
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Mucin-1 / immunology
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Neoplasm Proteins / immunology
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Pancreatic Neoplasms / immunology*
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Pancreatic Neoplasms / therapy*
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Receptor, ErbB-2 / immunology
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Receptors, Antigen, T-Cell
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Receptors, Natural Killer Cell / immunology
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Stromal Cells / immunology
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T-Lymphocytes / immunology
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T-Lymphocytes / transplantation*
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Transplantation Conditioning
Substances
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Antigens, Neoplasm
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CD24 Antigen
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CD24 protein, human
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Carcinoembryonic Antigen
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GPI-Linked Proteins
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MUC1 protein, human
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Mucin-1
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Neoplasm Proteins
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PSCA protein, human
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Receptors, Antigen, T-Cell
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Receptors, Natural Killer Cell
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ERBB2 protein, human
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Receptor, ErbB-2
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Mesothelin