Scientific Reports · 2019 · 117 citations · 43 references
MedicineHematologyOncologyCell TherapyHematologic OncologyImmunotherapyCancer ImmunotherapyCell-based ImmunotherapyCellular TherapyChemotherapy In Hematologic MalignanciesHematologic Malignancy TherapyNatural Killer Cell TherapyAcute Lymphoblastic Leukemia TreatmentCar-nk Cell TherapyChimeric Antigen Receptor T-cell Therapy ToxicityChronic Lymphocytic Leukemia TherapyCord Blood CellsHematologic Malignancy Car T-cell TherapyHematologic Malignancy Cell TherapyUmbilical Cord Blood Natural Killer Cells
Among hematological cancers, Acute Lymphoblastic Leukemia (ALL) and Chronic Lymphocytic Leukemia (CLL) are the most common leukemia in children and elderly people respectively. Some patients do not respond to chemotherapy treatments and it is necessary to complement it with immunotherapy-based treatments such as chimeric antigen receptor (CAR) therapy, which is one of the newest and more effective treatments against these cancers and B-cell lymphoma. Although complete remission results are promising, CAR T cell therapy presents still some risks for the patients, including cytokine release syndrome (CRS) and neurotoxicity. We proposed a different immune cell source for CAR therapy that might prevent these side effects while efficiently targeting malignant cells. NK cells from different sources are a promising vehicle for CAR therapy, as they do not cause graft versus host disease (GvHD) in allogenic therapies and they are prompt to attack cancer cells without prior sensitization. We studied the efficacy of NK cells from adult peripheral blood (AB) and umbilical cord blood (CB) against different target cells in order to determine the best source for CAR therapy. AB CAR-NK cells are slightly better at killing CD19 presenting target cells and CB NK cells are easier to stimulate and they have more stable number from donor to donor. We conclude that CAR-NK cells from both sources have their advantages to be an alternative and safer candidate for CAR therapy.
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Induction of Pluripotent Stem Cells from Adult Human Fibroblasts by Defined Factors
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CD19 CAR–T cells of defined CD4+:CD8+ composition in adult B cell ALL patients
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Medicine, Immunology, Oncology +17