Search Results - "De Oliveira, Satiro"
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Acoustofluidic sonoporation for gene delivery to human hematopoietic stem and progenitor cells
Published in Proceedings of the National Academy of Sciences - PNAS (19-05-2020)“…Advances in gene editing are leading to new medical interventions where patients’ own cells are used for stem cell therapies and immunotherapies. One of the…”
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In Vitro Generation of Human NK Cells Expressing Chimeric Antigen Receptor Through Differentiation of Gene-Modified Hematopoietic Stem Cells
Published in Methods in molecular biology (Clifton, N.J.) (01-01-2016)“…NK cells represent a very promising source for adoptive cellular approaches for cancer immunotherapy, and extensive research has been conducted, including…”
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Antiviral cellular therapy for enhancing T-cell reconstitution before or after hematopoietic stem cell transplantation (ACES): a two-arm, open label phase II interventional trial of pediatric patients with risk factor assessment
Published in Nature communications (18-04-2024)“…Viral infections remain a major risk in immunocompromised pediatric patients, and virus-specific T cell (VST) therapy has been successful for treatment of…”
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A CD19/Fc fusion protein for detection of anti-CD19 chimeric antigen receptors
Published in Journal of translational medicine (29-01-2013)“…Chimeric Antigen Receptors (CARs) consist of the antigen-recognition portion of a monoclonal antibody fused to an intracellular signaling domain capable of…”
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Mediport use as an acceptable standard for CAR T cell infusion
Published in Frontiers in immunology (27-10-2023)“…Mediport use as a clinical option for the administration of chimeric antigen receptor T cell (CAR T cell) therapy in patients with B-cell malignancies has yet…”
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Pre-clinical development of gene modification of haematopoietic stem cells with chimeric antigen receptors for cancer immunotherapy
Published in Human vaccines & immunotherapeutics (04-05-2017)“…Patients with refractory or recurrent B-lineage hematologic malignancies have less than 50% of chance of cure despite intensive therapy and innovative…”
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Hematopoietic Stem-Cell Gene Therapy for Cerebral Adrenoleukodystrophy
Published in The New England journal of medicine (26-10-2017)“…Among boys with cerebral adrenoleukodystrophy, matched donors for allogeneic transplantation are available to only a few. Infusion of CD34+ autologous stem…”
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Use of Rapamycin in a Patient With Juvenile Myelomonocytic Leukemia: A Case Report
Published in JIM - high impact case reports (01-07-2017)“…The relapse rate for children with juvenile myelomonocytic leukemia (JMML) status post hematopoietic stem cell transplantation (HSCT) approaches 50% within 5…”
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Hematopoietic stem cells for cancer immunotherapy
Published in Immunological reviews (01-01-2014)“…Summary Hematopoietic stem cells (HSCs) provide an attractive target for immunotherapy of cancer and leukemia by the introduction of genes encoding T‐cell…”
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Site-Specific Gene Editing of Human Hematopoietic Stem Cells for X-Linked Hyper-IgM Syndrome
Published in Cell reports (Cambridge) (29-05-2018)“…X-linked hyper-immunoglobulin M (hyper-IgM) syndrome (XHIM) is a primary immunodeficiency due to mutations in CD40 ligand that affect immunoglobulin…”
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A Cetuximab-Mediated Suicide System in Chimeric Antigen Receptor-Modified Hematopoietic Stem Cells for Cancer Therapy
Published in Human gene therapy (01-04-2019)“…Using gene modification of hematopoietic stem cells (HSC) to create persistent generation of multilineage immune effectors to target cancer cells directly is…”
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HJV mutations causing hemochromatosis: variable phenotypic expression in a pair of twins
Published in Haematologica (Roma) (01-08-2024)Get full text
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Fluorinated Silane-Modified Filtroporation Devices Enable Gene Knockout in Human Hematopoietic Stem and Progenitor Cells
Published in ACS applied materials & interfaces (06-09-2023)“…Intracellular delivery technologies that are cost-effective, non-cytotoxic, efficient, and cargo-agnostic are needed to enable the manufacturing of cell-based…”
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Lentiviral Gene Therapy for Cerebral Adrenoleukodystrophy
Published in The New England journal of medicine (10-10-2024)“…Thirty-two patients with cerebral adrenoleukodystrophy received lentiviral gene therapy, and after a median of 6 years most were free of major disability…”
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Development of Hematopoietic Stem Cell-Engineered Invariant Natural Killer T Cell Therapy for Cancer
Published in Cell stem cell (03-10-2019)“…Invariant natural killer T (iNKT) cells are potent immune cells for targeting cancer; however, their clinical application has been hindered by their low…”
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Successful engraftment of haploidentical bone marrow with post‐transplantation cyclophosphamide in patients with aplastic anemia
Published in Pediatric transplantation (01-03-2020)“…Patients with severe aplastic anemia (SAA) may benefit from hematopoietic stem cell transplantation, but many of them lack a matched donor. Haploidentical…”
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Pediatric hematopoietic cell transplantation: Longitudinal trends in body mass index and outcomes
Published in Pediatric transplantation (01-11-2020)“…Pediatric recipients of HCT may have a high susceptibility for overweight and obesity, and obesity may negatively impact post‐transplant mortality and…”
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False-positive magnetic resonance imaging findings in follow-up of pediatric patients with tumors of the central nervous system
Published in SAGE open medical case reports (01-01-2016)“…Management of patients with central nervous system tumors relies largely on magnetic resonance imaging scans to document disease progression or recurrence. The…”
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Gene-modified hematopoietic stem cells for cancer immunotherapy
Published in Human vaccines & immunotherapeutics (28-04-2014)“…The rapid expansion of available cancer immunotherapies has resulted in favorable early outcomes. Specifically the use of gene therapy to introduce chimeric…”
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Same sibling marrow following cord allogeneic transplantation as therapy for second relapse acute promyelocytic leukemia in a pediatric patient
Published in Pediatric transplantation (01-03-2016)“…Optimal therapy for relapsed APL in pediatric patients is controversial. Allogeneic HSCT is an alternative, with event‐free survival of 70–75%. We report a…”
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