Search Results - "Spencer, H. Trent"
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Targeting T cell malignancies using CAR-based immunotherapy: challenges and potential solutions
Published in Journal of hematology and oncology (29-12-2019)“…Chimeric antigen receptor (CAR) T cell therapy has been successful in treating B cell malignancies in clinical trials; however, fewer studies have evaluated…”
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A combined treatment regimen of MGMT-modified γδ T cells and temozolomide chemotherapy is effective against primary high grade gliomas
Published in Scientific reports (26-10-2021)“…Chemotherapeutic drugs such as the alkylating agent Temozolomide (TMZ), in addition to reducing tumor mass, can also sensitize tumors to immune recognition by…”
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Enhancing the pharmaceutical properties of protein drugs by ancestral sequence reconstruction
Published in Nature biotechnology (01-01-2017)“…The pharmaceutical properties of coagulation factor VIII are improved by reconstructing the protein's ancestral sequence. Optimization of a protein's…”
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4
Development of chimeric antigen receptors targeting T-cell malignancies using two structurally different anti-CD5 antigen binding domains in NK and CRISPR-edited T cell lines
Published in Oncoimmunology (04-03-2018)“…Relapsed T-cell malignancies have poor outcomes when treated with chemotherapy, but survival after allogeneic bone marrow transplantation (BMT) approaches 50%…”
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Transplanting FVIII/ET3-secreting cells in fetal sheep increases FVIII levels long-term without inducing immunity or toxicity
Published in Nature communications (14-07-2023)“…Hemophilia A is the most common X-linked bleeding disorder affecting more than half-a-million individuals worldwide. Persons with severe hemophilia A have…”
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Dissecting the cellular components of ex vivo γδ T cell expansions to optimize selection of potent cell therapy donors for neuroblastoma immunotherapy trials
Published in Oncoimmunology (31-12-2022)“…γδ T lymphocytes represent an emerging class of cellular immunotherapy with preclinical promise to treat cancer, notably neuroblastoma. The innate-like immune…”
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The Immune Response to the fVIII Gene Therapy in Preclinical Models
Published in Frontiers in immunology (15-04-2020)“…Neutralizing antibodies to factor VIII (fVIII), referred to as "inhibitors," remain the most challenging complication post-fVIII replacement therapy…”
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Engineered drug resistant γδ T cells kill glioblastoma cell lines during a chemotherapy challenge: a strategy for combining chemo- and immunotherapy
Published in PloS one (2013)“…Classical approaches to immunotherapy that show promise in some malignancies have generally been disappointing when applied to high-grade brain tumors such as…”
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Directing the migration of serum-free, ex vivo -expanded Vγ9Vδ2 T cells
Published in Frontiers in immunology (29-02-2024)“…Vγ9Vδ2 T cells represent a promising cancer therapy platform because the implementation of allogenic, off-the-shelf product candidates is possible. However,…”
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10
Comparison of different gene addition strategies to modify placental derived-mesenchymal stromal cells to produce FVIII
Published in Frontiers in immunology (15-12-2022)“…Placenta-derived mesenchymal cells (PLCs) endogenously produce FVIII, which makes them ideally suited for cell-based fVIII gene delivery. We have previously…”
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Ligand-based targeting of c-kit using engineered γδ T cells as a strategy for treating acute myeloid leukemia
Published in Frontiers in immunology (2023)“…The application of immunotherapies such as chimeric antigen receptor (CAR) T therapy or bi-specific T cell engager (BiTE) therapy to manage myeloid…”
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Structure of Blood Coagulation Factor VIII in Complex With an Anti-C2 Domain Non-Classical, Pathogenic Antibody Inhibitor
Published in Frontiers in immunology (10-06-2021)“…Factor VIII (fVIII) is a procoagulant protein that binds to activated factor IX (fIXa) on platelet surfaces to form the intrinsic tenase complex. Due to the…”
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Ex vivo expanded patient-derived γδ T-cell immunotherapy enhances neuroblastoma tumor regression in a murine model
Published in Oncoimmunology (2019)“…An effective therapy regimen for relapsed/refractory high-risk neuroblastoma (NB) includes the anti-GD2 monoclonal antibody, dinutuximab, in combination with…”
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Enhancing the effectiveness of γδ T cells by mRNA transfection of chimeric antigen receptors or bispecific T cell engagers
Published in Molecular therapy. Oncolytics (15-06-2023)“…Adoptive cell therapy (ACT) utilizing γδ T cells is becoming a promising option for the treatment of cancer, because it offers an off-the-shelf allogeneic…”
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Target-Cell-Directed Bioengineering Approaches for Gene Therapy of Hemophilia A
Published in Molecular therapy. Methods & clinical development (15-06-2018)“…Potency is a key optimization parameter for hemophilia A gene therapy product candidates. Optimization strategies include promoter engineering to increase…”
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Coagulation factor IX gene transfer to non-human primates using engineered AAV3 capsid and hepatic optimized expression cassette
Published in Molecular therapy. Methods & clinical development (10-12-2021)“…Hepatic gene transfer with adeno-associated viral (AAV) vectors shows much promise for the treatment of the X-linked bleeding disorder hemophilia B in multiple…”
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Phenotypic correction of hemophilia A in sheep by postnatal intraperitoneal transplantation of FVIII-expressing MSC
Published in Experimental hematology (01-12-2011)“…We recently re-established a line of sheep that accurately mimics the clinical symptoms and genetics of severe hemophilia A (HA). Here, we tested a novel,…”
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Non-genotoxic conditioning facilitates hematopoietic stem cell gene therapy for hemophilia A using bioengineered factor VIII
Published in Molecular therapy. Methods & clinical development (11-06-2021)“…Hematopoietic stem and progenitor cell (HSPC) lentiviral gene therapy is a promising strategy toward a lifelong cure for hemophilia A (HA). The primary risks…”
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Treatment of a solid tumor using engineered drug-resistant immunocompetent cells and cytotoxic chemotherapy
Published in Human gene therapy (01-07-2012)“…Multimodal therapy approaches, such as combining chemotherapy agents with cellular immunotherapy, suffers from potential drug-mediated toxicity to immune…”
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Directed Engineering of a High-expression Chimeric Transgene as a Strategy for Gene Therapy of Hemophilia A
Published in Molecular therapy (01-07-2009)“…Human coagulation factor VIII (fVIII) is inefficiently biosynthesized in vitro and has proven difficult to express at therapeutic levels using available…”
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