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T-cell immunotherapy: looking forward.

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TLDR
The T Cell Immunotherapy: Optimizing T-cell trial design workshop as discussed by the authors was a workshop sponsored by the National Institutes of Health's Office of Biotechnology Activities (OBA), which brought together researchers to discuss the scientific advances and share new data on key trial design issues.
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This article is published in Molecular Therapy.The article was published on 2014-09-01 and is currently open access. It has received 58 citations till now. The article focuses on the topics: Population.

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Enhancing T cell therapy through TCR-signaling-responsive nanoparticle drug delivery

TL;DR: In this article, protein nanogels (NGs) were used to carry an interleukin-15 super-agonist complex, which selectively released these cargos in response to T cell receptor activation.
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Adoptive cellular therapy: a race to the finish line.

TL;DR: Some of the challenges—such as regulatory, cost, and manufacturing—and opportunities, including personalized gene-modified T cells, that face the field of adoptive cellular therapy are discussed.
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CD19-targeted CAR T-cell therapeutics for hematologic malignancies: interpreting clinical outcomes to date.

TL;DR: Clinical results reflecting the investigational use of CD19-targeted CAR T-cell therapeutics in patients with B-cell hematologic malignancies are reviewed, in light of differences in CAR design and production, and the limitations inherent in comparing outcomes between studies are outlined.
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Advantages and applications of CAR-expressing natural killer cells.

TL;DR: This review summarizes the data on CAR expressing NK cells focusing on the possible advantage using these short-lived effector cells and discusses the necessity of suicide switches.
References
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HLH-2004: Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis.

TL;DR: HLH‐2004 chemo‐immunotherapy includes etoposide, dexamethasone, cyclosporine A upfront and, in selected patients, intrathecal therapy with methotrexate and corticosteroids, and subsequent hematopoietic stem cell transplantation is recommended for patients with familial disease or molecular diagnosis, and patients with severe and persistent, or reactivated, disease.
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Chimeric Antigen Receptor–Modified T Cells in Chronic Lymphoid Leukemia

TL;DR: A low dose of autologous chimeric antigen receptor-modified T cells reinfused into a patient with refractory chronic lymphocytic leukemia expanded to a level that was more than 1000 times as high as the initial engraftment level in vivo, with delayed development of the tumor lysis syndrome and with complete remission.
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T Cells with Chimeric Antigen Receptors Have Potent Antitumor Effects and Can Establish Memory in Patients with Advanced Leukemia

TL;DR: It is reported that CAR T cells that target CD19 and contain a costimulatory domain from CD137 and the T cell receptor ζ chain have potent non–cross-resistant clinical activity after infusion in three of three patients treated with advanced chronic lymphocytic leukemia (CLL).
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