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BioWorld - Sunday, December 7, 2025
Home » Topics » CAR T, BioWorld Science

CAR T, BioWorld Science
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CAR T cell with implanted gene strand
Immuno-oncology

Novel CAR strategies, arming the utility knife

Aug. 4, 2023
By Mar de Miguel
CAR T-cell immunotherapy is designed with different targets depending on the receptors they will bind to. CARs can also contain different tools, like the concept of a Swiss army knife, with several utensils for different tasks. The goal is to make them more effective and durable. During the second session of the Spotlight on Immuno-Oncology conference, “Novel CAR designs and approaches,” Robbie Majzner, of Stanford University, described expanding the main components of CAR T cells to acquire new functions and act on different cell pathways.
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3D rendering of CAR T therapy in cell
Immuno-oncology

At first ASGCT Immuno-oncology meeting, ways to build better T cells

Aug. 3, 2023
By Mar de Miguel
“From such a stick, such a splinter,” is a popular Spanish saying to explain how a son resembles his father. Like father, like son. The first Spotlight on Immuno-Oncology conference of the American Society of Gene & Cell Therapy (ASGCT) is the splinter of the ASGCT annual meeting, which brought together a group of experts in this field. It took place on Aug. 1 and 2, 2023, starting with a series of talks on “B Cell Malignancies and Beyond.”
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Acute myeloid leukemia
Immuno-oncology

Avencell’s CRISPR-engineered switchable allogeneic CAR T AVC-201 receives European trial clearance

July 25, 2023
Avencell Therapeutics Inc. has received approval from the EMA for its clinical trial application (CTA) for AVC-201 for the treatment of relapsed/refractory acute myeloid leukemia (AML) and other selected hematologic malignancies positive for CD123. A phase I study will be conducted in Germany.
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3D illustration demonstrating CAR T therapy
Cancer

CAR T cells that persist after treatment with leukemia develop a genetic mark

July 14, 2023
By Mar de Miguel
After CAR T-cell immunotherapy for leukemia, some children have a longer remission because the engineered cells remain active and control or prevent the growth of new tumor cells. A new collaborative study has found that these persistent cells expressed certain genes that could be identified through a transcriptional signature. The finding could explain why the treatment does not work in some patients, and potentially help to improve it, reducing relapses.
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T cells attacking cancer cells
Immuno-oncology

Maxcyte and Vittoria Biotherapeutics sign platform license agreement to support Vittoria’s cellular therapies

July 11, 2023
Maxcyte Inc. and Vittoria Biotherapeutics Inc. have signed a strategic platform license agreement for use of Maxcyte’s Flow Electroporation technology and Expert platform by Vittoria Biotherapeutics. Under the agreement, Vittoria will obtain nonexclusive clinical and commercial rights to use Maxcyte’s Flow Electroporation technology and Expert platform, and will pay Maxcyte platform licensing fees and program-related revenue.
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Malignant B-cell lymphocytes seen in Burkitt lymphoma, stained with hematoxylin and eosin (H&E) stain.
Immuno-oncology

Poseida to advance allogeneic dual CAR T therapy targeting CD19 and CD20 for B-cell malignancies

July 6, 2023
Poseida Therapeutics Inc. has received FDA clearance of its IND application for P-CD19CD20-ALLO1, an allogeneic dual chimeric antigen receptor (CAR) T-cell product candidate being developed for relapsed or refractory B-cell malignancies in partnership with F. Hoffmann-La Roche Ltd. The company is actively focused on opening clinical sites for a phase I study in adults with relapsed or refractory B-cell malignancies.
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Immuno-oncology

Coimmune exercises option to target DLL3 with IL-18 armored CAR technology under MSK agreement

June 28, 2023
Coimmune Inc. has obtained a license to target delta-like ligand 3 (DLL3) with IL-18 armored chimeric antigen receptor (CAR) technology. The company exercised an option to obtain an exclusive license in the DLL3-targeted, allogeneic CAR-cytokine induced killer (CAR-CIK) cell therapy field to IL-18 armored CAR technology under an agreement with Memorial Sloan Kettering Cancer Center (MSK).
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Photomicrograph of diffuse large B-cell lymphoma
Immuno-oncology

Panbela enters sponsored research agreement to explore polyamines for immune modulation in hematologic malignancies

June 14, 2023
Panbela Therapeutics Inc. has entered into a sponsored research agreement with The University of Texas MD Anderson Cancer Center for the evaluation of polyamine metabolic inhibitor...
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Illustration of bones showing difference in Ewing sarcoma, osteosarcoma and chondrosarcoma
Immuno-oncology

Cancervax’s UCLA research team creates monoclonal antibody candidates for Ewing sarcoma

June 13, 2023
Cancervax Inc. has announced further progress made by its research team at the University of California, Los Angeles (UCLA) toward...
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Immuno-oncology

EHA 2023: IF they work, logic-gated CAR T cells could work BETTER for complex targeting

June 13, 2023
By Anette Breindl
Part of the reason for CAR T cells’ astonishing success in B-cell cancers is that B cells are astonishingly easy to replace. CAR T cells are specific, yes. But they are not specific to tumor cells. They are specific to their target antigens. In the case of Yescarta (axicabtagene ciloleucel, Gilead Sciences Inc.) and Kymriah (tisagenlecleucel, Novartis AG), the first two clinically approved T cells, that target is CD19, which is expressed on B-cell precursors. And when it is successful, the treatment leaves patients without any B cells at all.
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