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BioWorld - Sunday, December 28, 2025
Home » Topics » Drugs » Immuno-oncology

Immuno-oncology
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Malignant B-cell lymphocytes seen in Burkitt lymphoma, stained with hematoxylin and eosin (H&E) stain.
Immuno-oncology

Gp350‑targeted CAR T-cell therapy exhibits preclinical efficacy in EBV-positive Burkitt lymphoma

Feb. 27, 2025
Epstein-Barr virus (EBV), a member of the herpesvirus family, is a highly common human pathogen that can remain latent in B lymphocytes after the primary infection. Although this latent state is frequently asymptomatic, in some cases, it can lead to the development of malignancies such as Burkitt lymphoma, Hodgkin lymphoma, nasopharyngeal carcinoma, and some gastric cancer subtypes.
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3D illustration of T cells fighting cancer
Immuno-oncology

Medigene and Epimab to codevelop TCR-guided T-cell engagers

Feb. 27, 2025
Medigene AG and Epimab Biotherapeutics Inc. have entered a strategic codevelopment agreement to research and develop off-the-shelf T-cell receptor (TCR)-guided T-cell engagers (TCR-TCEs) for the treatment of immune-related disorders, such as solid tumors.
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Illustration of cancer tumor
Immuno-oncology

Anti-TIGIT/PVRIG bispecific antibody has antitumor activity

Feb. 25, 2025
Although immune checkpoint inhibitors have shown noticeable clinical benefits, tumor evasion of single-agent immunotherapy occurs in some patients due to the compensatory role of alternative immune checkpoints. A viable strategy could be the use of combination immunotherapies targeting multiple immunosuppressive pathways to fully activate T cells and enhance response rates.
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Immuno-oncology

Targeting BPTF boosts NK cell immunotherapy in liver cancer

Feb. 25, 2025
Enhanced quantity and functionality of natural killer (NK) cells in hepatocellular carcinoma (HCC) have been associated with improved prognosis and survival. Therefore, NK cell-based immunotherapy has been proposed for treating HCC, relying on the activation of NK cell receptors like natural cytotoxicity receptors (NCRs), which recognize specific ligands on HCC cells. However, the effectiveness of this approach remains low due to tumor immune evasion.
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Non-Hodgkin lymphoma cells in the blood flow
Immuno-oncology

LTZ Therapeutics’ myeloid engager gains IND clearance

Feb. 25, 2025
LTZ Therapeutics Inc. has gained IND approval from the FDA for LTZ-301, a first-in-class myeloid engager immunotherapy intended to treat relapsed or refractory non-Hodgkin lymphoma (r/r NHL).
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Immuno-oncology

Ilab patents new PD-1/PD-L1 interaction inhibitors

Feb. 25, 2025
Ilab Co. Ltd. has disclosed programmed cell death 1 (PDCD1; PD-1; CD279)/PD-1 ligand 1 (PD-L1; CD274) interaction inhibitors reported to be useful for the treatment of cancer.
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Immuno-oncology

Adcentrx patents new antibody-drug conjugates

Feb. 21, 2025
Adcentrx Therapeutics Inc. and Adcentrx Therapeutics Shanghai Co. Ltd. have disclosed antibody-drug conjugates comprising a monoclonal antibody covalently bound to a cytotoxic drug through a linker.
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Art concept for vaccine for cancer
Immuno-oncology

IO-112 modulates tumor macrophages, allows control of tumor microenvironment

Feb. 20, 2025
Io Biotech Aps has presented preclinical data regarding their Arg1-derived peptide cancer vaccine IO-112 as a potential immunotherapeutic that would allow controlling the tumor microenvironment.
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Bispecific antibodies with heavy chain in green and pink, light chain in blue and yellow
Immuno-oncology

BA-4415, an anti-PD-L1/CD40 bispecific antibody for cancer immunotherapy

Feb. 20, 2025
Researchers from Tianjin University have published data regarding development and preclinical characterization of a new anti-PD-L1/CD40 bispecific antibody (BsAb), BA-4415, designed to activate CD40 signaling specifically in the context of PD-L1 while simultaneously blocking PD-1/PD-L1 signaling.
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Immuno-oncology

Epitopea and MSD collaborate to discover tumor-specific antigens for solid tumor

Feb. 20, 2025
Epitopea Ltd. has signed a license and research collaboration agreement with MSD (Merck & Co. Inc.) to identify Cryptigen tumor-specific antigens in an undisclosed solid tumor. Cryptigen TSAs are shared, nonmutated, aberrantly expressed antigens that are derived from what were thought to be noncoding regions of the genome.
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