VNAR-based CAR-T cells targeting PD-L1
Construct PatternVNAR-based CAR-T cells targeting PD-L1 demonstrated strong anti-tumor effects in preclinical assays
Browse the toolkit beneath workflows. The mechanism branch runs mechanism -> architecture -> component, while the technique branch runs from high-level approaches down to concrete methods.
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Mechanism Branch
Layer 1
Mechanisms
Top-level concepts: biophysical action modes such as heterodimerization, photocleavage, or RNA binding.
Layer 2
Architectures
Arrangements that realize or deploy mechanisms, including switches, construct patterns, and delivery strategies.
Layer 3
Components
Low-level parts and sequence-defined elements used inside architectures, including protein domains and RNA elements.
Technique Branch
Layer 1
Approaches
High-level engineering practices such as computational design, directed evolution, sequence verification, and functional assay.
Layer 2
Methods
Concrete methods used to design, build, verify, or characterize engineered systems.
Showing 1-5 of 5
VNAR-based CAR-T cells targeting PD-L1 demonstrated strong anti-tumor effects in preclinical assays
Explicitly named in the anchor review as an autologous gp350-targeted CAR-T product in clinical development for EBV-positive lymphomas. High-priority EBV antiviral/oncovirology target with direct CAR-T relevance.
To achieve this, we engineered CD4+ T cells with chimeric antigen receptors (CARs) targeting fibrillar forms of aggregated amyloid-b2... we established the feasibility of amyloid plaque-specific CAR-T cells as a potential therapeutic avenue for AD.
CAR-NK cell therapy, as an emerging immunotherapeutic approach, has demonstrated significant potential. CAR-NK cells recognize and eliminate tumor cells through chimeric antigen receptors (CARs).
Exposure of HCC ectopically expressing GPC3+ to CAR-GPC3-IL15 and CAR-GPC3-IL15-IFNα NK cells demonstrated significant in vitro cytotoxicity and cytokine production, dependent on GPC3 expression.