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Image Search Results
Journal: Molecular Therapy Oncolytics
Article Title: Characterization of a novel OX40 ligand and CD40 ligand-expressing oncolytic adenovirus used in the PeptiCRAd cancer vaccine platform
doi: 10.1016/j.omto.2021.02.006
Figure Lengend Snippet: Novel VALO-D102 oncolytic adenovirus produces high levels of biologically active human CD40 ligand (CD40L) and OX40 ligand (OX40L) (A) Schematic representation of genetic modifications in VALO-D102. The virus has a 24-base pair deletion in E1A; the CR1-alpha and gp19K genes in the E3A region have been replaced with human OX40L and CD40L genes; the 14.7K gene in the E3B region has been deleted; and finally, the adenovirus 5 knob domain has been replaced with the knob domain from adenovirus serotype 3. (B) A549 cells were infected with VALO-D102 at a MOI of 10. 72 h postinfection, supernatant was collected and added to a culture of Ramos-Blue reporter cells, and CD40 receptor activation by functional virus-produced CD40L was measured. (C) A549 cells were infected with VALO-D102 at a MOI of 10. 48 h postinfection, HEK293-OX40/NF-κB reporter cells were added to the infected A549 cells for 6 h, and OX40 activation by virus-expressed, functional membrane-bound OX40L was measured.
Article Snippet:
Techniques: Infection, Activation Assay, Functional Assay, Produced
Journal: Molecular Therapy Oncolytics
Article Title: Characterization of a novel OX40 ligand and CD40 ligand-expressing oncolytic adenovirus used in the PeptiCRAd cancer vaccine platform
doi: 10.1016/j.omto.2021.02.006
Figure Lengend Snippet: Virus-encoded OX40L and CD40L improve anti-tumor efficacy and induce robust infiltration of tumor-specific CD8 + T cells into the tumor in a syngeneic mouse model of B16.OVA melanoma (A) 1 × 10 9 VP of PeptiCRAd Ad5/3-D24-OVA or PeptiCRAd VALO-mD901-OVA was given intratumorally 6, 8, and 20 days post-tumor implantation. Average tumor growth curves for all treatment groups are shown. (B) Immunological analysis of tumors and tumor-draining lymph nodes of treated mice. Lymph nodes from all mice from each treatment group were pooled in order to get enough cells for the flow cytometric analysis. The number of mice in the mock group was 7 and in both PeptiCRAd groups, was 10. Statistical analysis was performed with one-way ANOVA. ∗p < 0.05, ∗∗p < 0.01.
Article Snippet:
Techniques: Tumor Implantation