Fig. 4 Expression of cleaved caspase 3, PD-L1, and PD-1 in HGGs after reovirus treatment. Expression of cleaved caspase 3, PD-L1, and PD-1 in HGGs after.

Slides:



Advertisements
Similar presentations
Fig. 1 GBM TIMs expand to inhibit vaccine-induced T-cell mediated tumor cytolysis via PD-1/PD-L1 regulatory pathway. (A, D) CD163, DAPI, (B, E) PD-L1,
Advertisements

Anifrolumab inhibits cytokine production, plasmacytoid dendritic cell (pDC) activation and the type I (interferon gene signature) IFN gene signature. Anifrolumab.
Fig. 2. LUM015 fluorescently labels tumor cells in mouse models of STS and breast cancer. LUM015 fluorescently labels tumor cells in mouse models of STS.
Fig. 6. AZD6738 induces DNA damage and apoptosis and exhibits antitumor efficacy in xenograft models of high-risk medulloblastoma and neuroblastoma. AZD6738.
Human NK cell development in NOD/SCID mice receiving grafts of cord blood CD34+ cells by Christian P. Kalberer, Uwe Siegler, and Aleksandra Wodnar-Filipowicz.
Fig. 1. Potent and selective down-regulation of KRAS mRNA and protein by AZD4785 in vitro and in vivo. Potent and selective down-regulation of KRAS mRNA.
PD-1 and LAG-3 expression in MSI and MSS colorectal cancer specimens.
Fig. 5 Maraba induces antitumor T cell immunity.
Fig. 2. Engraftment of CART-EGFRvIII and cytokine modulation in the peripheral blood. Engraftment of CART-EGFRvIII and cytokine modulation in the peripheral.
Fig. 6. Combinatorial VCPI and OV M1 treatment is efficacious in vivo and ex vivo. Combinatorial VCPI and OV M1 treatment is efficacious in vivo and ex.
Fig. 4. aPD-1 mAb transfer to macrophages is mediated by FcγRs.
Fig. 1 Localized treatment of TNBC cancers kills tumor cells and minimizes the metastatic burden. Localized treatment of TNBC cancers kills tumor cells.
Fig. 2 TLR8 is aberrantly expressed on pDCs from SSc patients.
Fig. 6. N95BA5 biocompatibility beyond intended use frame.
Fig. 1 pDCs infiltrate the skin of SSc patients and spontaneously secrete IFN-α and CXCL4. pDCs infiltrate the skin of SSc patients and spontaneously secrete.
Fig. 8. mRIPO elicits neutrophil influx followed by DC and T cell infiltration into tumors. mRIPO elicits neutrophil influx followed by DC and T cell infiltration.
Fig. 3 TLR8 signaling induces CXCL4 and IFN-α secretion by SSc PDCs.
Maraba treatment sensitizes 4T1 tumors to immune checkpoint blockade
Fig. 7. The PD-L1 defect is evident in HSPCs from T1D patients.
Intravenous delivery of reovirus to primary and secondary brain tumors
Fig. 2. GPC3 expression in normal and tumor tissues.
Fig. 4. The effects of AVP or d(Leu4Lys8)VP, a specific AVPR1B agonist, on anemic rodents. The effects of AVP or d(Leu4Lys8)VP, a specific AVPR1B agonist,
Fig. 5. Immunohistochemistry of the tumor microenvironment in GBM specimens before and after CART-EGFRvIII infusion. Immunohistochemistry of the tumor.
Expression of CD36 and psap in a TMA of human ovarian cancer patients
Fig. 4. Antitumor efficacy of ERY974 against various cancer types.
Fig. 4 CXCL4 potentiates TLR8-mediated activation of SSc pDCs.
Kathleen R. Bartemes, BA, Gail M. Kephart, BS, Stephanie J
Fig. 5 Combination intravenous reovirus and checkpoint inhibition in an orthotopic syngeneic brain tumor model. Combination intravenous reovirus and checkpoint.
Fig. 2 In vitro assessment of hESC-RPE cell sheets.
Christian Möbs, Thomas Schmidt  Journal of Investigative Dermatology 
Fig. 3 In situ vaccination with CpG and anti-OX40 is therapeutic in a spontaneous tumor model. In situ vaccination with CpG and anti-OX40 is therapeutic.
Fig. 2. Circulating VEGF in GCA patients up-regulates microvascular endothelial Jagged1. Circulating VEGF in GCA patients up-regulates microvascular endothelial.
Fig. 5. Accelerated NASH-driven fibrogenesis in obese IFN-γ−/− mice is characterized by severe eosinophilic inflammation during TGF-β blockade. Accelerated.
Fig. 3. Genetically engineered PD-L1
Fig. 4. Genetically engineered PD-L1
Fig. 4. Irisin protected against oxidative stress and apoptosis in IR-injured lung tissue. Irisin protected against oxidative stress and apoptosis in IR-injured.
Fig. 1. PGBD5-expressing cells do not tolerate deficiency of nonhomologous end-joining DNA repair. PGBD5-expressing cells do not tolerate deficiency of.
Fig. 7 CSPG4-high GBMs show more microglia than CSPG4-low GBMs and express TNFα. CSPG4-high GBMs show more microglia than CSPG4-low GBMs and express TNFα.
Fig. 4 TNF-α up-regulates Fas/Fap-1 expression to promote IL-1RA–sEV release in murine MSCs. TNF-α up-regulates Fas/Fap-1 expression to promote IL-1RA–sEV.
Fig. 1 CpG induces the expression of OX40 on CD4 T cells.
Fig. 6. pKL cells revert hyperglycemia in NOD mice in vivo.
Fig. 7 DMN-Tre labeling of Mycobacterium tuberculosis is inhibited by tuberculosis drug cocktail, unlike auramine staining. DMN-Tre labeling of Mycobacterium.
Fig. 1 Effect of preinfection β7Hi CD45RA−CD4+ T cell frequency on HIV acquisition risk in CAPRISA 004 study. Effect of preinfection β7Hi CD45RA−CD4+ T.
PAAND is driven by local inflammasome activation and IL-1β production
CXCR5 expression accelerates Eμ-Tcl1 leukemogenesis and is indispensable for tumor cell recruitment to lymphoid B-cell follicles. CXCR5 expression accelerates.
Fig. 3. VEGFR-3 signaling increases infiltration of naïve T cells in a CCR7-dependent manner. VEGFR-3 signaling increases infiltration of naïve T cells.
Fig. 4 Surgery initiates a systemic inflammatory response that triggers the outgrowth of distant immunogenic tumors and can be inhibited by perioperative.
Fig. 1 CSPG4 is expressed in GBM specimens and GBM-NS and associated with more aggressive disease. CSPG4 is expressed in GBM specimens and GBM-NS and associated.
Selection of a 4-1BB-endodomain–based anti-EGFRvIII CAR construct
Fig. 3 CSF1 is expressed in human melanoma.
Fig. 5 DMN-Tre labeling is selective for live mycobacteria.
Fig. 1. Specificity of FolamiR uptake in cancer cells in culture.
Figure 3 Cytokine gene expression in PBMC stimulated with PPD or MBP in vitroCytokine messenger RNA transcripts were isolated from peripheral blood mononuclear.
Fig. 5 Treatment with an OX40 agonist antibody of 3-week-old HBVtgRag−/− mice or mice with chronic HBV disease results in an altered immune response to.
Fig. 1 LB100 and LB102 specifically inhibit PP2A phosphatase activity and the growth of BCR-ABL+ cells. LB100 and LB102 specifically inhibit PP2A phosphatase.
Correlation of reovirus RNA/protein with proliferating tumor cells
Fig. 6 Combination therapy with LVSOD2 and LVshCTGF preserves flap volume and reduces fibrosis after RT. Combination therapy with LVSOD2 and LVshCTGF preserves.
Caspase 8 is expressed in human ESCs but is not regulated by IFN-γ, TNF-α or hCG. Caspase 8 is expressed in human ESCs but is not regulated by IFN-γ, TNF-α.
Figure 2 Effect of DMF therapy on the T helper cell repertoire and cytokine production Effect of DMF therapy on the T helper cell repertoire and cytokine.
Correlations between two measures of type I interferon activity and serum galectin-3-binding protein in the SLE-IFN-α (n=26) and HC-IFN-α (n=10) cohorts.
Fig. 1. Potent and selective down-regulation of KRAS mRNA and protein by AZD4785 in vitro and in vivo. Potent and selective down-regulation of KRAS mRNA.
BMS blocks functional responses in primary immune cells driven by IFNα
Fig. 4. Long-term persistence of CTL019 cells and polyfunctionality in patients achieving CR. Long-term persistence of CTL019 cells and polyfunctionality.
Fig. 1 IDH3α expression is elevated in human-derived gliomas.
Increase in proliferation and activation of immune cells in peripheral blood after NKTR-214 treatment. Increase in proliferation and activation of immune.
Intratumoral changes in critical lymphocyte populations and numbers after NKTR-214 treatment. Intratumoral changes in critical lymphocyte populations and.
PD-1 and CD103 are coexpressed on CD8+ T cells but demonstrate distinct mechanisms of regulation. PD-1 and CD103 are coexpressed on CD8+ T cells but demonstrate.
Fig. 6. Combinatorial VCPI and OV M1 treatment is efficacious in vivo and ex vivo. Combinatorial VCPI and OV M1 treatment is efficacious in vivo and ex.
Fig. 3. Association between peak CTL019 expansion and response.
(A–E) demonstrate a kidney biopsy from a patient with lupus nephritis (LN) class V. Representative micrographs: (A), an inflammatory infiltrate with T.
Presentation transcript:

Fig. 4 Expression of cleaved caspase 3, PD-L1, and PD-1 in HGGs after reovirus treatment. Expression of cleaved caspase 3, PD-L1, and PD-1 in HGGs after reovirus treatment. (A) Representative trial and control patient HGG sections stained for cleaved caspase 3 (brown) by IHC. Scale bars, 60 μm. (B) Representative trial and control patient HGG sections stained by IHC for programmed death ligand 1 (PD-L1) (brown). Scale bars, 30 μm. (C) Representative (one of three samples tested) flow cytometry for PD-L1 on GBM tumor-infiltrating lymphocytes (TILs) (bottom) or peripheral blood mononuclear cells (PBMCs) (top) derived from the same patient, after stimulation for 48 hours using 1 plaque-forming unit per cell reovirus. PBS, phosphate-buffered saline; Ab, antibody. (D) Representative trial and control patient HGG sections stained by IHC for programmed cell death protein 1 (PD-1) (brown). Scale bars, 30 μm. (E) Representative flow cytometry for PD-L1 on GBM1 cells after stimulation with combinations of purified interferon (IFN)–α/IFN-β/IFN-γ for 24 hours, each at 100 pg/ml. (F) Representative flow cytometry for PD-L1 on GBM1 cells after stimulation with ex vivo HGG-derived conditioned medium (CM) or reovirus-conditioned medium (RCM) for 24 hours (at a concentration of 1:4 of CM to native medium). (G) Representative flow cytometry for PD-L1 on GBM1 cells after stimulation using PBMC-derived CM or RCM for 24 hours (at a concentration of 1:4 of CM to native medium) with blockade of IFN-α+β/γ/α+β+γ or equivalent isotype controls. Adel Samson et al., Sci Transl Med 2018;10:eaam7577 Published by AAAS