Cell Therapy News Volume 21.36 | Oct 19 2020

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    CTN 21.36 | Oct 19 2020


    Cell Therapy News by STEMCELL Technologies
    Vol. 21.36 – 19 October, 2020
    TOP STORY

    Microglia-Organized Scar-Free Spinal Cord Repair in Neonatal Mice

    Scientists transplanted either neonatal microglia or adult microglia treated with peptidase inhibitors into spinal cord lesions of adult mice, and found that both types of microglia significantly improved healing and axon regrowth.
    [Nature]

    Abstract

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    PUBLICATIONSRanked by the impact factor of the journal

    Anti-GD2
    CAR-NKT Cells in Patients with Relapsed or Refractory Neuroblastoma: An Interim Analysis

    Investigators report interim results from all three patients enrolled on dose level 1 in a Phase I dose-escalation trial of autologous natural killer T cells engineered to co-express a GD2-specific chimeric antigen receptor with interleukin-15 in children with relapsed or resistant neuroblastoma.
    [Nature Medicine]

    Abstract

    Systemic
    Anti–PD-1 Immunotherapy Results in PD-1 Blockade on T Cells in the Cerebrospinal Fluid

    Scientists evaluated pembrolizumab concentrations and PD-1 blockade on T cells in the cerebrospinal fluid after intravenous administration. Cerebrospinal fluid and blood samples were collected from ten adult patients with high-grade gliomas who were participating in clinical trials of intracranially administered chimeric antigen receptor T cells and intravenous pembrolizumab.
    [JAMA Oncology]

    Full Article

    Transplantation
    of hPSC-Derived Pericyte-Like Cells Promotes Functional Recovery in Ischemic Stroke Mice

    The authors generated pericyte-like cells (PCs) from human (h)PSCs through the intermediate stage of the cranial neural crest (CNC) and revealed that the hPSC-CNC PCs expressed typical pericyte markers including PDGFRβ, CD146, NG2, CD13, Caldesmon, and Vimentin, and displayed distinct contractile properties, vasculogenic potential and endothelial barrier function.
    [Nature Communications]

    Full Article

    In Vivo
    CRISPR/Cas9 Targeting of Fusion Oncogenes for Selective Elimination of Cancer Cells

    Investigators devised a simple, efficient and non-patient-specific gene-editing strategy through targeting of two introns of the genes involved in the rearrangement, allowing for robust disruption of the fusion oncogenes specifically in cancer cells.
    [Nature Communications]

    Full ArticlePress Release

    Human
    Cerebral Organoids Establish Subcortical Projections in the Mouse Brain after Transplantation

    Researchers optimized a culturing protocol capable of efficiently generating small human cerebral organoids derived from hESCs and hiPSCs.
    [Molecular Psychiatry]

    Full Article

    CD19-Specific
    CAR-T Cells that Express a PD-1/CD28 Chimeric Switch-Receptor is Effective in Patients with PD-L1 Positive B-Cell Lymphoma

    Scientists generated a novel anti-CD19 CAR expressing PD-1/CD28 chimeric switch-receptor. They then conducted a Phase Ib study to evaluate safety and efficacy of CD19-PD-1/CD28-CAR T cells in the treatment of PD-L1+ B-cell lymphoma.
    [Clinical Cancer Research]

    Abstract

    Treatment
    of Multiple Myeloma Using Chimeric Antigen Receptor T Cells with Dual Specificity

    The authors developed a ‘dual-CAR’ targeting two multiple myeloma-associated antigens and explored its safety and efficacy. To reduce the “off target” toxicity, they used the recognition of paired antigens that were co-expressed by the tumor, to induce efficient CAR T cell activation.
    [Cancer Immunology Research]

    Abstract

    Donor-Derived
    CD19 CAR-T Cell Therapy of Relapse of CD19-Positive B-ALL Post Allotransplant

    43 subjects with B-cell acute lymphoblastic leukemia relapsing post allotransplant received CAR-T cells were analyzed.
    [Leukemia]

    Full Article

    Melphalan
    and Exportin 1 Inhibitors Exert Synergistic Anti-Tumor Effects in Preclinical Models of Human Multiple Myeloma

    Multiple myeloma (MM) cells from newly diagnosed and relapsed/refractory MM patients were also sensitized by XPO1i to melphalan. In NOD/SCID-γ mice challenged with either parental 8226 or U266 MM and melphalan-resistant MM tumors, XPO1i/melphalan combination treatments demonstrated stronger synergistic anti-tumor effects than single-agent melphalan with minimal toxicity.
    [Cancer Research]

    Abstract

    Multiscale
    Fluorescent Tracking of Immune Cells in the Liver with a Highly Biocompatible Far-Red Emitting Polymer Probe

    A newly-designed water-soluble far-red emitting polymer probe, 19K-6H, with a large Stokes shift, was thus evaluated for the tracking of primary immune CD8 T cells. 19K-6H-labelled primary CD8 T cells were injected to mice in a classical model of immune mediated hepatitis.
    [Scientific Reports]

    Full Article

    Engineered
    AAV8 Capsid Acquires Heparin and AVB Sepharose Binding Capacity but Has Altered In Vivo Transduction Efficiency

    In vivo comparison by intramuscular, intravenous, and intraperitoneal vector administration demonstrated a significant decrease in adeno-associated virus 8-AVB-heparan sulfate transduction efficiency without alteration of the transduction profile.
    [Gene Therapy]

    Abstract

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    REVIEWS

    Overview of Current Targeted Therapy in Gallbladder Cancer

    The authors primarily focus on the targeted therapy capable of specifically inhibiting individual key molecules that govern aberrant signaling cascades in gallbladder cancer (GBC). Global clinical trials of targeted therapy in GBC are updated and may offer great value for novel pathologic and therapeutic insights of this deadly disease, ultimately improving the efficacy of treatment.
    [Signal Transduction and Targeted Therapy]

    Full Article

    Gene
    Therapy and Gene Correction: Targets, Progress, and Challenges for Treating Human Diseases

    Gene correction using CRISPR-Cas9 is an extension of gene therapy that has received considerable attention in recent years and boasts many possible uses beyond classical gene therapy approaches.
    [Gene Therapy]

    Abstract

    INDUSTRY AND POLICY NEWS

    XenoTherapeutics Granted US Patent Covering Method of Producing Clinically Acceptable Porcine Cells, Tissues, and Organs for Human Xenotransplantation

    XenoTherapeutics announced that the US Patent and Trademark Office has granted US Patent No. 10,799,614 to XenoTherapeutics, the patent covering methods for producing live-cell biological products from source animal donors for human xenotransplantation.
    [XenoTherapeutics (GlobeNewswire, Inc.)]

    Press Release

    Allogene
    Therapeutics and MD Anderson Announce Strategic Collaboration to Accelerate Advancement of Allogeneic CAR T Therapy (AlloCAR Tâ„¢)

    Allogene Therapeutics, Inc. and the University of Texas MD Anderson Cancer Center announced a strategic five-year collaboration agreement for the preclinical and clinical investigation of AlloCAR T candidates across Allogene’s broad portfolio of hematologic and solid tumors.
    [Allogene Therapeutics, Inc.]

    Press Release

    Precision BioSciences Announces US Patent Trial and Appeal Board Upholds Allogeneic CAR T Patents

    Precision BioSciences, Inc. announced that the US Patent and Trademark Office’s Patent Trial and Appeal Board has ruled in favor of Precision BioSciences in two patent interference proceedings that challenged nine US patents owned by Precision.
    [Precision BioSciences, Inc.]

    Press Release

    FEATURED EVENT

    Keystone
    Symposia: Emerging Cell Therapies: Realizing the Vision of NextGen Cell Therapeutics

    January 25 – January 27, 2021
    Virtual


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    JOB OPPORTUNITIES

    Postdoctoral Fellow – Cancer Immunology and Immunotherapy

    H. Lee Moffitt Cancer Center & Research Institute – Tampa, Florida, United States


    Postdoctoral Researcher – Translational Neuroscience

    University of Luxembourg- Luxembourg, Luxembourg

    Research
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    Terasaki Research Institute – Los Angeles, California, United States

    Vice
    President – Oncology and Cell Therapy

    GlaxoSmithKline – Stevenage, United Kingdom

    Research
    Fellow Position – Neural Cell Therapy

    Nanyang Technological University – Singapore, Singapore

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