| Vol. 21.36 – 19 October, 2020 |
| |
|
|
| 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] |
|
|
|
| PUBLICATIONSRanked by the impact factor of the journal |
|
|
|
| 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] |
|
|
|
| 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] |
|
|
|
| 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] |
|
|
|
| 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] |
|
|
|
| Researchers optimized a culturing protocol capable of efficiently generating small human cerebral organoids derived from hESCs and hiPSCs. [Molecular Psychiatry] |
|
|
|
| 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] |
|
|
|
| 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] |
|
|
|
| 43 subjects with B-cell acute lymphoblastic leukemia relapsing post allotransplant received CAR-T cells were analyzed. [Leukemia] |
|
|
|
| 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] |
|
|
|
| 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] |
|
|
|
| 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] |
|
|
|
|
| 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] |
|
|
|
| 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] |
|
|
|
|
| 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.)] |
|
|
|
| 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.] |
|
|
|
| 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.] |
|
|
|
|
| January 25 – January 27, 2021 Virtual |
|
|
|
|
|
| H. Lee Moffitt Cancer Center & Research Institute – Tampa, Florida, United States |
|
|
|
| University of Luxembourg- Luxembourg, Luxembourg |
|
|
|
| Terasaki Research Institute – Los Angeles, California, United States |
|
|
|
| GlaxoSmithKline – Stevenage, United Kingdom |
|
|
|
| Nanyang Technological University – Singapore, Singapore |
|
|
|
|