| Vol. 13.00 – 8 January, 2021 |
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| Using high-throughput flow cytometry screening, single-cell RNA sequencing and CRISPR–Cas9-based cell-specific in vivo genetic perturbations in mice, researchers identified a subset of astrocytes that expressed the lysosomal protein LAMP12 and the death receptor ligand TRAIL. [Nature] |
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| PUBLICATIONSRanked by the impact factor of the journal |
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| Researchers showed that expression of the Epstein–Barr virus signaling protein LMP1 in B cells provoked T cell responses to multiple tumor-associated antigens. [Nature] |
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| The authors identified the SOX4 transcription factor as an important resistance mechanism to T cell-mediated cytotoxicity for triple negative breast cancer cells. [Cancer Cell] |
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| Scientists found that conventional dendritic cells, defined in mice via expression of the transcription factor Zbtb46, were a major source of circulating sIL-6R and, thus, systemically regulated IL-6 signaling. [Immunity] |
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| Intravascular cell labeling, cell transplantation, and fate-mapping studies established that classical CD14+ blood monocytes derived from ematopoietic stem and progenitor cells migrated into lung tissue and gave rise to human interstitial and alveolar macrophages. [Immunity] |
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| Scientists revealed that cytosolic lipopolysaccharide sensing triggered the release of galectin-1, a β-galactoside-binding lectin. They also found increased galectin-1 in sera from human patients with sepsis. [Nature Immunology] |
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| In vitro, although CD8+ T cells experiencing continuous stimulation or hypoxia alone differentiated into functional effectors, the combination rapidly drove T cell dysfunction consistent with exhaustion. [Nature Immunology] |
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| Investigators present a second-generation CD122-biased interleukin-2 (IL-2), developed by splitting and permanently grafting unmutated human IL-2 (hIL-2) to its antigen-binding groove on the anti-hIL-2 monoclonal antibody NARA1, thereby generating NARA1leukin. [Nature Communications] |
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| Scientists developed a new therapeutic strategy to switch macrophages phenotype and reactivate their anti-tumoral functions. They showed a dual activity of a proprotein convertases inhibitor as anti-glioma drug and anti-tumoral macrophages’ reactivation drug. [Cancer Gene Therapy] |
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| Researchers investigated the role of miR-199a-5p in T helper 17 (Th17) differentiation and determined whether extracellular vesicles derived from miR-199a-5p-modified adipose-derived MSCs could relieve immune thrombocytopenia by inhibiting Th17 differentiation. [Laboratory Investigation] |
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| The authors review the role of NAD+ and NAMPT in the ways that they may influence cancer metabolism, the immune system, stemness, aging, and cancer. They also review some ongoing research on therapeutic approaches. [Signal Transduction and Targeted Therapy] |
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| Scientists reveal the development of a highly promising therapeutic approach for cancer immunotherapy by targeting PD-1/PD-L1 ubiquitination. [Molecular Therapy] |
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| Genentech announced that tiragolumab, a novel cancer immunotherapy designed to bind to TIGIT, has been granted Breakthrough Therapy Designation by the FDA, in combination with Tecentriq® for the first-line treatment of people with metastatic non-small cell lung cancer whose tumors have high PD-L1 expression with no EGFR or ALK genomic tumor aberrations. [Genentech] |
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| January 25 – 28, 2021 Virtual |
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| University of Florida – Gainesville, Florida, United States |
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| Systimmune, Inc. – Redmond, Washington, United States |
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| Lerner Research Institute, Cleveland Clinic – Cleveland, Ohio, United States |
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| Salk Institute of Biological Studies – La Jolla, California, United States |
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| Salk Institute of Biological Studies – La Jolla, California, United States |
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