 | Vol. 9.01 – 12 January, 2021 |
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| Scientists developed tessa, a tool to integrate T cell receptors (TCRs) with gene expression of T cells to estimate the effect that TCRs confer on the phenotypes of T cells. Tessa leveraged techniques combining single-cell RNA-sequencing with TCR sequencing. [Nature Methods] |
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 | PUBLICATIONSRanked by the impact factor of the journal |
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| Researchers examined the T cell-intrinsic role of Activin-A, a TGF-β superfamily member closely related to TGF-β1, in pathogenic Th17 cell differentiation. Activin-A expression was increased in individuals with relapsing-remitting multiple sclerosis and in mice with experimental autoimmune encephalomyelitis. [Immunity] |
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| The authors used full-length Smart-seq2 single-cell RNA-sequencing to unravel tissue-specific transcriptional profiles and heterogeneity of CD127+ ILCs across four human tissues. [Cell Research] |
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| Investigators showed that interleukin-2 (IL-2) acted as an environmental cue to induce CD8+ T cell exhaustion within tumor microenvironments. [Nature Immunology] |
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| Scientists report that CD8+ T-cell activation and anti-tumor responses were strongly potentiated by the non-essential amino acid Asn. Increased Asn levels enhanced CD8+ T-cell activation and effector functions against tumor cells in vitro and in vivo. [Nature Cell Biology] |
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| Researchers showed that Mitomycin C (MMC) promoted immunogenic cell death (ICD) and in vivo tumor protection. MMC-induced ICD relied on metabolic reprogramming of tumor cells toward increased oxidative phosphorylation. [Science Translational Medicine] |
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| The levels of infiltrating myeloid-derived suppressor cells (MDSCs) were significantly higher in the non-responding organoids and were selectively reduced in the responding group, with MDSCs showing increased apoptosis and attenuated functional activity after anti-PD-1 treatment. [Signal Transduction and Targeted Therapy] |
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| To target both B cell Non-Hodgkin’s lymphoma and follicular T helper cells in the tumor microenvironment, researchers applied a chimeric antigen receptor that recognized human CXCR5 with high avidity. [Nature Communications] |
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| Elevated expression of CD47 protected K562 tumor cells and mouse and human MHC class I–deficient target cells against SIRPα+ primary NK cells, but not against SIRPα– NKL or NK92 cells. SIRPα deficiency or antibody blockade increased the killing capacity of NK cells. [Journal of Experimental Medicine] |
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| Investigators showed that healthy donors and cancer patients harbor CD4+ and CD8+ T cells specific for TGFβ-derived epitopes and that cytotoxic T cells with specificity toward TGFβ-derived epitopes were able to recognize and kill cancer cell lines in a TGFβ-dependent manner. [Cellular & Molecular Immunology] |
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| Researchers investigated the expression level and biological function of angiomotin (AMOT) in diffuse large B-cell lymphoma (DLBCL). AMOT expression was significantly reduced in DLBCL biopsy section, and low AMOT expression was associated with poor clinical prognosis. [Cancer Gene Therapy] |
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| The authors provide a perspective on synergistic therapies that combine anti-TGFβ therapy with cytotoxic chemotherapy, targeted therapy, radiotherapy, or immunotherapy. [Signal Transduction and Targeted 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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| The University of Utah School of Medicine – Salt Lake City, Utah, United States |
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| Systimmune, Inc. – Redmond, Washington, United States |
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| University of Florida – Gainesville, Florida, United States |
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| University of Illinois at Chicago – Chicago, Illinois, United States |
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| Karolinska Institutet – Huddinge, Sweden |
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