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CD8

An In Vivo Selection-Derived D-Peptide for Engineering Erythrocyte-Binding Antigens That Promote Immune Tolerance

[Proceedings of the National Academy of Sciences of the United States of America] Researchers investigated a straightforward approach based on erythrocyte binding to promote antigen-specific tolerance to both peptides and proteins, and showed that a fully D-chiral peptide library could be selected in vivo for the de novo discovery of a robust erythrocyte binder, which they attached to peptide and protein antigens.

Immunotherapy Combinations Overcome Resistance to Bispecific T Cell Engager Treatment in T Cell–Cold Solid Tumors

[Science Translational Medicine] Using an immunocompetent mouse model expressing a humanized CD3ε chain and bispecific T cell engager (BiTE) molecules directed against mouse CD19, mouse CLDN18.2, or human EPCAM antigens, researchers investigated the pharmacokinetic and pharmacodynamic parameters and immune correlates associated with BiTE efficacy across multiple syngeneic solid-tumor models.

IL-33 Activates mTORC1 and Modulates Glycolytic Metabolism in CD8+ T Cells

[Immunology] The authors found increased mouse IL-33 expression in CD8+ T cells following cell activation via anti-CD3/CD28 stimulation in vitro or Lymphocytic choriomeningitis virus (LCMV) infection in vivo.

Human Small Intestinal Infection by SARS-CoV-2 Is Characterized by a Mucosal Infiltration with Activated CD8+ T Cells

[Mucosal Immunology] Researchers indicated that intraepithelial CD8+ T cells were activated upon infection of intestinal epithelial cells with SARS-CoV-2, providing one possible explanation for gastrointestinal symptoms associated with COVID-19.

Gain-of-Function p53R172H Mutation Drives Accumulation of Neutrophils in Pancreatic Tumors, Promoting Resistance to Immunotherapy

[Cell Reports] Researchers compared the immune profiles generated by KrasG12D-mutated mouse pancreatic ductal epithelial cells engineered genetically to express the Trp53R172H mutation with their p53 wild-type control.

Pro-Inflammatory β Cell Small Extracellular Vesicles Induce β Cell Failure through Activation of the CXCL10/CXCR3 Axis in Diabetes

[Cell Reports] Scientists reported that pro-inflammatory β cell small extracellular vesicles induced β cell dysfunction, promoted a pro-inflammatory islet transcriptome, and enhanced recruitment of CD8+ T cells and macrophages.

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