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CD8

An Engineered IL-2 Reprogrammed for Anti-Tumor Therapy Using a Semi-Synthetic Organism

[Nature Communications] The authors utilized an engineered microbial organism with a six-letter semi-synthetic DNA code to generate a library of site-specific, click chemistry compatible amino acid substitutions in the human cytokine IL-2.

Intercellular Crosstalk of Liver Sinusoidal Endothelial Cells in Liver Fibrosis, Cirrhosis and Hepatocellular Carcinoma

[Digestive and Liver Disease] Scientists summarize the current knowledge of how different crosstalk between liver sinusoidal endothelial cells and other liver cells, including hepatocytes, hepatic stellate cells, macrophoges, immune cells in liver and extra cellular matrix contribute to the physiological function and the progrssion from liver fibrosis to cirrhosis, or even to hepatocellular carcinoma.

The CD155/TIGIT Axis Promotes and Maintains Immune Evasion in Neoantigen-Expressing Pancreatic Cancer

[Cancer Cell] Using multiple preclinical models of neoantigen-expressing pancreatic adenocarcinoma (PDAC), scientists demonstrated that intratumoral neoantigen-specific CD8+ T cells adopted multiple states of dysfunction, resembling those in tumor-infiltrating lymphocytes of PDAC patients.

Significance of Bystander T Cell Activation in Microbial Infection

[Nature Immunology] The authors describe the history of research on bystander CD8+ T cell activation as well as evidence of bystander activation. They also discuss the mechanisms and immunopathological roles of bystander activation in various microbial infections.

Differentiation of Exhausted CD8+ T Cells after Termination of Chronic Antigen Stimulation Stops Short of Achieving Functional T Cell Memory

[Nature Immunology] Scientists confirmed pervasive phenotypic, functional and transcriptional differences between memory and exhausted antigen-specific CD8+ T cells in human hepatitis C virus (HCV) infection before and after treatment.

SARS-CoV-2 Specific T Cell Responses Are Lower in Children and Increase with Age and Time after Infection

[Nature Communications] Scientists reported SARS-CoV-2 specific T cell responses in infected adults and children and find that the acute and memory CD4+ T cell responses to structural SARS-CoV-2 proteins increase with age, whereas CD8+ T cell responses increase with time post-infection.

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