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T cells

Single-Cell RNA Sequencing Reveals Ex Vivo Signatures of SARS-CoV-2-Reactive T Cells through ‘Reverse Phenotyping’

[Nature Communications] Investigators used single-cell RNA sequencing to identify and profile SARS-CoV-2-reactive T cells from COVID-19 patients.

Epigenetic Scars of CD8+ T Cell Exhaustion Persist after Cure of Chronic Infection in Humans

[Nature Immunology] Researchers showed that the epigenetic state of exhaustion was largely irreversible, even after curative therapy. Analysis of chromatin accessibility in HCV- and HIV-specific responses identified a core epigenetic program of exhaustion in CD8+ T cells, which underwent only limited remodeling before and after resolution of infection.

Mucosal Vaccines – Fortifying the Frontiers

[Nature Reviews Immunology] Mucosal vaccines offer the potential to trigger robust protective immune responses at the predominant sites of pathogen infection. The identification of safe and effective mucosal adjuvants allied to innovative antigen discovery and delivery strategies is key to advancing mucosal vaccines.

Diagnostic Potential of Serum Extracellular Vesicles Expressing Prostate-Specific Membrane Antigen in Urologic Malignancies

[Scientific Reports] Investigators developed a sandwich ELISA to detect prostate-specific membrane antigen on small extracellular vesicles (EVs) using T-cell immunoglobulin domain and mucin domain-containing protein 4 as a capture molecule for EVs and to evaluate its diagnostic potential in urologic malignancies.

Eureka Therapeutics Announces Initiation of Phase I/II ARYA-3 Clinical Trial of GPC3 Targeting ARTEMIS® T Cell Therapy in Liver Cancer

[Eureka Therapeutics, Inc.] Eureka Therapeutics, Inc. announced the initiation of a Phase I/II clinical trial of ECT204, a GPC3 targeting ARTEMIS® T-cell therapy for the treatment of hepatocellular carcinoma, the predominant type of liver cancer.

Whole-Genome Analysis of TET Dioxygenase Function in Regulatory T Cells

[EMBO Reports] Investigators used whole-genome analyses to show that the transcriptional program and epigenetic features of Treg cells were attenuated in the absence of Tet2 and Tet3.

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